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2026-06-12 16:38 1mo ago
2026-04-16 07:57 3mo ago
Here Are Thursday’s Top Wall Street Analyst Research Calls: Autoliv, CoreWeave, Corning, Dicks Sporting Goods, Federated Hermes, Gitlab, PayPal, Pfizer, Okta, and More
EQH Axa Equitable Holdings
FMP Stock News
Original source text
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© robertcicchetti / Getty Images

Pre-Market Stock Futures: The futures are trading modestly higher after a wild Wednesday that saw the Nasdaq explode higher to close at an all-time high of 24,016, up a hefty 1.60%, while the S&P 500 closed up 0.80% at 7,022, also hitting a brand-new all-time closing high. The small-cap Russell 2000, the leading index this year, finished the day at 2,713, up 0.30%, while the Dow Jones Industrial Average was the only loser, closing at 48,463, down 0.15%. Analysts cited more solid news on the war and positive earnings results from the mega-cap money-center banks and brokerage firms.

Treasury Bonds: The sellers showed up on Wednesday as yields rose across the Treasury curve, and this was no surprise after the big rally in U.S. sovereign debt on Tuesday. With the prospect of interest rate cuts falling, Treasury Secretary Scott Bessent said that while he remains constructive on rate cuts in 2026, they may need to be moved out to later in the year. The 30-year-long bond closed Wednesday at 4.89%, while the benchmark 10-year note was last seen at 4.28%.

Oil and Gas: After some heavy selling across the energy complex on Tuesday, the major benchmarks finished modestly higher on Wednesday. Brent Crude closed at $94.94, up 0.16%, while West Texas Intermediate closed virtually unchanged at $91.29. Natural gas closed the session at $2.61, up 0.41% 

Gold: After a big day on Tuesday for the precious metals, like oil and energy stocks, the sellers emerged on Wednesday, and prices for the top metals both closed lower. Gold was last seen at $4,790, down 1.03%, while the final trade for Silver was reported at $78.86, down 0.69%. The strength in the U.S. dollar was cited as a major reason for the decline, and profit-taking after the strong move over the last week was also a likely culprit.

Crypto: The cryptocurrency markets saw a slight correction yesterday following some big early-week gains, with Bitcoin holding above $74,000. Despite volatility driven by geopolitical tensions, Bitcoin, Ethereum, and some other altcoins remained relatively stable. Needless to say, crypto traders and strategists are monitoring the Middle East, where tensions are influencing price movements, though Bitcoin and Ethereum remain up significantly since the conflict began. At 8 AM EDT, Bitcoin is trading at $74,440, while Ethereum is quoted at $2,333.

24/7 Wall St. reviews dozens of analyst research reports daily to identify new investment ideas for both investors and traders. Some of these daily analyst calls cover stocks to buy. Other calls cover stocks to sell or avoid. Remember that no single analyst call should ever be used as a basis to buy or sell a stock. 

Here are some of the top Wall Street analyst upgrades, downgrades, and initiations seen on Thursday, April 16, 2026. 

Upgrades: Blackstone Mortgage Trust Inc. (NYSE: BXMT) | BXMT Price Prediction was upgraded to Overweight from Neutral at JPMorgan, with a $21 target price for the shares. Bread Financial Holdings Inc. (NYSE: BFH) was upgraded to Equal Weight from Underweight at Morgan Stanley, with a $91 target price. Equitable Holdings Inc. (NYSE: EQH) was upgraded to Strong Buy from Market Perform at Raymond James, which has a $58 target price for the stock. Grupo Aeroportuario del Centro Norte SAB De CV (NASDAQ: OMAB) was raised to Buy from Hold at HSBC, with a $134 target price for the company. Okta Inc. (NASDAQ: OKTA) was upgraded to Outperform from Market Perform at Raymond James, which has an $85 target price. Downgrades: Corning Inc. (NYSE: GLW) was downgraded to Neutral from Overweight at JPMorgan, which actually raised the target price for the fiber and display giant to $175 from $115. Federated Hermes Inc. (NYSE: FHI) was downgraded to Underweight from Neutral at JPMorgan, which nudged the price target to $56 from $55. GitLab Inc. (NASDAQ: GTLB) was cut to Neutral from Buy at UBS, which slashed the target price for the stock to $24 from $44. PayPal Holdings Inc. (NASDAQ: PYPL) was downgraded to Neutral from Outperform at Mizuho, which cut the target price for the stock to $50 from $60. Two Harbors Investment Corp. (NYSE: TWO) was downgraded to Underweight from Neutral at JPMorgan, which trimmed the target price for the stock to $11 from $12.50. Initiations: Autoliv Inc. (NYSE: ALV) was initiated with a Buy rating at Bank of America, with a $140 price target. CoreWeave (NASDAQ: CRWV) was started with an Outperform rating at Wolfe Research, which has a $150 target price objective. Dicks Sporting Goods Inc. (NYSE: DKS) was initiated with a Buy rating at BTIG, which has a $300 target price for the retail giant. Equifax Inc. (NYSE: EFX) was initiated with an Overweight rating at Mizuho, which has a $222 target price for the shares. Pfizer Inc. (NYSE: PFE) was initiated with an Outperform rating at CICC, which has a $33 target for the healthcare giant.
2026-06-12 16:38 1mo ago
2026-04-18 04:13 3mo ago
Equitable Holdings, Inc. $EQH Shares Purchased by Benson Investment Management Company Inc.
EQH Axa Equitable Holdings
FMP Stock News
Original source text
Posted by Defense World Staff on Apr 18th, 2026

Benson Investment Management Company Inc. boosted its holdings in Equitable Holdings, Inc. (NYSE:EQH – Free Report) by 15.5% in the fourth quarter, according to the company in its most recent Form 13F filing with the Securities and Exchange Commission (SEC). The firm owned 120,375 shares of the company’s stock after purchasing an additional 16,133 shares during the quarter. Benson Investment Management Company Inc.’s holdings in Equitable were worth $5,736,000 at the end of the most recent quarter.

Other hedge funds have also recently added to or reduced their stakes in the company. Johnson Financial Group Inc. acquired a new stake in Equitable in the third quarter worth approximately $26,000. Root Financial Partners LLC acquired a new stake in Equitable in the 3rd quarter valued at about $36,000. Hilltop National Bank acquired a new stake in shares of Equitable during the 3rd quarter valued at $37,000. Caitong International Asset Management Co. Ltd acquired a new stake in shares of Equitable during the 3rd quarter valued at $38,000. Finally, Geneos Wealth Management Inc. lifted its position in shares of Equitable by 92.6% during the 1st quarter. Geneos Wealth Management Inc. now owns 882 shares of the company’s stock valued at $46,000 after acquiring an additional 424 shares during the last quarter. Institutional investors and hedge funds own 92.70% of the company’s stock.

Analysts Set New Price Targets EQH has been the subject of a number of analyst reports. Zacks Research lowered shares of Equitable from a “hold” rating to a “strong sell” rating in a research note on Thursday, January 22nd. Weiss Ratings cut shares of Equitable from a “hold (c-)” rating to a “sell (d+)” rating in a report on Monday, March 2nd. Wells Fargo & Company reduced their target price on Equitable from $57.00 to $56.00 and set an “overweight” rating for the company in a report on Friday, April 10th. Wall Street Zen upgraded Equitable from a “sell” rating to a “hold” rating in a report on Saturday, February 28th. Finally, UBS Group reduced their price target on shares of Equitable from $66.00 to $58.00 and set a “buy” rating for the company in a research report on Thursday, April 9th. Two analysts have rated the stock with a Strong Buy rating, nine have issued a Buy rating and two have issued a Sell rating to the company’s stock. According to data from MarketBeat.com, the stock currently has an average rating of “Moderate Buy” and an average price target of $56.91.

View Our Latest Report on Equitable

Equitable Trading Down 0.7% Shares of Equitable stock opened at $41.68 on Friday. The firm has a market capitalization of $11.69 billion, a PE ratio of -8.65, a price-to-earnings-growth ratio of 0.40 and a beta of 1.11. The company has a debt-to-equity ratio of 16.42, a current ratio of 0.13 and a quick ratio of 0.13. The company’s fifty day moving average price is $39.98 and its two-hundred day moving average price is $44.72. Equitable Holdings, Inc. has a 52-week low of $35.19 and a 52-week high of $56.61.

Equitable Announces Dividend The business also recently announced a quarterly dividend, which was paid on Wednesday, March 11th. Stockholders of record on Wednesday, March 4th were issued a $0.27 dividend. The ex-dividend date of this dividend was Wednesday, March 4th. This represents a $1.08 dividend on an annualized basis and a dividend yield of 2.6%. Equitable’s dividend payout ratio is presently -22.41%.

Equitable declared that its Board of Directors has initiated a stock repurchase plan on Wednesday, February 11th that allows the company to repurchase $1.00 billion in outstanding shares. This repurchase authorization allows the company to buy up to 7.7% of its shares through open market purchases. Shares repurchase plans are often a sign that the company’s management believes its shares are undervalued.

Insider Transactions at Equitable In other news, CEO Mark Pearson sold 39,700 shares of the stock in a transaction that occurred on Tuesday, January 20th. The stock was sold at an average price of $46.20, for a total value of $1,834,140.00. Following the completion of the transaction, the chief executive officer directly owned 652,945 shares of the company’s stock, valued at approximately $30,166,059. This represents a 5.73% decrease in their position. The sale was disclosed in a filing with the SEC, which is accessible through the SEC website. Also, COO Jeffrey J. Hurd sold 14,358 shares of the company’s stock in a transaction dated Wednesday, April 15th. The stock was sold at an average price of $40.58, for a total transaction of $582,647.64. Following the completion of the sale, the chief operating officer directly owned 84,403 shares in the company, valued at approximately $3,425,073.74. The trade was a 14.54% decrease in their position. The disclosure for this sale is available in the SEC filing. The transaction was executed under a pre-arranged Rule 10b5-1 trading plan. In the last ninety days, insiders sold 128,116 shares of company stock valued at $5,386,439. Corporate insiders own 1.10% of the company’s stock.

Key Stories Impacting Equitable Here are the key news stories impacting Equitable this week:

Positive Sentiment: Raymond James upgraded EQH from “market perform” to “strong-buy” with a $58 price target (implying ~39% upside from current levels), which is a clear bullish catalyst for investors. Raymond James Upgrade Positive Sentiment: Management and counterpart Corebridge have discussed potential share buybacks ahead of the pending Corebridge–Equitable transaction; buyback talk typically supports the share price by reducing float and signaling confidence in valuation. Buybacks & Merger Discussion Neutral Sentiment: Insider sales disclosed (all executed under pre-arranged Rule 10b5‑1 plans): COO Jeffrey Hurd sold 14,358 shares (~$40.58 avg), Nick Lane sold 10,000 shares (~$40.44 avg), and CEO Mark Pearson sold 1,387 shares (~$40.03 avg). Because these were planned 10b5‑1 trades the market impact is muted, but such filings can still raise short-term selling pressure. Filing links: Hurd SEC Filing Lane SEC Filing Pearson SEC Filing Negative Sentiment: Technical and fundamental headwinds: the 50‑day moving average (~$40.06) sits below the 200‑day (~$44.79) and key metrics show negative earnings (negative P/E) and high reported leverage; these factors can limit upside and contribute to continued selling pressure despite positive headlines. About Equitable (Free Report)

Equitable Holdings, Inc (NYSE: EQH) is a leading provider of life insurance, annuities and retirement plan services in the United States. Through its insurance subsidiary, AXA Equitable Life Insurance Company, the firm offers a broad range of permanent and term life insurance products designed to help individuals and families manage risk and build wealth. In addition, Equitable provides fixed, variable and indexed annuity solutions to support income planning in retirement, as well as a suite of group retirement and pension plan services for employers and plan sponsors.

The company also maintains an asset management arm that delivers investment strategies across equities, fixed income and alternative asset classes for both retail and institutional clients.

See Also Five stocks we like better than Equitable

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2026-06-12 16:38 1mo ago
2026-04-19 04:36 3mo ago
Jeffrey Hurd Sells 14,358 Shares of Equitable (NYSE:EQH) Stock
EQH Axa Equitable Holdings
FMP Stock News
Original source text
Posted by Defense World Staff on Apr 19th, 2026

Equitable Holdings, Inc. (NYSE:EQH – Get Free Report) COO Jeffrey Hurd sold 14,358 shares of the company’s stock in a transaction dated Wednesday, April 15th. The stock was sold at an average price of $40.58, for a total transaction of $582,647.64. Following the completion of the sale, the chief operating officer directly owned 84,403 shares of the company’s stock, valued at $3,425,073.74. The trade was a 14.54% decrease in their ownership of the stock. The sale was disclosed in a filing with the SEC, which can be accessed through this link. The transaction was executed under a pre-arranged Rule 10b5-1 trading plan.

Equitable Trading Down 0.7% Shares of EQH stock opened at $41.68 on Friday. Equitable Holdings, Inc. has a 52-week low of $35.19 and a 52-week high of $56.61. The company has a debt-to-equity ratio of 16.42, a quick ratio of 0.13 and a current ratio of 0.13. The company has a 50-day simple moving average of $39.98 and a two-hundred day simple moving average of $44.67. The company has a market capitalization of $11.69 billion, a price-to-earnings ratio of -8.65, a PEG ratio of 0.40 and a beta of 1.11.

Equitable announced that its Board of Directors has initiated a share buyback program on Wednesday, February 11th that permits the company to repurchase $1.00 billion in shares. This repurchase authorization permits the company to purchase up to 7.7% of its shares through open market purchases. Shares repurchase programs are often a sign that the company’s board believes its stock is undervalued.

Equitable Announces Dividend The company also recently disclosed a quarterly dividend, which was paid on Wednesday, March 11th. Shareholders of record on Wednesday, March 4th were given a $0.27 dividend. This represents a $1.08 dividend on an annualized basis and a yield of 2.6%. The ex-dividend date of this dividend was Wednesday, March 4th. Equitable’s dividend payout ratio is presently -22.41%.

Analyst Upgrades and Downgrades EQH has been the subject of a number of research reports. UBS Group reduced their target price on shares of Equitable from $66.00 to $58.00 and set a “buy” rating for the company in a research report on Thursday, April 9th. JPMorgan Chase & Co. reduced their target price on shares of Equitable from $60.00 to $58.00 and set an “overweight” rating for the company in a research report on Thursday, February 5th. Barclays reduced their target price on shares of Equitable from $57.00 to $49.00 and set an “overweight” rating for the company in a research report on Wednesday, April 8th. The Goldman Sachs Group set a $60.00 target price on shares of Equitable in a research report on Monday, January 5th. Finally, Mizuho reduced their target price on shares of Equitable from $65.00 to $58.00 and set an “outperform” rating for the company in a research report on Monday, April 13th. Two research analysts have rated the stock with a Strong Buy rating, nine have given a Buy rating and two have issued a Sell rating to the company’s stock. Based on data from MarketBeat.com, Equitable currently has an average rating of “Moderate Buy” and an average price target of $56.91.

Get Our Latest Report on EQH

Institutional Inflows and Outflows Several institutional investors and hedge funds have recently bought and sold shares of the business. Parkside Financial Bank & Trust boosted its holdings in Equitable by 9.1% in the 4th quarter. Parkside Financial Bank & Trust now owns 2,726 shares of the company’s stock worth $130,000 after buying an additional 227 shares during the period. Steward Partners Investment Advisory LLC boosted its holdings in Equitable by 9.1% in the 4th quarter. Steward Partners Investment Advisory LLC now owns 2,999 shares of the company’s stock worth $143,000 after buying an additional 249 shares during the period. Wilmington Savings Fund Society FSB boosted its holdings in Equitable by 11.7% in the 3rd quarter. Wilmington Savings Fund Society FSB now owns 2,634 shares of the company’s stock worth $134,000 after buying an additional 275 shares during the period. Farther Finance Advisors LLC boosted its holdings in Equitable by 12.4% in the 4th quarter. Farther Finance Advisors LLC now owns 2,882 shares of the company’s stock worth $137,000 after buying an additional 317 shares during the period. Finally, Clearstead Advisors LLC boosted its holdings in Equitable by 1.3% in the 4th quarter. Clearstead Advisors LLC now owns 25,926 shares of the company’s stock worth $1,235,000 after buying an additional 329 shares during the period. 92.70% of the stock is owned by institutional investors.

Key Equitable News Here are the key news stories impacting Equitable this week:

Positive Sentiment: Raymond James upgraded EQH from “market perform” to “strong-buy” with a $58 price target (implying ~39% upside from current levels), which is a clear bullish catalyst for investors. Raymond James Upgrade Positive Sentiment: Management and counterpart Corebridge have discussed potential share buybacks ahead of the pending Corebridge–Equitable transaction; buyback talk typically supports the share price by reducing float and signaling confidence in valuation. Buybacks & Merger Discussion Neutral Sentiment: Insider sales disclosed (all executed under pre-arranged Rule 10b5‑1 plans): COO Jeffrey Hurd sold 14,358 shares (~$40.58 avg), Nick Lane sold 10,000 shares (~$40.44 avg), and CEO Mark Pearson sold 1,387 shares (~$40.03 avg). Because these were planned 10b5‑1 trades the market impact is muted, but such filings can still raise short-term selling pressure. Filing links: Hurd SEC Filing Lane SEC Filing Pearson SEC Filing Negative Sentiment: Technical and fundamental headwinds: the 50‑day moving average (~$40.06) sits below the 200‑day (~$44.79) and key metrics show negative earnings (negative P/E) and high reported leverage; these factors can limit upside and contribute to continued selling pressure despite positive headlines. Equitable Company Profile (Get Free Report)

Equitable Holdings, Inc (NYSE: EQH) is a leading provider of life insurance, annuities and retirement plan services in the United States. Through its insurance subsidiary, AXA Equitable Life Insurance Company, the firm offers a broad range of permanent and term life insurance products designed to help individuals and families manage risk and build wealth. In addition, Equitable provides fixed, variable and indexed annuity solutions to support income planning in retirement, as well as a suite of group retirement and pension plan services for employers and plan sponsors.

The company also maintains an asset management arm that delivers investment strategies across equities, fixed income and alternative asset classes for both retail and institutional clients.

Featured Stories Five stocks we like better than Equitable

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2026-06-12 16:37 1mo ago
2026-04-19 04:36 3mo ago
Nick Lane Sells 10,000 Shares of Equitable (NYSE:EQH) Stock
EQH Axa Equitable Holdings
FMP Stock News
Original source text
Posted by Defense World Staff on Apr 19th, 2026

Equitable Holdings, Inc. (NYSE:EQH – Get Free Report) insider Nick Lane sold 10,000 shares of the company’s stock in a transaction dated Wednesday, April 15th. The shares were sold at an average price of $40.44, for a total transaction of $404,400.00. Following the sale, the insider directly owned 124,218 shares of the company’s stock, valued at $5,023,375.92. This represents a 7.45% decrease in their ownership of the stock. The transaction was disclosed in a filing with the SEC, which is accessible through this link. The transaction was executed under a pre-arranged Rule 10b5-1 trading plan.

Nick Lane also recently made the following trade(s):

On Wednesday, April 8th, Nick Lane sold 10,000 shares of Equitable stock. The shares were sold at an average price of $40.04, for a total transaction of $400,400.00. Equitable Price Performance EQH stock opened at $41.68 on Friday. The company has a current ratio of 0.13, a quick ratio of 0.13 and a debt-to-equity ratio of 16.42. Equitable Holdings, Inc. has a one year low of $35.19 and a one year high of $56.61. The firm has a market capitalization of $11.69 billion, a PE ratio of -8.65, a P/E/G ratio of 0.40 and a beta of 1.11. The firm has a 50-day moving average of $39.98 and a two-hundred day moving average of $44.67.

Equitable announced that its board has approved a share repurchase plan on Wednesday, February 11th that permits the company to buyback $1.00 billion in shares. This buyback authorization permits the company to purchase up to 7.7% of its shares through open market purchases. Shares buyback plans are typically a sign that the company’s management believes its shares are undervalued.

Equitable Announces Dividend The company also recently disclosed a quarterly dividend, which was paid on Wednesday, March 11th. Shareholders of record on Wednesday, March 4th were paid a dividend of $0.27 per share. The ex-dividend date of this dividend was Wednesday, March 4th. This represents a $1.08 dividend on an annualized basis and a yield of 2.6%. Equitable’s dividend payout ratio is currently -22.41%.

Hedge Funds Weigh In On Equitable Hedge funds have recently added to or reduced their stakes in the company. Johnson Financial Group Inc. acquired a new position in Equitable in the third quarter worth approximately $26,000. Root Financial Partners LLC acquired a new position in Equitable during the third quarter valued at approximately $36,000. Hilltop National Bank acquired a new position in Equitable during the third quarter valued at approximately $37,000. Covestor Ltd grew its holdings in Equitable by 124.7% during the fourth quarter. Covestor Ltd now owns 728 shares of the company’s stock valued at $35,000 after purchasing an additional 404 shares during the last quarter. Finally, Caitong International Asset Management Co. Ltd acquired a new position in Equitable during the third quarter valued at approximately $38,000. Institutional investors and hedge funds own 92.70% of the company’s stock.

Key Headlines Impacting Equitable Here are the key news stories impacting Equitable this week:

Positive Sentiment: Raymond James upgraded EQH from “market perform” to “strong-buy” with a $58 price target (implying ~39% upside from current levels), which is a clear bullish catalyst for investors. Raymond James Upgrade Positive Sentiment: Management and counterpart Corebridge have discussed potential share buybacks ahead of the pending Corebridge–Equitable transaction; buyback talk typically supports the share price by reducing float and signaling confidence in valuation. Buybacks & Merger Discussion Neutral Sentiment: Insider sales disclosed (all executed under pre-arranged Rule 10b5‑1 plans): COO Jeffrey Hurd sold 14,358 shares (~$40.58 avg), Nick Lane sold 10,000 shares (~$40.44 avg), and CEO Mark Pearson sold 1,387 shares (~$40.03 avg). Because these were planned 10b5‑1 trades the market impact is muted, but such filings can still raise short-term selling pressure. Filing links: Hurd SEC Filing Lane SEC Filing Pearson SEC Filing Negative Sentiment: Technical and fundamental headwinds: the 50‑day moving average (~$40.06) sits below the 200‑day (~$44.79) and key metrics show negative earnings (negative P/E) and high reported leverage; these factors can limit upside and contribute to continued selling pressure despite positive headlines. Analysts Set New Price Targets A number of analysts have commented on the stock. Wall Street Zen raised shares of Equitable from a “sell” rating to a “hold” rating in a research note on Saturday, February 28th. JPMorgan Chase & Co. reduced their price target on shares of Equitable from $60.00 to $58.00 and set an “overweight” rating for the company in a research report on Thursday, February 5th. The Goldman Sachs Group set a $60.00 price target on shares of Equitable in a research report on Monday, January 5th. Weiss Ratings lowered shares of Equitable from a “hold (c-)” rating to a “sell (d+)” rating in a research report on Monday, March 2nd. Finally, Morgan Stanley reduced their price target on shares of Equitable from $59.00 to $54.00 and set an “overweight” rating for the company in a research report on Tuesday, March 3rd. Two research analysts have rated the stock with a Strong Buy rating, nine have assigned a Buy rating and two have assigned a Sell rating to the company. According to data from MarketBeat.com, the stock currently has an average rating of “Moderate Buy” and a consensus price target of $56.91.

Check Out Our Latest Stock Analysis on Equitable

Equitable Company Profile (Get Free Report)

Equitable Holdings, Inc (NYSE: EQH) is a leading provider of life insurance, annuities and retirement plan services in the United States. Through its insurance subsidiary, AXA Equitable Life Insurance Company, the firm offers a broad range of permanent and term life insurance products designed to help individuals and families manage risk and build wealth. In addition, Equitable provides fixed, variable and indexed annuity solutions to support income planning in retirement, as well as a suite of group retirement and pension plan services for employers and plan sponsors.

The company also maintains an asset management arm that delivers investment strategies across equities, fixed income and alternative asset classes for both retail and institutional clients.

See Also Five stocks we like better than Equitable

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2026-06-12 16:37 1mo ago
2026-04-21 08:00 3mo ago
TechPoint Youth Receives $200,000 Grant to Expand Equitable STEM Access Across Indiana
EQH Axa Equitable Holdings
FMP Stock News
Original source text
Funding will support robotics education and community engagement for underserved students statewide

INDIANAPOLIS--(BUSINESS WIRE)--TechPoint Youth today announced it has received a $200,000 grant from the Global Technology Industry Association (GTIA) to support the expansion of equitable robotics and STEM programming across Indiana. The funding will help TechPoint Youth reach an additional 10,000 Indiana students, particularly girls, students of color, and youth in under-resourced rural and urban communities, while strengthening educator training and local STEM infrastructure.

Indiana is home to a growing technology economy. Through TechPoint Youth's robotics initiative, STEM Mentor and Xplore programs, the organization has proven that access to hands-on technology education changes student trajectories.

Share Founded to equip and empower the next generation of STEM leaders, TechPoint Youth works to expand equitable access to high-impact robotics and technology education statewide. The funding from GTIA will strengthen those efforts by enabling the organization to deepen its reach into communities that have historically had the least access to quality STEM programming, closing gaps in opportunity and building a more inclusive pipeline of future tech leaders in Indiana.

"This investment from GTIA is a powerful affirmation of what we already know to be true, that every young person deserves the chance to discover their potential and find passion for a future career in STEM," said Jamie Inskeep, President and CEO of TechPoint Youth. "With this funding, we can go further and reach deeper into the communities that need us most. We're grateful to GTIA and its members for recognizing that expanding access to STEM isn't just beneficial for the students themselves, it's also fundamental for developing Indiana's future workforce."

TechPoint Youth is one of 45 nonprofit organizations worldwide to have received a GTIA grant as part of the association's $1.91 million in total charitable giving in 2025. GTIA's charitable investment reinforces the association's commitment to advancing access, equity, education, workforce development, and technology-driven innovation. GTIA has recently announced it is expanding its charitable giving to $5 million in 2026.

Through a significantly expanded philanthropic portfolio, GTIA directed funding and resources to organizations such as TechPoint Youth who are creating measurable social impact across education, healthcare, workforce readiness, and community development.

"Philanthropy has long been central to GTIA's mission," said Kelly Ricker, chief operating officer of GTIA. "In 2025, our members helped us take decisive steps to scale our impact – investing in organizations that use technology to expand opportunities, promote equity and create lasting change. Every advancement we make in our giving programs is driven by the commitment and shared purpose of our member community. Their leadership ensures that innovation truly benefits communities worldwide."

Indiana is home to a growing technology economy, and TechPoint Youth sits at the center of building the workforce that will power it. Through its robotics initiative, STEM Mentor and Xplore programs, and community partnerships, TechPoint Youth has spent years proving that access to hands-on technology K-12 education changes trajectories. This GTIA grant will allow the organization to scale, bringing students into the fold, training more educators, and ensuring that the communities with the most to gain from STEM aren't left behind.

About TechPoint Youth TechPoint Youth is Indiana's leading nonprofit dedicated to inspiring and empowering the next generation of STEM leaders by expanding equitable access to high-impact robotics and technology education statewide. For more information, visit techpointyouth.org.

About the Global Technology Industry Association The Global Technology Industry Association (GTIA) is the only vendor-neutral, 501(c)(6) nonprofit membership community connecting and representing the worldwide IT channel. For more information, visit gtia.org.
2026-06-12 16:37 1mo ago
2026-04-27 05:07 3mo ago
Mirae Asset Global Investments Co. Ltd. Trims Stock Position in Equitable Holdings, Inc. $EQH
EQH Axa Equitable Holdings
FMP Stock News
Original source text
Mirae Asset Global Investments Co. Ltd. decreased its stake in Equitable Holdings, Inc. (NYSE:EQH – Free Report) by 92.7% in the 4th quarter, according to the company in its most recent filing with the Securities and Exchange Commission. The institutional investor owned 3,908 shares of the company’s stock after selling 49,959 shares during the period. Mirae Asset Global Investments Co. Ltd.’s holdings in Equitable were worth $186,000 at the end of the most recent reporting period.

A number of other hedge funds have also recently modified their holdings of EQH. Capital International Investors lifted its position in Equitable by 49.5% in the third quarter. Capital International Investors now owns 11,012,837 shares of the company’s stock valued at $559,232,000 after acquiring an additional 3,645,301 shares during the last quarter. Thornburg Investment Management Inc. grew its holdings in shares of Equitable by 0.3% during the third quarter. Thornburg Investment Management Inc. now owns 4,867,643 shares of the company’s stock worth $247,179,000 after purchasing an additional 12,370 shares during the last quarter. Massachusetts Financial Services Co. MA grew its holdings in shares of Equitable by 4.2% during the fourth quarter. Massachusetts Financial Services Co. MA now owns 4,822,908 shares of the company’s stock worth $229,812,000 after purchasing an additional 193,640 shares during the last quarter. Pzena Investment Management LLC increased its position in shares of Equitable by 1.3% during the third quarter. Pzena Investment Management LLC now owns 4,297,008 shares of the company’s stock worth $218,202,000 after purchasing an additional 55,798 shares in the last quarter. Finally, Boston Partners lifted its holdings in shares of Equitable by 2.0% in the 3rd quarter. Boston Partners now owns 3,637,414 shares of the company’s stock valued at $184,704,000 after purchasing an additional 72,267 shares during the last quarter. 92.70% of the stock is owned by hedge funds and other institutional investors.

Insider Activity In other news, COO Jeffrey J. Hurd sold 14,358 shares of the business’s stock in a transaction that occurred on Wednesday, April 8th. The stock was sold at an average price of $40.04, for a total value of $574,894.32. Following the transaction, the chief operating officer owned 89,403 shares of the company’s stock, valued at approximately $3,579,696.12. The trade was a 13.84% decrease in their ownership of the stock. The transaction was disclosed in a document filed with the SEC, which is accessible through this hyperlink. The transaction was executed under a pre-arranged Rule 10b5-1 trading plan. Also, insider Nick Lane sold 10,000 shares of the stock in a transaction on Wednesday, April 15th. The stock was sold at an average price of $40.44, for a total value of $404,400.00. Following the sale, the insider directly owned 124,218 shares of the company’s stock, valued at approximately $5,023,375.92. This represents a 7.45% decrease in their ownership of the stock. Additional details regarding this sale are available in the official SEC disclosure. The transaction was executed under a pre-arranged Rule 10b5-1 trading plan. Over the last 90 days, insiders have sold 128,116 shares of company stock valued at $5,205,010. Company insiders own 1.10% of the company’s stock.

Equitable Stock Performance NYSE EQH opened at $41.17 on Monday. The firm has a market cap of $11.59 billion, a P/E ratio of -8.54, a P/E/G ratio of 0.39 and a beta of 1.11. Equitable Holdings, Inc. has a 52-week low of $35.19 and a 52-week high of $56.61. The business’s 50-day moving average price is $39.64 and its 200 day moving average price is $44.31. The company has a quick ratio of 0.13, a current ratio of 0.13 and a debt-to-equity ratio of 16.42.

Equitable announced that its Board of Directors has authorized a stock buyback plan on Wednesday, February 11th that permits the company to repurchase $1.00 billion in outstanding shares. This repurchase authorization permits the company to buy up to 7.7% of its shares through open market purchases. Shares repurchase plans are typically an indication that the company’s leadership believes its shares are undervalued.

Equitable Announces Dividend The business also recently announced a quarterly dividend, which was paid on Wednesday, March 11th. Shareholders of record on Wednesday, March 4th were paid a $0.27 dividend. This represents a $1.08 annualized dividend and a dividend yield of 2.6%. The ex-dividend date was Wednesday, March 4th. Equitable’s dividend payout ratio (DPR) is -22.41%.

Analyst Upgrades and Downgrades A number of analysts recently issued reports on EQH shares. Keefe, Bruyette & Woods decreased their target price on Equitable from $53.00 to $51.00 and set an “outperform” rating for the company in a research report on Friday, April 10th. Morgan Stanley reduced their price objective on Equitable from $59.00 to $54.00 and set an “overweight” rating for the company in a research note on Tuesday, March 3rd. Barclays decreased their price objective on Equitable from $57.00 to $49.00 and set an “overweight” rating for the company in a report on Wednesday, April 8th. Wells Fargo & Company lowered their target price on shares of Equitable from $57.00 to $56.00 and set an “overweight” rating on the stock in a research report on Friday, April 10th. Finally, The Goldman Sachs Group set a $60.00 target price on shares of Equitable in a report on Monday, January 5th. Two research analysts have rated the stock with a Strong Buy rating, nine have given a Buy rating and two have issued a Sell rating to the company’s stock. According to data from MarketBeat, the stock presently has an average rating of “Moderate Buy” and an average target price of $56.91.

Check Out Our Latest Research Report on EQH

Equitable Company Profile (Free Report)

Equitable Holdings, Inc (NYSE: EQH) is a leading provider of life insurance, annuities and retirement plan services in the United States. Through its insurance subsidiary, AXA Equitable Life Insurance Company, the firm offers a broad range of permanent and term life insurance products designed to help individuals and families manage risk and build wealth. In addition, Equitable provides fixed, variable and indexed annuity solutions to support income planning in retirement, as well as a suite of group retirement and pension plan services for employers and plan sponsors.

The company also maintains an asset management arm that delivers investment strategies across equities, fixed income and alternative asset classes for both retail and institutional clients.

Featured Stories Five stocks we like better than Equitable Want to see what other hedge funds are holding EQH? Visit HoldingsChannel.com to get the latest 13F filings and insider trades for Equitable Holdings, Inc. (NYSE:EQH – Free Report).

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2026-06-12 16:37 1mo ago
2026-04-27 11:02 3mo ago
Equitable Holdings, Inc. (EQH) Earnings Expected to Grow: What to Know Ahead of Next Week's Release
EQH Axa Equitable Holdings
FMP Stock News
Original source text
The market expects Equitable Holdings, Inc. (EQH - Free Report) to deliver a year-over-year increase in earnings on higher revenues when it reports results for the quarter ended March 2026. This widely-known consensus outlook is important in assessing the company's earnings picture, but a powerful factor that might influence its near-term stock price is how the actual results compare to these estimates.

The earnings report, which is expected to be released on May 4, might help the stock move higher if these key numbers are better than expectations. On the other hand, if they miss, the stock may move lower.

While the sustainability of the immediate price change and future earnings expectations will mostly depend on management's discussion of business conditions on the earnings call, it's worth handicapping the probability of a positive EPS surprise.

Zacks Consensus EstimateThis company is expected to post quarterly earnings of $1.63 per share in its upcoming report, which represents a year-over-year change of +20.7%.

Revenues are expected to be $4.01 billion, up 5.9% from the year-ago quarter.

Estimate Revisions TrendThe consensus EPS estimate for the quarter has been revised 3.5% lower over the last 30 days to the current level. This is essentially a reflection of how the covering analysts have collectively reassessed their initial estimates over this period.

Investors should keep in mind that the direction of estimate revisions by each of the covering analysts may not always get reflected in the aggregate change.

Price, Consensus and EPS Surprise

Earnings WhisperEstimate revisions ahead of a company's earnings release offer clues to the business conditions for the period whose results are coming out. Our proprietary surprise prediction model -- the Zacks Earnings ESP (Expected Surprise Prediction) -- has this insight at its core.

The Zacks Earnings ESP compares the Most Accurate Estimate to the Zacks Consensus Estimate for the quarter; the Most Accurate Estimate is a more recent version of the Zacks Consensus EPS estimate. The idea here is that analysts revising their estimates right before an earnings release have the latest information, which could potentially be more accurate than what they and others contributing to the consensus had predicted earlier.

Thus, a positive or negative Earnings ESP reading theoretically indicates the likely deviation of the actual earnings from the consensus estimate. However, the model's predictive power is significant for positive ESP readings only.

A positive Earnings ESP is a strong predictor of an earnings beat, particularly when combined with a Zacks Rank #1 (Strong Buy), 2 (Buy) or 3 (Hold). Our research shows that stocks with this combination produce a positive surprise nearly 70% of the time, and a solid Zacks Rank actually increases the predictive power of Earnings ESP.

Please note that a negative Earnings ESP reading is not indicative of an earnings miss. Our research shows that it is difficult to predict an earnings beat with any degree of confidence for stocks with negative Earnings ESP readings and/or Zacks Rank of 4 (Sell) or 5 (Strong Sell).

How Have the Numbers Shaped Up for Equitable Holdings?For Equitable Holdings, the Most Accurate Estimate is the same as the Zacks Consensus Estimate, suggesting that there are no recent analyst views which differ from what have been considered to derive the consensus estimate. This has resulted in an Earnings ESP of 0%.

On the other hand, the stock currently carries a Zacks Rank of #4.

So, this combination makes it difficult to conclusively predict that Equitable Holdings will beat the consensus EPS estimate.

Does Earnings Surprise History Hold Any Clue?While calculating estimates for a company's future earnings, analysts often consider to what extent it has been able to match past consensus estimates. So, it's worth taking a look at the surprise history for gauging its influence on the upcoming number.

For the last reported quarter, it was expected that Equitable Holdings would post earnings of $1.75 per share when it actually produced earnings of $1.76, delivering a surprise of +0.57%.

Over the last four quarters, the company has beaten consensus EPS estimates two times.

Bottom LineAn earnings beat or miss may not be the sole basis for a stock moving higher or lower. Many stocks end up losing ground despite an earnings beat due to other factors that disappoint investors. Similarly, unforeseen catalysts help a number of stocks gain despite an earnings miss.

That said, betting on stocks that are expected to beat earnings expectations does increase the odds of success. This is why it's worth checking a company's Earnings ESP and Zacks Rank ahead of its quarterly release. Make sure to utilize our Earnings ESP Filter to uncover the best stocks to buy or sell before they've reported.

Equitable Holdings doesn't appear a compelling earnings-beat candidate. However, investors should pay attention to other factors too for betting on this stock or staying away from it ahead of its earnings release.

Expected Results of an Industry PlayerAmerican International Group (AIG - Free Report) , another stock in the Zacks Insurance - Multi line industry, is expected to report earnings per share of $1.9 for the quarter ended March 2026. This estimate points to a year-over-year change of +62.4%. Revenues for the quarter are expected to be $6.89 billion, up 4.1% from the year-ago quarter.

The consensus EPS estimate for American International Group has been revised 0.4% lower over the last 30 days to the current level. However, a higher Most Accurate Estimate has resulted in an Earnings ESP of +0.53%.

When combined with a Zacks Rank of #3 (Hold), this Earnings ESP indicates that American International Group will most likely beat the consensus EPS estimate. The company beat consensus EPS estimates in each of the trailing four quarters.

Stay on top of upcoming earnings announcements with the Zacks Earnings Calendar.
2026-06-12 16:37 1mo ago
2026-04-28 11:01 3mo ago
Assurant (AIZ) Reports Next Week: Wall Street Expects Earnings Growth
EQH Axa Equitable Holdings
FMP Stock News
Original source text
The market expects Assurant (AIZ - Free Report) to deliver a year-over-year increase in earnings on higher revenues when it reports results for the quarter ended March 2026. This widely-known consensus outlook is important in assessing the company's earnings picture, but a powerful factor that might influence its near-term stock price is how the actual results compare to these estimates.

The earnings report, which is expected to be released on May 5, might help the stock move higher if these key numbers are better than expectations. On the other hand, if they miss, the stock may move lower.

While management's discussion of business conditions on the earnings call will mostly determine the sustainability of the immediate price change and future earnings expectations, it's worth having a handicapping insight into the odds of a positive EPS surprise.

Zacks Consensus EstimateThis insurer is expected to post quarterly earnings of $5.40 per share in its upcoming report, which represents a year-over-year change of +59.3%.

Revenues are expected to be $3.3 billion, up 6.6% from the year-ago quarter.

Estimate Revisions TrendThe consensus EPS estimate for the quarter has been revised 1.42% lower over the last 30 days to the current level. This is essentially a reflection of how the covering analysts have collectively reassessed their initial estimates over this period.

Investors should keep in mind that the direction of estimate revisions by each of the covering analysts may not always get reflected in the aggregate change.

Price, Consensus and EPS Surprise

Earnings WhisperEstimate revisions ahead of a company's earnings release offer clues to the business conditions for the period whose results are coming out. This insight is at the core of our proprietary surprise prediction model -- the Zacks Earnings ESP (Expected Surprise Prediction).

The Zacks Earnings ESP compares the Most Accurate Estimate to the Zacks Consensus Estimate for the quarter; the Most Accurate Estimate is a more recent version of the Zacks Consensus EPS estimate. The idea here is that analysts revising their estimates right before an earnings release have the latest information, which could potentially be more accurate than what they and others contributing to the consensus had predicted earlier.

Thus, a positive or negative Earnings ESP reading theoretically indicates the likely deviation of the actual earnings from the consensus estimate. However, the model's predictive power is significant for positive ESP readings only.

A positive Earnings ESP is a strong predictor of an earnings beat, particularly when combined with a Zacks Rank #1 (Strong Buy), 2 (Buy) or 3 (Hold). Our research shows that stocks with this combination produce a positive surprise nearly 70% of the time, and a solid Zacks Rank actually increases the predictive power of Earnings ESP.

Please note that a negative Earnings ESP reading is not indicative of an earnings miss. Our research shows that it is difficult to predict an earnings beat with any degree of confidence for stocks with negative Earnings ESP readings and/or Zacks Rank of 4 (Sell) or 5 (Strong Sell).

How Have the Numbers Shaped Up for Assurant?For Assurant, the Most Accurate Estimate is higher than the Zacks Consensus Estimate, suggesting that analysts have recently become bullish on the company's earnings prospects. This has resulted in an Earnings ESP of +3.01%.

On the other hand, the stock currently carries a Zacks Rank of #3.

So, this combination indicates that Assurant will most likely beat the consensus EPS estimate.

Does Earnings Surprise History Hold Any Clue?Analysts often consider to what extent a company has been able to match consensus estimates in the past while calculating their estimates for its future earnings. So, it's worth taking a look at the surprise history for gauging its influence on the upcoming number.

For the last reported quarter, it was expected that Assurant would post earnings of $5.55 per share when it actually produced earnings of $5.61, delivering a surprise of +1.08%.

Over the last four quarters, the company has beaten consensus EPS estimates four times.

Bottom LineAn earnings beat or miss may not be the sole basis for a stock moving higher or lower. Many stocks end up losing ground despite an earnings beat due to other factors that disappoint investors. Similarly, unforeseen catalysts help a number of stocks gain despite an earnings miss.

That said, betting on stocks that are expected to beat earnings expectations does increase the odds of success. This is why it's worth checking a company's Earnings ESP and Zacks Rank ahead of its quarterly release. Make sure to utilize our Earnings ESP Filter to uncover the best stocks to buy or sell before they've reported.

Assurant appears a compelling earnings-beat candidate. However, investors should pay attention to other factors too for betting on this stock or staying away from it ahead of its earnings release.

Expected Results of an Industry PlayerAnother stock from the Zacks Insurance - Multi line industry, Equitable Holdings, Inc. (EQH - Free Report) , is soon expected to post earnings of $1.63 per share for the quarter ended March 2026. This estimate indicates a year-over-year change of +20.7%. Revenues for the quarter are expected to be $4.01 billion, up 5.9% from the year-ago quarter.

The consensus EPS estimate for Equitable Holdings has been revised 3.7% lower over the last 30 days to the current level. However, a lower Most Accurate Estimate has resulted in an Earnings ESP of -1.21%.

This Earnings ESP, combined with its Zacks Rank #4 (Sell), makes it difficult to conclusively predict that Equitable Holdings will beat the consensus EPS estimate. Over the last four quarters, the company surpassed consensus EPS estimates two times.

Stay on top of upcoming earnings announcements with the Zacks Earnings Calendar.
2026-06-12 16:37 1mo ago
2026-05-04 16:15 2mo ago
Equitable Holdings Reports First Quarter 2026 Results
EQH Axa Equitable Holdings
FMP Stock News
Original source text
NEW YORK--(BUSINESS WIRE)--Equitable Holdings, Inc. (“Equitable Holdings”, “Holdings”, or the “Company”) (NYSE: EQH) today announced financial results for the first quarter ended March 31, 2026.

“We reported solid first quarter results with Non-GAAP operating earnings per share of $1.62, or $1.68 excluding notable items, up 25% from the prior year quarter. Within our businesses, we continued to see healthy organic growth momentum, highlighted by $1.3 billion of net inflows in Retirement and $2.0 billion of advisory net inflows in Wealth Management. Looking forward, we remain confident in achieving our 2026 guidance of $1.8 billion of cash generation and over 15% growth in earnings per share,” said Mark Pearson, President and Chief Executive Officer.

Mr. Pearson concluded, “I am incredibly excited about the announced merger with Corebridge, which will create a diversified financial services company with leading positions across retirement, life insurance, asset management, and wealth management and accelerate our growth strategy. The transaction will be immediately accretive to earnings per share and cash generation, and we project at least 10% accretion on a run-rate basis by year-end 2028. By leveraging the complementary strengths of Equitable and Corebridge, the combined company will have the scale, product breadth, and distribution platform to deliver superior value to both our customers and shareholders.”

Consolidated Results

First Quarter

(in millions, except per share amounts or unless otherwise noted)

2026

2025

Total Assets Under Management/Administration (“AUM/A”, in billions)

$

1,094

$

1,006

Net income (loss) attributable to Holdings

621

63

Net income (loss) attributable to Holdings per common share

2.14

0.16

Non-GAAP operating earnings

472

421

Non-GAAP operating earnings per common share (“EPS”)

1.62

1.30

As of March 31, 2026, total AUM/A was $1.1 trillion, a year-over-year increase of 9%, driven by positive net flows and higher markets over the prior twelve months.

Net income (loss) attributable to Holdings for the first quarter of 2026 was $621 million compared to $63 million in the first quarter of 2025.

Non-GAAP operating earnings in the first quarter of 2026 were $472 million compared to $421 million in the first quarter of 2025. Adjusting for notable items3 of $19 million, first quarter 2026 Non-GAAP operating earnings were $491 million or $1.68 per share.

As of March 31, 2026, book value per common share including accumulated other comprehensive income (“AOCI”) was $(2.83). Book value per common share excluding AOCI was $19.56. Both of these measures reflect the Company’s 68% ownership stake in AllianceBernstein (“AB”) at book value. Book value per common share excluding AOCI but with AB reflected at fair market value was $34.70.

Business Highlights

First quarter 2026 business segment highlights: Retirement reported net inflows of $1.3 billion and first year premiums of $6.0 billion were up 10% over the prior year. Asset Management (AllianceBernstein or “AB”)4 reported net outflows of $7.1 billion, primarily driven by active equities. The institutional pipeline increased to a record $27.5 billion as of quarter end. Wealth Management (“WM”) reported advisory net inflows of $2.0 billion, with total assets under administration reaching $131 billion. Capital management program: The Company returned $223 million to shareholders in the first quarter, including $76 million quarterly cash dividends and $147 million of share repurchases. The Company remains committed to its 60-70% payout ratio target for 2026. The Company reported cash and liquid assets of $1.2 billion at Holdings5 as of quarter end, which remains above the $500 million minimum target. The combined NAIC RBC ratio was approximately 475% at year end, above the Company’s target of 400%. Delivering shareholder value: The Company has completed the deployment of its $20 billion capital committed to AB. This supports growth in AB’s Private Markets business, which had $85 billion of assets under management as of quarter end. During the first quarter, the Company closed on the acquisition of Stifel Independent Advisors, adding over $9 billion of client assets. On March 26th, the Company announced an agreement to combine with Corebridge Financial in an all-stock merger, creating an industry-leading Retirement, Wealth and Asset Management company. The merger is expected to close by year-end 2026, subject to a shareholder vote and regulatory approvals. The transaction is expected to be immediately accretive to earnings per share and cash generation with 10%+ accretion on a run rate basis by year-end 2028. Business Segment Results

Retirement

(in millions, unless otherwise noted)

Q1 2026

Q1 2025

Total Assets (in billions)6

$

175.7

$

154.6

Segment net flows (in billions)

1.3

1.6

Operating earnings (loss)

396

380

Assets increased by 14%, driven by market performance and net inflows over the prior twelve months. First year premiums of $6.0 billion increased by 10% while net inflows of $1.3 billion were lower than the prior year quarter. Operating earnings of $396 million increased versus the prior year quarter, primarily due to higher fee-based revenue and a lower tax rate. Operating earnings adjusted for notable items7 increased from $385 million in the prior year quarter to $394 million. Notable items of $(2) million in the current period reflect lower net investment income from alternatives, offset by a favorable tax credit. Asset Management

(in millions, unless otherwise noted)

Q1 2026

Q1 2025

Total AUM (in billions)

$

838.6

$

784.5

Segment net flows (in billions)

(7.1

)

2.4

Operating earnings (loss)

140

126

AUM increased by 7% due to market performance over the prior twelve months. Net outflows were $7.1 billion in the quarter, including net outflows of $5.8 billion in Retail and $1.9 billion in Institutional, partially offset by net inflows of $0.6 billion in Private Wealth. Operating earnings increased from $126 million in the prior year quarter to $140 million, due to growth in base fees and a higher ownership percentage of AB. Wealth Management

(in millions, unless otherwise noted)

Q1 2026

Q1 2025

Total AUA (in billions)

$

131.0

$

102.1

Advisory net new assets (in billions)

2.0

2.0

Operating earnings (loss)

55

45

AUA increased by 28% over the last twelve months due to market performance, net inflows and acquired assets from the Stifel transaction. Advisory net inflows were $2.0 billion in the quarter, supported by an 11% year-over-year increase in advisor productivity. Operating earnings increased from $45 million in the prior year quarter to $55 million, primarily due to growth in client assets and advisory fees. Corporate and Other (“C&O”)

The operating loss of $119 million in the first quarter decreased from an operating loss of $130 million in the prior year quarter. After adjusting for notable items8, the operating loss was $98 million versus a loss of $122 million in the prior year quarter.

____________________________

1 This press release includes certain Non-GAAP financial measures. More information on these measures and reconciliations to the most comparable U.S. GAAP measures can be found in the “Use of Non-GAAP Financial Measures” section of this release.

2 Please refer to Exhibit 1 for a detailed reconciliation and definitions related to notable items.

3

Please refer to Exhibit 1 for detailed reconciliation and definitions related to notable items.

4

Refers to AllianceBernstein L.P. and AllianceBernstein Holding L.P., collectively.

5

Excludes c. $195 million of cash at Holdings which is available to AllianceBernstein through its credit facility with Equitable Holdings.

6

Retirement assets includes account value (net of embedded derivatives), spread lending balances and reserves (excluding MRBs)

7

Please refer to Exhibit 1 for a detailed reconciliation and definitions related to notable items.

8

Please refer to Exhibit 1 for a detailed reconciliation and definitions related to notable items.

Exhibit 1: Notable Items

Notable items represent the impact on results from our annual actuarial assumption review, approximate impacts attributable to significant variances from the Company’s expectations, and other items that the Company believes may not be indicative of future performance. The Company chooses to highlight the impact of these items and give Non-GAAP measures less notable items to provide a better understanding of our results of operations in a given period. Certain figures may not sum due to rounding.

Impact of notable items by segment and Corporate & Other:

Three Months Ended March 31,

(in millions)

2026

2025

Non-GAAP Operating Earnings

$

472

$

421

Post-tax adjustments related to notable items:

Retirement

(2

)

5

Asset Management





Wealth Management





Corporate & Other

21

8

Non-GAAP Operating Earnings, less Notable Items

$

491

$

434

Impact of notable items by item category:

Three Months Ended March 31,

(in millions)

2026

2025

Non-GAAP Operating Earnings

$

472

$

421

Post-tax adjustments related to notable Items:

Net investment income

32

13

Tax credit

(13

)



Non-GAAP Operating Earnings, less Notable Items

$

491

$

434

Earnings Conference Call

Equitable Holdings will host a conference call at 9 a.m. ET on May 5, 2026 to discuss its first quarter 2026 results. The conference call webcast, along with additional earnings materials, will be accessible on the company’s investor relations website at ir.equitableholdings.com. Please log on to the webcast at least 15 minutes prior to the call to download and install any necessary software.

To register for the conference call, please use the following link:
EQH First Quarter 2026 Earnings Call

After registering, you will receive an email confirmation including dial in details and a unique conference call code for entry. Registration is open through the live call. To ensure you are connected for the full call we suggest registering a day in advance or at minimum 10 minutes before the start of the call.

A webcast replay will be made available on the Equitable Holdings Investor Relations website at ir.equitableholdings.com.

About Equitable Holdings

Equitable Holdings, Inc. (NYSE: EQH) is a leading financial services holding company comprised of complementary and well-established businesses, Equitable, AllianceBernstein and Equitable Advisors. Equitable Holdings has $1.1 trillion in assets under management and administration (as of 3/31/2026) and more than 5 million client relationships globally. Founded in 1859, Equitable provides retirement and protection strategies to individuals, families and small businesses. AllianceBernstein is a global investment management firm that offers diversified investment services to institutional investors, individuals and private wealth clients. Equitable Advisors, LLC (Equitable Financial Advisors in MI and TN) has approximately 4,600 duly registered and licensed financial professionals that provide financial planning, wealth management, retirement planning, protection and risk management services to clients across the country.

Note Regarding Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Words such as “expects,” “believes,” “anticipates,” “forecasts,” “intends,” “seeks,” “aims,” “plans,” “assumes,” “estimates,” “projects,” “should,” “would,” “could,” “may,” “will,” “shall” or variations of such words are generally part of forward-looking statements. Forward-looking statements are made based on management’s current expectations and beliefs concerning future developments and their potential effects upon Equitable Holdings, Inc. (“Holdings”) and its consolidated subsidiaries. These forward-looking statements include, but are not limited to, statements regarding projections, estimates, forecasts and other financial and performance metrics and projections of market expectations. “We,” “us” and “our” refer to Holdings and its consolidated subsidiaries, unless the context refers only to Holdings as a corporate entity. There can be no assurance that future developments affecting Holdings will be those anticipated by management. Forward-looking statements include, without limitation, all matters that are not historical facts.

These forward-looking statements are not a guarantee of future performance and involve risks and uncertainties, and there are certain important factors that could cause actual results to differ, possibly materially, from expectations or estimates reflected in such forward-looking statements, including, among others: (i) the ability to complete the Proposed Transaction on the timeframe or in the terms currently anticipated or at all, including due to a failure to obtain requisite stockholder, stock exchange, regulatory, governmental or other approvals; (ii) risks related to difficulties, inabilities or delays in integrating the parties’ businesses; (iii) the ability to realize the anticipated benefits of the Proposed Transaction, including estimated run-rate expense synergies and projected cost savings at the time, and to the extent anticipated, as well as expected, operating earnings and cash flow generation; (iv) the occurrence of any event, change or other circumstance that could give rise to the right of either or both parties to terminate the merger agreement; (v) the potential impact of the announcement or consummation of the Proposed Transaction on Equitable or Corebridge’s stock price and on their respective business, contractual and operational relationships (including with regulatory bodies, employees, suppliers, clients and competitors); (vi) risk related to business disruptions from the Proposed Transaction that may harm the business or current plans and operations of either or both parties, including diversion of management time from ongoing business operations; (vii) the risk that the Proposed Transaction and the announcement thereof could have an adverse effect on the operations; (viii) the risk that the Proposed Transaction and the announcement thereof could have an adverse effect on the ability of either or both parties to hire and retain key personnel; (ix) the parties’ ability to raise debt on favorable terms or at all; (x) the outcome of any legal proceedings that may be instituted against Equitable, Corebridge, their new parent company or their respective directors; (xi) restrictions on the conduct of Equitable and Corebridge’s respective businesses prior to the closing of the Proposed Transaction and on each of their ability to pursue alternatives to the Proposed Transaction; (xii) the possibility that the Proposed Transaction may be more expensive to complete than anticipated, including as a result of unexpected factors or events, or unforeseen or unknown liabilities; (xiii) the potential impact of a downgrade in Equitable or Corebridge’s Insurer Financial Strength ratings or credit ratings or of the new parent company of Equitable and Corebridge following completion of the Proposed Transaction; (xiv) conditions in the financial markets and economy, including the impact of geopolitical conflicts, changes in tariffs and trade barriers, the impact on the Company of a continued shutdown of the U.S. government, and related economic conditions, equity market declines and volatility, interest rate fluctuations, impacts on our goodwill and changes in liquidity and access to and cost of capital; (xv) operational factors, including reliance on the payment of dividends to Holdings by its subsidiaries, protection of confidential customer information or proprietary business information, operational failures by us or our service providers, potential strategic transactions, changes in accounting standards, and catastrophic events, such as the outbreak of pandemic diseases; (xvi) credit, counterparties and investments, including counterparty default on derivative contracts, failure of financial institutions, defaults by third parties and affiliates and economic downturns, defaults and other events adversely affecting our investments; (xvii) our reinsurance and hedging programs; (xviii) our products, structure and product distribution, including variable annuity guaranteed benefits features within certain of our products, variations in statutory capital requirements, financial strength and claims-paying ratings, state insurance laws limiting the ability of our insurance subsidiaries to pay dividends and key product distribution relationships; (xix) estimates, assumptions and valuations, including risk management policies and procedures, potential inadequacy of reserves and experience differing from pricing expectations, amortization of deferred acquisition costs and financial models; (xx) our Asset Management segment, including fluctuations in assets under management and the industry-wide shift from actively-managed investment services to passive services; (xxi) recruitment and retention of key employees and experienced and productive financial professionals; (xxii) subjectivity of the determination of the amount of allowances and impairments taken on our investments; (xxiii) legal and regulatory risks, including federal and state legislation affecting financial institutions, insurance regulation and tax reform; (xxiv) risks related to our common stock and (xxv) general risks, including strong industry competition, information systems failing or being compromised and protecting our intellectual property.

Forward-looking statements, including any financial guidance, should be read in conjunction with the other cautionary statements, risks, uncertainties and other factors identified in Holdings’ filings with the Securities and Exchange Commission. Further, any forward-looking statement speaks only as of the date on which it is made, and we undertake no obligation to update or revise any forward-looking statement to reflect events or circumstances after the date on which the statement is made or to reflect the occurrence of unanticipated events, except as otherwise may be required by law.

Forward-looking Non-GAAP Metrics

The Company has presented forward-looking statements regarding Non-GAAP operating earnings, and Non-GAAP operating earnings per share. These non-GAAP financial measures are derived by excluding certain amounts, expenses or income, from the corresponding financial measures determined in accordance with GAAP. The determination of the amounts that are excluded from these non-GAAP financial measures is a matter of management judgment and depends upon, among other factors, the nature of the underlying expense or income amounts recognized in a given period. We are unable to present a quantitative reconciliation of forward-looking adjusted operating earnings per share and payout ratio targeted to non-GAAP operating earnings to their most directly comparable forward-looking GAAP financial measures because such information is not available, and management cannot reliably predict all of the necessary components of such GAAP measures without unreasonable effort or expense. In addition, we believe such reconciliations would imply a degree of precision that would be confusing or misleading to investors. The unavailable information could have a significant impact on the Company’s future financial results. These non-GAAP financial measures are preliminary estimates and are subject to risks and uncertainties, including, among others changes in connection with quarter-end and year-end adjustments. Any variations between the Company’s actual results and preliminary financial data set forth above may be material.

Use of Non-GAAP Financial Measures

In addition to our results presented in accordance with U.S. GAAP, we report Non-GAAP Operating Earnings, and Non-GAAP operating common EPS, each of which is a measure that is not determined in accordance with U.S. GAAP. Management principally uses these Non-GAAP financial measures in evaluating performance because they present a clearer picture of our operating performance and they allow management to allocate resources. Similarly, management believes that the use of these Non-GAAP financial measures, together with relevant U.S. GAAP measures, provide investors with a better understanding of our results of operations and the underlying profitability drivers and trends of our business. These Non-GAAP financial measures are intended to remove from our results of operations the impact of market changes (where there is a mismatch in the valuation of assets and liabilities) as well as certain other expenses which are not part of our underlying profitability drivers or likely to re-occur in the foreseeable future, as such items fluctuate from period-to-period in a manner inconsistent with these drivers. These measures should be considered supplementary to our results that are presented in accordance with U.S. GAAP and should not be viewed as a substitute for the U.S. GAAP measures. Other companies may use similarly titled Non-GAAP financial measures that are calculated differently from the way we calculate such measures. Consequently, our Non-GAAP financial measures may not be comparable to similar measures used by other companies.

We also discuss certain operating measures, including AUM, AUA, AV, policy reserves and certain other operating measures, which management believes provide useful information about our businesses and the operational factors underlying our financial performance.

Non-GAAP Operating Earnings

Non-GAAP Operating Earnings is an after-tax Non-GAAP financial measure used to evaluate our financial performance on a consolidated basis that is determined by making certain adjustments to our consolidated after-tax net income attributable to Holdings. The most significant of such adjustments relates to our derivative positions, which protect economic value and statutory capital, and the variable annuity product MRBs. This is a large source of volatility in net income.

Non-GAAP Operating Earnings equals our consolidated after-tax net income attributable to Holdings adjusted to eliminate the impact of the following items:

Items related to variable annuity product features, which include: (i) changes in the fair value of MRB and purchased MRB, including the related attributed fees and claims, offset by derivatives and other securities used to hedge the MRB which result in residual net income volatility as the change in fair value of certain securities is reflected in OCI and due to our statutory capital hedge program; and (ii) market adjustments to deposit asset or liability accounts arising from reinsurance agreements which do not expose the reinsurer to a reasonable possibility of a significant loss from insurance risk; Investment (gains) losses, which includes credit loss impairments of securities/investments, sales or disposals of securities/investments, realized capital gains/losses and valuation allowances; Net actuarial (gains) losses, which includes actuarial gains and losses as a result of differences between actual and expected experience on pension plan assets or projected benefit obligation during a given period related to pension, other postretirement benefit obligations, and the one-time impact of the settlement of the defined benefit obligation; Other adjustments, which primarily include restructuring costs related to severance and separation, lease write-offs related to non-recurring restructuring activities, net derivative gains (losses) on certain Non-GMxB derivatives, net investment income from certain items including consolidated VIE investments, seed capital mark-to-market adjustments, unrealized gain/losses and realized capital gains/losses from sales or disposals of select securities, certain legal accruals; a bespoke deal to repurchase UL policies from one entity that had invested in numerous policies purchased in the life settlement market, which disposed of the risk of additional COI litigation by that entity related to those UL policies, impact of the annual actuarial assumption updates attributable to LFPB when the majority of the impact relates to the non-core business; and Income tax expense (benefit) related to the above items and non-recurring tax items, which includes the effect of uncertain tax positions for a given audit period and changes to the deferred tax valuation allowance. In the third quarter of 2025, the Company updated its net investment income (“NII”) segment reporting to better align with our GAAP segments, as well as the reporting of our spread lending programs' income and expenses. Previously, direct and allocated segment NII were recorded based on assets tied to statutory asset tagging and net statutory liabilities for allocation. To better align with our GAAP segments, the Company changed the recording methodology for direct NII. It is now based on the book yields of assets tied to specific segments, considering general account values plus reserves, net of embedded derivatives. Indirect NII, which was previously allocated based on net statutory liabilities, is now allocated based on general account values and reserves, net of embedded derivatives. Additionally, revenues and expenses from our spread lending programs are now primarily recorded within the Retirement segment. Previously, spread lending revenues and expenses were recorded in Corporate and Other, with the excess of revenues over expenses allocated to the insurance segments based on net statutory liabilities. Prior periods have been revised to reflect these changes.

Because Non-GAAP Operating Earnings excludes the foregoing items that can be distortive or unpredictable, management believes that this measure enhances the understanding of the Company’s underlying drivers of profitability and trends in our business, thereby allowing management to make decisions that will positively impact our business.

We use the prevailing corporate federal income tax rate of 21% while taking into account any non-recurring differences for events recognized differently in our financial statements and federal income tax returns as well as partnership income taxed at lower rates when reconciling Net income (loss) attributable to Holdings to Non-GAAP Operating Earnings.

The table below presents a reconciliation of Net income (loss) attributable to Holdings to Non-GAAP Operating Earnings for the three months ended March 31, 2026 and 2025:

Three Months Ended March 31,

(in millions)

2026

2025

Net income (loss) attributable to Holdings

$

621

$

63

Adjustments related to:

Variable annuity product features (1)

(386

)

211

Investment (gains) losses

29

14

Net actuarial (gains) losses related to pension and other postretirement benefit obligations

14

11

Other adjustments (2)

148

205

  Income tax expense (benefit) related to above adjustments

41

(92

)

Non-recurring tax items

5

9

Non-GAAP Operating Earnings

$

472

$

421

Non-GAAP Operating EPS

Non-GAAP Operating Earnings per common share is calculated by dividing Non-GAAP Operating Earnings less preferred stock dividends by diluted common shares outstanding. The table below presents a reconciliation of GAAP EPS to Non-GAAP Operating EPS for the three months ended March 31, 2026 and 2025.

Three Months Ended March 31,

(per share amounts)

2026

2025

Net income (loss) attributable to Holdings

$

2.19

$

0.20

Less: Preferred stock dividend

0.05

0.04

Net Income (loss) available to common shareholders

2.14

0.16

Adjustments related to:

Variable annuity product features (1)

(1.36

)

0.68

Investment (gains) losses

0.10

0.04

Net actuarial (gains) losses related to pension and other postretirement benefit obligations

0.05

0.04

Other adjustments (2)

0.53

0.64

  Income tax expense (benefit) related to above adjustments

0.14

(0.29

)

Non-recurring tax items

0.02

0.03

Non-GAAP Operating Earnings

$

1.62

$

1.30

Book Value per common share, excluding AOCI

We use the term “book value” to refer to total equity attributable to Holdings’ common shareholders. Book Value per common share, excluding AOCI, is our total equity attributable to Holdings, excluding AOCI and preferred stock, divided by ending common shares outstanding.

March 31,
2026

December 31,
2025

Book value per common share

$

(2.83

)

$

(4.03

)

Per share impact of AOCI

22.39

22.17

Book Value per common share, excluding AOCI

$

19.56

$

18.14

Other Operating Measures

We also use certain operating measures which management believes provide useful information about our businesses and the operational factors underlying our financial performance.

Account Value (“AV”)

Account value generally equals the aggregate policy account value of our retirement products.

Assets Under Management (“AUM”)

AUM means investment assets that are managed by one of our subsidiaries and includes: (i) assets managed by AB, (ii) the assets in our general account investment portfolio and (iii) the separate account assets of our Retirement and Life businesses. Total AUM reflects exclusions between segments to avoid double counting.

Assets Under Management (“AUA”)

AUA means advisory and brokerage investment assets included in the Company’s Wealth Management segment.

Segment net flows

Net change in segment customer account balances in a period including, but not limited to, gross premiums, surrenders, withdrawals and benefits. It excludes investment performance, interest credited to customer accounts and policy charges.

Consolidated Statements of Income (Loss) (Unaudited)

Three Months Ended March 31,

2026

2025

(in millions)

REVENUES

Policy charges and fee income

$

429

$

636

Premiums

240

304

Net derivative gains (losses)

580

799

Net investment income (loss)

1,284

1,248

Investment gains (losses), net:

Credit and intent to sell losses on available-for-sale debt securities and loans

7



Other investment gains (losses), net

(36

)

(14

)

Total investment gains (losses), net

(29

)

(14

)

Investment management and service fees

1,327

1,285

Other income

399

318

Total revenues

4,230

4,576

BENEFITS AND OTHER DEDUCTIONS

Policyholders’ benefits

385

759

Remeasurement of liability for future policy benefits

9

(2

)

Change in market risk benefits and purchased market risk benefits

325

672

Interest credited to policyholders’ account balances

770

678

Compensation and benefits

625

601

Commissions and distribution-related payments

556

501

Interest expense

62

55

Amortization of deferred policy acquisition costs

209

188

Other operating costs and expenses

402

950

Total benefits and other deductions

3,343

4,402

Income (loss) from continuing operations, before income taxes

887

174

Income tax (expense) benefit

(156

)

(24

)

Net income (loss)

731

150

Less: Net income (loss) attributable to the noncontrolling interest

110

87

Net income (loss) attributable to Holdings

621

63

Less: Preferred stock dividends

14

14

Net income (loss) available to Holdings’ common shareholders

$

607

$

49

Earnings Per Common Share

Three Months Ended March 31,

2026

2025

(in millions)

Earnings per common share

Basic

$

2.16

$

0.16

Diluted

$

2.14

$

0.16

Weighted average shares

Weighted average common stock outstanding for basic earnings per common share

281.3

307.8

Weighted average common stock outstanding for diluted earnings per common share

283.8

311.9

Results of Operations by Segment

Three Months Ended March 31,

2026

2025

(in millions)

Operating earnings (loss) by segment:

Retirement

$

396

$

380

Asset Management

140

126

Wealth Management

55

45

Corporate and Other

(119

)

(130

)

Non-GAAP Operating Earnings

$

472

$

421

Select Balance Sheet Statistics

March 31,
2026

December 31,
2025

(in millions)

ASSETS

Total investments and cash and cash equivalents

$

131,583

$

133,466

Separate Accounts assets

130,470

136,544

Total assets

$

310,382

$

317,990

LIABILITIES

Long-term debt

$

3,837

$

3,835

Future policy benefits and other policyholders' liabilities

17,441

17,660

Policyholders’ account balances

132,662

133,433

Total liabilities

$

308,132

$

316,202

EQUITY

Preferred stock

$

1,068

$

1,068

Accumulated other comprehensive income (loss)

(6,300

)

(6,280

)

Total equity attributable to Holdings

273

(74

)

Total equity attributable to Holdings' common shareholders (ex. AOCI)

5,505

5,138

Assets Under Management (Unaudited)

March 31,
2026

December 31,
2025

(in billions)

Assets Under Management

AB AUM

$

838.6

$

866.9

Exclusion for General Account and other Affiliated Accounts

(88.8

)

(87.3

)

Exclusion for Separate Accounts

(48.8

)

(51.0

)

AB third party

$

701.0

$

728.6

Total Company AUM

AB third party

$

701.0

$

728.6

General Account and other Affiliated Accounts (1) (3) (4) (5)

131.6

133.5

Separate Accounts (2) (3) (4) (5)

130.5

136.5

Total AUM

$

963.1

$

998.6

_______________ (1)

“General Account and other Affiliated Accounts” refers to assets held in the general accounts of our insurance companies and other assets on which we bear the investment risk.

(2)

“Separate Accounts” refers to the separate account investment assets of our insurance subsidiaries excluding any assets on which we bear the investment risk.

(3)

As of March 31, 2026 and December 31, 2025, Separate Accounts AUM is inclusive of $7.6 billion and $8.2 billion & General Account AUM is inclusive of $27 million and $28 million, respectively, ceded to Venerable.

(4)

As of March 31, 2026 and December 31, 2025, Separate Accounts AUM is inclusive of $6.8 billion and $7.2 billion & General Account AUM is inclusive of $2.9 billion and $3.0 billion, respectively, ceded to Global Atlantic.

(5)

Includes Advisory, Brokerage and Direct assets included in our Wealth Management segment.

As of March 31, 2026 and December 31, 2025, Separate Accounts AUM is inclusive of $14.5 billion and $15.1 billion & General Account AUM is inclusive of $9.3 billion and $9.3 billion, respectively, ceded to RGA. More News From Equitable Holdings, Inc.
2026-06-12 16:37 1mo ago
2026-05-04 20:30 2mo ago
Equitable Holdings, Inc. (EQH) Q1 Earnings Surpass Estimates
EQH Axa Equitable Holdings
FMP Stock News
Original source text
Equitable Holdings, Inc. (EQH - Free Report) came out with quarterly earnings of $1.62 per share, beating the Zacks Consensus Estimate of $1.6 per share. This compares to earnings of $1.35 per share a year ago. These figures are adjusted for non-recurring items.

This quarterly report represents an earnings surprise of +1.27%. A quarter ago, it was expected that this company would post earnings of $1.75 per share when it actually produced earnings of $1.76, delivering a surprise of +0.57%.

Over the last four quarters, the company has surpassed consensus EPS estimates two times.

Equitable Holdings, which belongs to the Zacks Insurance - Multi line industry, posted revenues of $3.61 billion for the quarter ended March 2026, missing the Zacks Consensus Estimate by 7.31%. This compares to year-ago revenues of $3.78 billion. The company has not been able to beat consensus revenue estimates over the last four quarters.

The sustainability of the stock's immediate price movement based on the recently-released numbers and future earnings expectations will mostly depend on management's commentary on the earnings call.

Equitable Holdings shares have lost about 11.5% since the beginning of the year versus the S&P 500's gain of 5.6%.

What's Next for Equitable Holdings?While Equitable Holdings has underperformed the market so far this year, the question that comes to investors' minds is: what's next for the stock?

There are no easy answers to this key question, but one reliable measure that can help investors address this is the company's earnings outlook. Not only does this include current consensus earnings expectations for the coming quarter(s), but also how these expectations have changed lately.

Empirical research shows a strong correlation between near-term stock movements and trends in earnings estimate revisions. Investors can track such revisions by themselves or rely on a tried-and-tested rating tool like the Zacks Rank, which has an impressive track record of harnessing the power of earnings estimate revisions.

Ahead of this earnings release, the estimate revisions trend for Equitable Holdings was unfavorable. While the magnitude and direction of estimate revisions could change following the company's just-released earnings report, the current status translates into a Zacks Rank #4 (Sell) for the stock. So, the shares are expected to underperform the market in the near future. You can see the complete list of today's Zacks #1 Rank (Strong Buy) stocks here.

It will be interesting to see how estimates for the coming quarters and the current fiscal year change in the days ahead. The current consensus EPS estimate is $1.77 on $3.95 billion in revenues for the coming quarter and $7.22 on $15.98 billion in revenues for the current fiscal year.

Investors should be mindful of the fact that the outlook for the industry can have a material impact on the performance of the stock as well. In terms of the Zacks Industry Rank, Insurance - Multi line is currently in the top 35% of the 250 plus Zacks industries. Our research shows that the top 50% of the Zacks-ranked industries outperform the bottom 50% by a factor of more than 2 to 1.

Kemper (KMPR - Free Report) , another stock in the same industry, has yet to report results for the quarter ended March 2026. The results are expected to be released on May 6.

This insurance holding company is expected to post quarterly earnings of $0.81 per share in its upcoming report, which represents a year-over-year change of -50.9%. The consensus EPS estimate for the quarter has remained unchanged over the last 30 days.

Kemper's revenues are expected to be $1.21 billion, up 1.9% from the year-ago quarter.
2026-06-12 16:37 1mo ago
2026-05-04 21:00 2mo ago
Equitable Holdings (EQH) Q1 Earnings: How Key Metrics Compare to Wall Street Estimates
EQH Axa Equitable Holdings
FMP Stock News
Original source text
Equitable Holdings, Inc. (EQH - Free Report) reported $3.61 billion in revenue for the quarter ended March 2026, representing a year-over-year decline of 4.5%. EPS of $1.62 for the same period compares to $1.35 a year ago.

The reported revenue compares to the Zacks Consensus Estimate of $3.9 billion, representing a surprise of -7.31%. The company delivered an EPS surprise of +1.27%, with the consensus EPS estimate being $1.60.

While investors scrutinize revenue and earnings changes year-over-year and how they compare with Wall Street expectations to determine their next move, some key metrics always offer a more accurate picture of a company's financial health.

As these metrics influence top- and bottom-line performance, comparing them to the year-ago numbers and what analysts estimated helps investors project a stock's price performance more accurately.

Here is how Equitable Holdings performed in the just reported quarter in terms of the metrics most widely monitored and projected by Wall Street analysts:

Retirement - Net flows: $1.29 billion compared to the $1.57 billion average estimate based on two analysts.Retirement - Total asset value end of period: $175.68 billion compared to the $176.53 billion average estimate based on two analysts.Wealth Management - Advisory net new assets: $2.02 billion versus $2.27 billion estimated by two analysts on average.Wealth Management - Total Wealth Management ending assets: $131.04 billion versus the two-analyst average estimate of $122.29 billion.Revenue- Policy charges, fee income and premiums: $669 million compared to the $674.25 million average estimate based on three analysts.Revenue- Investment management, service fees and other income: $1.68 billion compared to the $1.78 billion average estimate based on two analysts.Segment revenues- Corporate and Other: $525 million versus the two-analyst average estimate of $590.49 million. The reported number represents a year-over-year change of +157.4%.Revenue- Retirement- Policy charges, fee income and premiums: $307 million versus $324.87 million estimated by two analysts on average. Compared to the year-ago quarter, this number represents a +37.1% change.Revenue- Retirement- Net investment income (loss): $1.19 billion versus the two-analyst average estimate of $1.19 billion. The reported number represents a year-over-year change of +72.2%.Revenue- Retirement- Net derivative gains (losses): $-6 million versus the two-analyst average estimate of $-3.5 million. The reported number represents a year-over-year change of +20%.Revenue- Retirement- Investment management, service fees and other income: $185 million versus the two-analyst average estimate of $186.25 million. The reported number represents a year-over-year change of +117.7%.Revenue- Wealth Management- Net investment income (loss): $3 million compared to the $3.5 million average estimate based on two analysts. The reported number represents a change of 0% year over year.View all Key Company Metrics for Equitable Holdings here>>>

Shares of Equitable Holdings have returned +11.6% over the past month versus the Zacks S&P 500 composite's +10% change. The stock currently has a Zacks Rank #4 (Sell), indicating that it could underperform the broader market in the near term.
2026-06-12 16:37 1mo ago
2026-05-05 16:31 2mo ago
Equitable Holdings, Inc. (EQH) Q1 2026 Earnings Call Transcript
EQH Axa Equitable Holdings
FMP Stock News
Original source text
Equitable Holdings, Inc. (EQH) Q1 2026 Earnings Call Transcript
2026-06-12 16:37 1mo ago
2026-05-11 23:56 2mo ago
Is Equitable Holdings Inc (EQH) a Bargain After 3.8% Drop? GF Value Says Undervalued
EQH Axa Equitable Holdings
FMP Stock News
Original source text
On May 11, 2026, Equitable Holdings Inc (EQH) shares fell 3.8% today, currently priced at $40.99. The stock has traded within a 52-week range of $35.20 to $56.6
2026-06-12 16:37 1mo ago
2026-05-12 08:30 2mo ago
Corebridge Financial and Equitable Holdings Announce Leadership Team for Combined Company
EQH Axa Equitable Holdings
FMP Stock News
Original source text
HOUSTON & NEW YORK--(BUSINESS WIRE)--Corebridge Financial (NYSE: CRBG) (“Corebridge”) and Equitable Holdings, Inc. (NYSE: EQH) (“Equitable Holdings”) today announced the leadership team for the future combined company, effective upon completion of the previously announced merger.

“Together, the complementary offerings and capabilities of Corebridge and Equitable will enhance customer outcomes and drive long-term shareholder value. This will require a leadership team that is uniquely positioned to deliver on behalf of our stakeholders and lead the new company forward,” said Marc Costantini, President and Chief Executive Officer of Corebridge, who will serve as Chief Executive Officer of the combined company. “The exceptional talent and leadership we intend to bring together will enable us to move with speed, clarity and confidence once the transaction is complete.”

“When two organizations come together, our focus must go beyond combining capabilities to include the culture that will give those capabilities meaning and purpose,” said Mark Pearson, President and Chief Executive Officer of Equitable Holdings, who will serve as Executive Chair of the combined company. “Our leadership team understands this responsibility and is committed to creating a new culture that draws on the strengths of both organizations and keeps clients at the heart of every decision.”

Today, the company announced the following leaders will report to Chief Executive Officer Marc Costantini upon close:

As previously announced, Robin M. Raju will serve as Chief Financial Officer of the combined company, with responsibility for financial reporting, asset-liability management, strategic financial planning, M&A and investor relations, in addition to key capital management initiatives that drive growth and shareholder value. He will also oversee investment management for the combined company’s separate account funds. Mr. Raju is currently Chief Financial Officer for Equitable Holdings and has been with the company for more than two decades. Jeffrey J. Hurd will serve as Chief Operating Officer and Chief Human Resources Officer, overseeing client and advisor support and service operations, human resources, marketing, communications and corporate services for the combined company. He will also lead the joint Integration Office, ensuring a structured and consistent approach for integrating the two organizations post-close. Mr. Hurd currently serves as Chief Operating Officer for Equitable Holdings, a role he has held for nearly a decade, following a 20-year career with AIG. Polly Klane will serve as General Counsel and Chief Legal Officer, overseeing all legal, compliance, board governance, regulatory and governmental affairs for the combined company. Ms. Klane is currently General Counsel and Chief Legal Officer for Corebridge and previously served as General Counsel and Chief Legal Officer for Citizens Financial Group. Seth Bernstein will continue to serve as Chief Executive Officer of AllianceBernstein, the combined company’s global asset management business serving institutional, high-net-worth and retail investors. Onur Erzan, who was recently appointed President of AllianceBernstein and leads the firm’s Private Wealth Management, Global Asset Management Distribution and Global Private Alternatives businesses, will also join the combined company’s leadership team. John Byrne will lead Individual Distribution, overseeing the combined company’s wholesale distribution network for its annuity and life insurance products. This will include more than 900 relationships with banks, broker-dealers and independent marketing organizations. Mr. Byrne is currently President of Financial Distributors for Corebridge and has been with the company for more than two decades. David Karr will lead the combined company’s Wealth Management business, which will include Equitable Advisors and Corebridge financial professionals. Mr. Karr has been with the company for three decades and currently serves as Chair of Equitable Advisors, overseeing the growth strategy for Equitable Holdings’ fastest-growing business. Lisa Longino will serve as Chief Investment Officer, responsible for leading the investment strategy for the combined company’s c.$366 billion General Account. Ms. Longino currently serves as Chief Investment Officer for Corebridge, a role she has held since 2023. Prior to this, she was Head of Global Investment Strategy for Prudential Financial, after spending two decades at MetLife. Jonathan Novak will lead Institutional Markets for the combined company, which will serve public and corporate pension plans, endowments and foundations, insurers and other large financial institutions. Mr. Novak currently leads Institutional Markets, enterprise in-force management and reinsurance for Corebridge. He has been with the company for nearly 15 years. Bryan Pinsky will lead the Individual Retirement and Life Insurance businesses, which will include the combined company’s leading annuity and life insurance portfolios. Mr. Pinsky currently serves as Corebridge’s President of Individual Retirement and Life Insurance. He has been with the company for more than a decade, previously serving as President of Individual Retirement. Steve Scanlon will lead Group Retirement, overseeing the combined company’s workplace retirement offerings, which will include leading positions in the 403(b) and 457 markets, and its Employee Benefits business. Mr. Scanlon currently leads Equitable’s Individual Retirement business, previously led its Group Retirement business and has been with the company for more than 15 years, including a decade at AllianceBernstein. David Ditillo will serve as Chief Information Technology Officer, leading the combined company’s aspiration to enhance the customer experience through technology and digital solutions. Mr. Ditillo currently serves as Chief Information Officer for Corebridge, a role he has held since 2020, and also oversees resiliency and physical security for the company. Prior to this, he spent two decades at MetLife. Julia Zhang will serve as Chief Risk Officer, responsible for the combined company’s Enterprise Risk Management function to protect the new company’s balance sheet, while supporting growth. She will also have administrative oversight of the Audit function. Ms. Zhang is currently Chief Risk Officer for Equitable Holdings and has been with the company for nearly two decades, previously serving as Head of Treasury and Derivatives. On March 26, 2026, Corebridge Financial and Equitable Holdings announced the intention to combine in an all-stock merger to create a leading retirement, life, wealth and asset management company with more than 12 million customers and $1.5 trillion in assets under management and administration. The transaction is expected to close by year-end 2026, subject to shareholder and regulatory approvals and the satisfaction of other customary closing conditions.

About Corebridge Financial

Corebridge Financial, Inc. (NYSE: CRBG) makes it possible for more people to take action in their financial lives. With more than $380 billion in assets under management and administration as of March 31, 2026, Corebridge Financial is one of the largest providers of retirement solutions and insurance products in the United States. We proudly partner with financial professionals and institutions to help individuals plan, save for and achieve secure financial futures. For more information, visit corebridgefinancial.com and follow us on LinkedIn, YouTube and Instagram. These references with additional information about Corebridge have been provided as a convenience, and the information contained on such websites is not incorporated by reference into this press release.

About Equitable Holdings

Equitable Holdings, Inc. (NYSE: EQH) is a leading financial services holding company comprised of complementary and well-established businesses, Equitable, AllianceBernstein and Equitable Advisors. Equitable Holdings has $1.1 trillion in assets under management and administration (as of 3/31/2026) and more than 5 million client relationships globally. Founded in 1859, Equitable provides retirement and protection strategies to individuals, families and small businesses. AllianceBernstein is a global investment management firm that offers diversified investment services to institutional investors, individuals and private wealth clients. Equitable Advisors, LLC (Equitable Financial Advisors in MI and TN) has approximately 4,600 duly registered and licensed financial professionals that provide financial planning, wealth management, retirement planning, protection and risk management services to clients across the country.

Cautionary Statement Regarding Forward-Looking Information

This press release includes statements, which, to the extent they are not statements of historical or present fact, constitute “forward-looking statements” within the meaning of the U.S. Private Securities Litigation Reform Act of 1995. Forward-looking statements, and any related oral statements, can be identified by the use of terms such as “believes,” “expects,” “may,” “will,” “shall,” “should,” “would,” “could,” “seeks,” “aims,” “projects,” “forecasts,” “intends,” “targets,” “plans,” “estimates,” “anticipates,” “goals,” “guidance,” “formidable,” “preliminary,” “objective,” “continue,” “drive,” “improve,” “superior,” “robust,” “positioned,” “resilient,” “vision,” “potential,” “immediate,” and similar expressions or the negative of those expressions or verbs. We caution you that forward-looking statements are not guarantees of future performance or outcomes. Forward-looking statements are not historical facts but instead represent only our beliefs regarding future events, which may by their nature be inherently uncertain, and some of which may be outside our control. These statements include, but are not limited to, statements about the potential repurchases of shares of common stock, the expected timing and completion of the proposed transaction between Corebridge Financial, Inc. (“Corebridge”) and Equitable Holdings, Inc. (“Equitable Holdings”) (the “Proposed Transaction”), the anticipated benefits of the Proposed Transaction, including estimated synergies and projected cost savings, and plans and expectations for Corebridge, Equitable Holdings or their new parent company after completion of the Proposed Transaction.

Such forward-looking statements are subject to known and unknown risks, uncertainties, assumptions and other factors that may cause the actual results, level of activity, performance or achievements to be materially different from those expressed or implied by such forward-looking statements. Key factors include, among others, the ability to repurchase shares (if Corebridge and / or Equitable Holdings decide to do so) within the expected timing or at all; the ability to complete the Proposed Transaction on the timeframe or on the terms currently anticipated or at all, including due to a failure to obtain requisite stockholder, stock exchange, regulatory, governmental or other approvals; risks related to difficulties, inabilities or delays in integrating the parties’ businesses; the ability to realize the anticipated benefits of the Proposed Transaction, including estimated run-rate expense synergies and projected cost savings at the times, and to the extent, anticipated, as well as expected operating earnings and cashflow generation; the occurrence of any event, change or other circumstance that could give rise to the right of either or both parties to terminate the merger agreement; the potential impact of the announcement or consummation of the Proposed Transaction on Corebridge or Equitable Holdings’ stock price and on their respective business, contractual and operational relationships (including with regulatory bodies, employees, suppliers, clients and competitors); risks related to business disruptions from the Proposed Transaction that may harm the business or current plans and operations of either or both parties, including diversion of management time from ongoing business operations; the risk that the Proposed Transaction and its announcement could have an adverse effect on the ability of either or both parties to hire and retain key personnel; the parties’ ability to raise debt on favorable terms or at all; the outcome of any legal proceedings that may be instituted against Corebridge, Equitable Holdings, their new parent company or their respective directors; restrictions on the conduct of Corebridge and Equitable Holdings’ respective businesses prior to the closing of the Proposed Transaction and on each of their ability to pursue alternatives to the Proposed Transaction; the possibility that the Proposed Transaction may be more expensive to complete than anticipated, including as a result of unexpected factors or events, or unforeseen or unknown liabilities; the deterioration of economic conditions; geopolitical tensions; the potential impact of a downgrade in Corebridge or Equitable Holdings’ Insurer Financial Strength ratings or credit ratings or of the new parent company of Corebridge and Equitable Holdings following completion of the Proposed Transaction; other factors that may affect future results of Corebridge and Equitable Holdings; and management’s response to any of the aforementioned factors.

The foregoing list of factors is not exhaustive. You should carefully consider these factors and the other risks and uncertainties described in the “Risk Factors” section of the new parent company’s Registration Statement on Form S-4 and other documents filed or furnished by Corebridge and Equitable Holdings from time to time with the U.S. Securities and Exchange Commission (the “SEC”), including their Annual Reports on Form 10-K for the year ended December 31, 2025. These filings identify and address other important risks and uncertainties that could cause actual events and results to differ materially from those contained in the forward-looking statements. If any of these risks materialize or our assumptions prove incorrect, actual events and results could differ materially from those contained in the forward-looking statements. There may be additional risks that neither Corebridge nor Equitable Holdings presently know or that Corebridge and Equitable Holdings currently believe are immaterial that could also cause actual events and results to differ materially from those contained in the forward-looking statements. In addition, forward-looking statements reflect Corebridge and Equitable Holdings’ expectations, plans or forecasts of future events and views as of the date of this press release. Corebridge and Equitable Holdings anticipate that subsequent events and developments will cause Corebridge and Equitable Holdings’ assessments to change. While Corebridge and Equitable Holdings may elect to update these forward-looking statements at some point in the future, Corebridge and Equitable Holdings specifically disclaim any obligation to do so, unless required by applicable law. Neither Corebridge nor Equitable Holdings gives any assurance that Corebridge, Equitable Holdings or their new parent company will achieve the results or other matters set forth in the forward-looking statements.

No Offer or Solicitation

This press release is not intended to and shall not constitute an offer to sell or the solicitation of an offer to sell or the solicitation of an offer to buy any securities, or a solicitation of any vote or approval, nor shall there be any sale of securities in any jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such jurisdiction. No offer of securities shall be made except by means of a prospectus meeting the requirements of Section 10 of the Securities Act of 1933, as amended (the “Securities Act”), or in a transaction exempt from the registration requirements of the Securities Act.

Important Information and Where to Find It

This press release relates to the Proposed Transaction, which is the subject of a Registration Statement on Form S-4 filed by the new parent company with the SEC. The Registration Statement includes a joint proxy statement of Corebridge and Equitable Holdings that also constitutes a prospectus of the new parent company. After the Registration Statement has been declared effective, the definitive joint proxy statement/prospectus will be mailed to the stockholders of each of Corebridge and Equitable Holdings. This press release is not a substitute for the Registration Statement that the new parent company has filed with the SEC or any other documents that may be sent to Corebridge’s stockholders or Equitable Holdings’ stockholders in connection with the Proposed Transaction.

INVESTORS AND SECURITY HOLDERS ARE URGED TO READ THE REGISTRATION STATEMENT ON FORM S-4 AND THE JOINT PROXY STATEMENT/PROSPECTUS , AS WELL AS ANY OTHER RELEVANT DOCUMENTS FILED WITH, OR FURNISHED TO, THE SEC IN CONNECTION WITH THE PROPOSED TRANSACTION OR INCORPORATED BY REFERENCE INTO THE JOINT PROXY STATEMENT/PROSPECTUS, BECAUSE THEY CONTAIN OR WILL CONTAIN IMPORTANT INFORMATION REGARDING COREBRIDGE, EQUITABLE HOLDINGS, THEIR NEW PARENT COMPANY, THE PROPOSED TRANSACTION AND RELATED MATTERS.

Investors and security holders may obtain free copies of these documents and other documents filed with the SEC by Corebridge or Equitable Holdings through the website maintained by the SEC at http://www.sec.gov, or from Corebridge at its website, https://www.corebridgefinancial.com, or from Equitable Holdings at its website, https://equitableholdings.com (information included on or accessible through either of Corebridge or Equitable Holdings’ website is not incorporated by reference into this press release).

Participants in the Solicitation

Corebridge and Equitable Holdings and their respective directors and executive officers may be deemed to be participants in the solicitation of proxies from Corebridge’s stockholders or Equitable Holdings’ stockholders in connection with the Proposed Transaction under the rules of the SEC. Information about the directors and executive officers of Corebridge, including a description of their direct or indirect interests, by security holdings or otherwise, is set forth in Corebridge’s definitive proxy statement for its 2025 Annual Meeting of Stockholders, which was filed with the SEC on April 16, 2025, including under the headings “Compensation Discussion and Analysis,” “Compensation Tables” and “Security Ownership of 5% Beneficial Owners, Directors and Executive Officers.” To the extent holdings of Corebridge’s common stock by the directors and executive officers of Corebridge have changed or do change from the amounts of Corebridge’s common stock held by such persons as reflected therein, such changes have been or will be reflected on Initial Statements of Beneficial Ownership of Securities on Form 3 (“Form 3”), Statements of Changes in Beneficial Ownership on Form 4 (“Form 4”) or Annual Statements of Changes in Beneficial Ownership of Securities on Form 5 (“Form 5”), in each case filed with the SEC. Information about the directors and executive officers of Equitable Holdings, including a description of their direct or indirect interests, by security holdings or otherwise, is set forth in Equitable Holdings’ definitive proxy statement for its 2025 Annual Meeting of Stockholders, which was filed with the SEC on April 4, 2025, including under the headings “Executive Compensation” and “Certain Relationships and Related Person Transactions.” To the extent holdings of Equitable Holdings’ common stock by the directors and executive officers of Equitable Holdings have changed or do change from the amounts of Equitable Holdings’ common stock held by such persons as reflected therein, such changes have been or will be reflected on Forms 3, Forms 4 or Forms 5, in each case filed with the SEC. Other information regarding persons who may, under the rules of the SEC, be deemed participants in the proxy solicitation of Corebridge or Equitable Holdings’ stockholders in connection with the Proposed Transaction and a description of their direct and indirect interests, by security holdings or otherwise, is included in the Registration Statement. You may obtain free copies of these documents at the SEC’s website at www.sec.gov. Copies of documents filed with the SEC by Corebridge or Equitable Holdings will also be available free of charge from Corebridge or Equitable Holdings using the contact information above.

More News From Equitable Holdings, Inc. and Corebridge Financial, Inc.
2026-06-12 16:37 1mo ago
2026-05-20 16:15 2mo ago
Equitable Holdings Increases Common Stock Dividend and Declares Preferred Stock Dividends
EQH Axa Equitable Holdings
FMP Stock News
Original source text
NEW YORK--(BUSINESS WIRE)--Equitable Holdings, Inc. (NYSE: EQH), the leading financial services holding company of Equitable, AllianceBernstein and Equitable Advisors, announced today that its Board of Directors has declared a quarterly cash dividend of $0.30 per share of common stock. The dividend on the common stock will be payable June 8, 2026, to shareholders of record at the close of business on June 1, 2026.

The Company’s board also declared the following cash dividends:

Quarterly dividend of $328.125 per share on Series A 5.25% Non-Cumulative Perpetual Preferred Stock, with a liquidation preference of $25,000 per share, which are represented by depositary shares (NYSE: EQH PR A), each representing a 1/1,000th interest in a share of preferred stock, holders of which will receive $0.328125 per depositary share. The dividend will be payable on June 15, 2026, to holders of record as of June 4, 2026. Quarterly dividend of $268.750 per share on Series C 4.30% Non-Cumulative Perpetual Preferred Stock, with a liquidation preference of $25,000 per share, which are represented by depositary shares (NYSE: EQH PR C), each representing a 1/1,000th interest in a share of preferred stock, holders of which will receive $0.26875 per depositary share. The dividend will be payable on June 15, 2026, to holders of record as of June 4, 2026. About Equitable Holdings

Equitable Holdings, Inc. (NYSE: EQH) is a leading financial services holding company comprised of complementary and well-established businesses, Equitable, AllianceBernstein and Equitable Advisors. Equitable Holdings has $1.1 trillion in assets under management and administration (as of 3/31/2026) and more than 5 million client relationships globally. Founded in 1859, Equitable provides retirement and protection strategies to individuals, families and small businesses. AllianceBernstein is a global investment management firm that offers diversified investment services to institutional investors, individuals and private wealth clients. Equitable Advisors, LLC (Equitable Financial Advisors in MI and TN) has approximately 4,600 duly registered and licensed financial professionals that provide financial planning, wealth management, retirement planning, protection and risk management services to clients across the country.

Reference to the 1859 founding applies specifically and exclusively to Equitable Financial Life Insurance Company (NY, NY).

More News From Equitable Holdings, Inc.
2026-06-12 16:37 1mo ago
2026-05-21 12:21 2mo ago
Equitable Holdings Raises Dividend 11% Amid Strong Cash Flow Growth
EQH Axa Equitable Holdings
FMP Stock News
Original source text
Key Takeaways Equitable Holdings raised its quarterly dividend 11.1% to 30 cents per share, payable June 8.EQH posted $499M in Q1 operating cash flow, up sharply from $158M a year earlier.Equitable plans to merge with Corebridge in a deal creating $1.5T in assets under management. Equitable Holdings, Inc. (EQH - Free Report) recently approved an 11.1% increase in its quarterly dividend, raising the payout to 30 cents per share from 27 cents earlier. The dividend will be paid on June 8, 2026, to shareholders on record as of June 1. At the new annualized rate of $1.20 per share, the stock offers a dividend yield of 2.83%, calculated based on the closing price on May 20, which is comfortably above the industry average of 2.51%.

The company also declared preferred stock dividends, including $328.13 per share on its Series A 5.25% Non-Cumulative Perpetual Preferred Stock and $268.75 per share on its Series C 4.30% Non-Cumulative Perpetual Preferred Stock.

Equitable Holdings’ balance sheet continues to support its shareholder-friendly approach. The company ended the first quarter of 2026 with nearly $131.6 billion in investments and cash, while long-term debt remained relatively modest at $3.8 billion. Operating cash flow came in at $499 million during the quarter, sharply higher than the $158 million reported a year earlier.

Shareholder returns remained a priority in the March quarter. Equitable Holdings paid $76 million in cash dividends and bought back $147 million worth of shares. Management continues to target a 60-70% payout ratio of non-GAAP operating earnings in 2026.

Beyond capital returns, EQH is preparing for a transformative combination with Corebridge Financial, Inc. (CRBG - Free Report) . The all-stock merger, announced in March, is expected to create a company with nearly $1.5 trillion in assets under management. The combined entity will retain the Equitable name, trade under the EQH ticker on the NYSE, and be headquartered in Houston.

EQH’s Price PerformanceShares of Equitable Holdings have declined 11% in the year-to-date period, underperforming the industry’s 3.7% fall.

Image Source: Zacks Investment Research

Zacks Rank & Key PicksEquitable Holdings currently has a Zacks Rank #5 (Strong Sell).

Investors interested in the broader Finance space can look at some better-ranked stocks like Slide Insurance Holdings, Inc. (SLDE - Free Report) and CNO Financial Group, Inc. (CNO - Free Report) , each carrying a Zacks Rank #2 (Buy). You can see the complete list of today’s Zacks #1 Rank (Strong Buy) stocks here.

The Zacks Consensus Estimate for Slide Insurance’s 2026 earnings indicates 4.5% year-over-year growth. It has witnessed two upward estimate revisions in the past month against no downward movement. It beat earnings estimates in each of the past four quarters, with an average surprise of 41.8%. Furthermore, the consensus estimate for Slide Insurance’s 2026 revenues implies 25.9% year-over-year growth.

The consensus mark for CNO Financial’s 2026 full-year earnings indicates 6.9% year-over-year growth. It beat earnings estimates in each of the past four quarters, with an average surprise of 16.9%. Also, the consensus mark for CNO Financial’s 2026 revenues is pegged at $3.99 billion.
2026-06-12 16:37 1mo ago
2026-04-24 03:44 3mo ago
Farther Finance Advisors LLC Purchases 11,546 Shares of Arrowhead Pharmaceuticals, Inc. $ARWR
ARWR Arrowhead Pharmaceuticals
FMP Stock News
Original source text
Posted by Defense World Staff on Apr 24th, 2026

Farther Finance Advisors LLC grew its position in shares of Arrowhead Pharmaceuticals, Inc. (NASDAQ:ARWR – Free Report) by 2,923.0% in the fourth quarter, according to the company in its most recent 13F filing with the Securities & Exchange Commission. The fund owned 11,941 shares of the biotechnology company’s stock after acquiring an additional 11,546 shares during the quarter. Farther Finance Advisors LLC’s holdings in Arrowhead Pharmaceuticals were worth $793,000 at the end of the most recent reporting period.

Several other hedge funds also recently made changes to their positions in the business. Vanguard Group Inc. lifted its position in shares of Arrowhead Pharmaceuticals by 3.3% in the third quarter. Vanguard Group Inc. now owns 16,035,870 shares of the biotechnology company’s stock worth $553,077,000 after purchasing an additional 510,798 shares in the last quarter. Avoro Capital Advisors LLC grew its position in Arrowhead Pharmaceuticals by 2.8% in the third quarter. Avoro Capital Advisors LLC now owns 10,900,000 shares of the biotechnology company’s stock valued at $375,941,000 after purchasing an additional 300,000 shares in the last quarter. Arrowstreet Capital Limited Partnership increased its stake in Arrowhead Pharmaceuticals by 3,142.5% in the 3rd quarter. Arrowstreet Capital Limited Partnership now owns 2,081,689 shares of the biotechnology company’s stock valued at $71,797,000 after buying an additional 2,017,489 shares during the last quarter. Goldman Sachs Group Inc. lifted its position in Arrowhead Pharmaceuticals by 34.6% during the 1st quarter. Goldman Sachs Group Inc. now owns 1,741,666 shares of the biotechnology company’s stock worth $22,189,000 after buying an additional 447,456 shares in the last quarter. Finally, Baker BROS. Advisors LP lifted its position in Arrowhead Pharmaceuticals by 77.9% during the 3rd quarter. Baker BROS. Advisors LP now owns 1,670,762 shares of the biotechnology company’s stock worth $57,625,000 after buying an additional 731,588 shares in the last quarter. 62.61% of the stock is owned by institutional investors.

Insider Activity In other news, insider James C. Hamilton sold 10,000 shares of the firm’s stock in a transaction that occurred on Thursday, March 5th. The stock was sold at an average price of $64.19, for a total value of $641,900.00. Following the completion of the sale, the insider directly owned 236,958 shares of the company’s stock, valued at $15,210,334.02. This trade represents a 4.05% decrease in their ownership of the stock. The transaction was disclosed in a filing with the SEC, which is available at this link. 3.60% of the stock is currently owned by insiders.

Analyst Ratings Changes Several brokerages have recently weighed in on ARWR. HC Wainwright restated a “buy” rating and issued a $100.00 price objective on shares of Arrowhead Pharmaceuticals in a report on Wednesday, March 25th. Morgan Stanley upgraded Arrowhead Pharmaceuticals from an “equal weight” rating to an “overweight” rating and upped their target price for the stock from $78.00 to $100.00 in a report on Tuesday. Weiss Ratings raised Arrowhead Pharmaceuticals from a “sell (d-)” rating to a “hold (c-)” rating in a research report on Friday, February 6th. Piper Sandler restated an “overweight” rating and issued a $110.00 price target (up from $100.00) on shares of Arrowhead Pharmaceuticals in a research note on Tuesday, January 13th. Finally, Chardan Capital boosted their price target on Arrowhead Pharmaceuticals from $60.00 to $80.00 and gave the stock a “buy” rating in a research report on Wednesday, January 7th. One analyst has rated the stock with a Strong Buy rating, seven have given a Buy rating and three have given a Hold rating to the stock. According to MarketBeat.com, Arrowhead Pharmaceuticals has a consensus rating of “Moderate Buy” and a consensus price target of $83.78.

Get Our Latest Stock Report on ARWR

Arrowhead Pharmaceuticals Stock Up 0.6% Arrowhead Pharmaceuticals stock opened at $74.40 on Friday. The company has a debt-to-equity ratio of 0.29, a current ratio of 3.38 and a quick ratio of 3.38. The company’s 50-day moving average is $62.63 and its 200-day moving average is $57.95. The firm has a market capitalization of $10.42 billion, a PE ratio of 48.63 and a beta of 1.26. Arrowhead Pharmaceuticals, Inc. has a fifty-two week low of $12.44 and a fifty-two week high of $76.76.

Arrowhead Pharmaceuticals (NASDAQ:ARWR – Get Free Report) last issued its earnings results on Thursday, February 5th. The biotechnology company reported $0.22 earnings per share (EPS) for the quarter, missing the consensus estimate of $0.60 by ($0.38). Arrowhead Pharmaceuticals had a net margin of 18.54% and a return on equity of 35.64%. The firm had revenue of $264.03 million during the quarter, compared to analyst estimates of $225.66 million. During the same quarter last year, the business posted ($1.39) earnings per share. The company’s revenue for the quarter was up 10461.3% on a year-over-year basis. Sell-side analysts anticipate that Arrowhead Pharmaceuticals, Inc. will post -3.37 earnings per share for the current year.

Arrowhead Pharmaceuticals Profile (Free Report)

Arrowhead Pharmaceuticals, Inc is a clinical-stage biopharmaceutical company focused on the discovery, development and commercialization of RNA interference (RNAi) therapeutics. Since its founding in 2008, Arrowhead has leveraged its proprietary delivery platform—known internally as the Advanced RNAi Compound (ARC) technology—to silence disease-causing genes in patients suffering from genetically defined diseases. The company’s approach aims to offer durable, targeted treatments across a range of therapeutic areas.

The company’s pipeline includes multiple candidates in various stages of development.

Read More Five stocks we like better than Arrowhead Pharmaceuticals Want to see what other hedge funds are holding ARWR? Visit HoldingsChannel.com to get the latest 13F filings and insider trades for Arrowhead Pharmaceuticals, Inc. (NASDAQ:ARWR – Free Report).

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2026-06-12 16:37 1mo ago
2026-04-24 06:39 3mo ago
Arrowhead Pharmaceuticals Receives Positive CHMP Opinion Recommending Approval of REDEMPLO® (plozasiran) to Reduce Triglycerides in Adults with Familial Chylomicronemia Syndrome (FCS) in Europe
ARWR Arrowhead Pharmaceuticals
FMP Stock News
Original source text
– If confirmed by the European Commission, REDEMPLO would be the first and only siRNA medicine authorized in the EU for both genetically confirmed and clinically diagnosed adult patients with FCS

– People living with FCS have extremely high triglyceride levels and a substantially higher risk of acute pancreatitis and related long-term complications, often resulting in a reduced quality of life

– The CHMP opinion is based on positive results from the Phase 3 PALISADE study where REDEMPLO reduced triglycerides by a median of 80% from baseline and significantly fewer cases of acute pancreatitis were seen in patients using REDEMPLO compared with those using placebo

PASADENA, Calif.--(BUSINESS WIRE)--Arrowhead Pharmaceuticals, Inc. (NASDAQ: ARWR) today announced that the European Medicines Agency’s Committee for Medicinal Products for Human Use (EMA CHMP) has adopted a positive opinion, recommending the approval of REDEMPLO® (plozasiran), a small interfering RNA (siRNA) medicine, as an adjunct to diet to reduce triglyceride levels in adult patients with familial chylomicronemia syndrome (FCS). FCS remains widely underdiagnosed and affects an estimated 1 to 13 people per million globally. This rare disease is characterized by triglyceride levels that can be orders of magnitude higher than normal, leading to a substantially higher risk of developing acute, recurrent, and potentially fatal pancreatitis.

We are pleased with the CHMP’s recommendation, which brings us closer to potential approval of REDEMPLO as a new treatment option for people living with genetically or clinically confirmed FCS across Europe

Share The European Commission is expected to issue a decision on REDEMPLO’s Marketing Authorization in the second quarter of 2026. If approved, REDEMPLO will be the first and only siRNA medicine authorized in the European Union for both genetically confirmed and clinically diagnosed adult patients with FCS. This recommendation follows approvals in the United States, Canada, and China, as Arrowhead continues its efforts to increase global access to care for people living with FCS.

In a press release announcing the positive opinion, EMA stated, "Although other authorised medicines can help people with FCS confirmed by genetic testing, REDEMPLO does not require genetic confirmation of the condition, thus providing a treatment option for more adults with FCS and addressing the unmet medical need in these patients."

“We are pleased with the CHMP’s recommendation, which brings us closer to potential approval of REDEMPLO as a new treatment option for people living with genetically or clinically confirmed FCS across Europe,” said Christopher Anzalone, Ph.D., President and CEO at Arrowhead Pharmaceuticals. “This milestone reflects the strength of the clinical data and the ability of our TRiM™ platform to enable targeted siRNA therapies to potentially reach multiple tissues and disease areas. We believe REDEMPLO could represent an important new option for the FCS community in Europe, and we are working with regulators and the healthcare community to bring this therapy to more patients as quickly as possible.”

Harnessing Arrowhead’s proprietary Targeted RNAi Molecule (TRiM™) platform, REDEMPLO is designed to silence the mRNA encoding apolipoprotein C-III (apoC-III). ApoC-III is a key regulator of triglyceride metabolism that inhibits triglyceride catabolism and clearance, resulting in elevated triglyceride levels. Individuals with genetic loss-of-function variants in APOC3 typically have markedly lower triglyceride levels and a reduced risk of atherosclerotic cardiovascular disease.

The CHMP positive opinion was supported by clinical data from the Phase 3 PALISADE study, a randomized, double-blind, placebo-controlled trial in adults with clinically diagnosed or genetically confirmed FCS. The PALISADE study met its primary endpoint and all multiplicity-controlled key secondary endpoints, including demonstrating significant reductions in triglycerides and apoC-III and in the incidence of acute pancreatitis in the pooled dose groups. In PALISADE, 25 mg REDEMPLO reduced triglycerides by a median of 80% from baseline versus a 17% reduction with placebo and significantly fewer cases of acute pancreatitis were seen in patients using REDEMPLO compared with those using placebo. REDEMPLO is self-administered via subcutaneous injection once every three months.1,2

The most common adverse reactions are hyperglycaemia (12.8%), headache (6.8%), nausea (4.7%), and injection site reaction (4.7%).

“Patients with FCS face a substantial burden of disease and are at life-long risk of acute pancreatitis, with few effective treatment options available,” said Gerald F Watts, DSc, PhD, MD, FRCP, Professor of Cardio-metabolic Medicine, University of Western Australia. “The results from the PALISADE study demonstrate that plozasiran can achieve substantial and sustained reductions in triglycerides in patients with FCS. These data highlight the potential of targeted RNA interference approaches in addressing conditions like FCS that have so far been difficult to treat. Plozasiran is a major advance in the care of FCS and a significant step toward expanding treatment options for patients across Europe.”

The efficacy and safety results from the PALISADE study were presented at the European Society of Cardiology (ESC) Congress 2024 and the American Heart Association Scientific Sessions 2024 (AHA24) and simultaneously published in The New England Journal of Medicine and Circulation, respectively. ESC, AHA24, and other plozasiran presentations may be accessed on the Events and Presentations page in the Investors section of the Arrowhead website.

REDEMPLO has been granted Orphan Designation by the EMA for the treatment of patients with FCS, and Breakthrough Therapy Designation, Fast Track Designation, and Orphan Drug Designation by the U.S. FDA for the treatment of patients with FCS.

About FCS

Familial chylomicronemia syndrome (FCS) is a severe and rare disease leading to extremely high triglyceride (TG) levels, typically over 10 mmol/L (880 mg/dL). Such severe elevations can lead to various serious signs and symptoms including acute and potentially fatal pancreatitis, chronic abdominal pain, diabetes, hepatic steatosis, and cognitive issues. Currently, there are limited therapeutic options to adequately treat FCS.

About the PALISADE Phase 3 Study

The PALISADE study (NCT05089084) was a Phase 3 placebo-controlled study to evaluate the efficacy and safety of plozasiran in adults with genetically confirmed or clinically diagnosed FCS. The primary endpoint of the study was percent change from baseline in fasting TG versus placebo at Month 10. A total of 75 subjects distributed across 39 different sites in 18 countries were randomized to receive 25 mg plozasiran, 50 mg plozasiran, or matching placebo once every three months. Participants who completed the randomized period were eligible to continue in a 2-part extension period, where all participants receive plozasiran.

About REDEMPLO® (plozasiran)

REDEMPLO (plozasiran) is the first and only siRNA treatment approved in these countries that has been studied in both genetically confirmed and clinically diagnosed patients living with FCS. REDEMPLO is a first-in-class siRNA therapeutic designed to suppress the production of apoC-III, a protein produced in the liver that raises triglyceride levels by slowing their breakdown and clearance. By targeting apoC-III with sustained silencing, REDEMPLO delivers significant reductions in triglyceride levels. REDEMPLO is self-administered via subcutaneous injection once every three months.

The EMA CHMP has adopted a positive opinion recommending the European Marketing Authorization of REDEMPLO (plozasiran), which is already approved by the U.S. Food and Drug Administration, Health Canada, and China’s National Medical Products Administration as an adjunct to diet to reduce triglycerides for adults with Familial Chylomicronemia Syndrome (FCS).

In addition to approvals of REDEMPLO in the U.S., Canada, and China, plozasiran has been submitted to additional global regulatory authorities for review and marketing authorization. Plozasiran is also being investigated in the SHASTA-3 (NCT06347003), SHASTA-4 (NCT06347016), and SHASTA-5 (NCT06880770) Phase 3 studies in adults with severe hypertriglyceridemia and the MUIR-3 (NCT06347133) Phase 3 study in adults with hypertriglyceridemia. In December 2025, plozasiran was granted Breakthrough Therapy designation by the U.S. FDA in severe hypertriglyceridemia.

About Arrowhead Pharmaceuticals

Arrowhead Pharmaceuticals (NASDAQ: ARWR) is a commercial-stage pharmaceutical company developing medicines that treat intractable diseases by silencing the genes that cause them, harnessing the natural RNA interference (RNAi) mechanism. The company has built a broad portfolio of clinical and commercial RNAi therapeutics through its industry-leading targeted RNAi molecule (TRiM™) platform, which can precisely silence genes in a wide range of cell types, including liver, lung, muscle, adipose, and central nervous system tissue. At Arrowhead, we rapidly advance potential best- and first-in-class RNAi treatments for diseases with significant unmet medical need, because every day matters to the patients we serve.

For more information, please visit www.arrowheadpharma.com, or follow us on X (formerly Twitter) at @ArrowheadPharma, LinkedIn, Facebook, and Instagram. To be added to the Company’s email list and receive news directly, please visit http://ir.arrowheadpharma.com/email-alerts.

Safe Harbor Statement under the Private Securities Litigation Reform Act:

This news release contains forward-looking statements within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995. Any statements contained in this release except for historical information may be deemed to be forward-looking statements. Without limiting the generality of the foregoing, words such as “may,” “will,” “expect,” “believe,” “anticipate,” “hope,” “intend,” “plan,” “project,” “could,” “estimate,” “continue,” “target,” “forecast” or “continue” or the negative of these words or other variations thereof or comparable terminology are intended to identify such forward-looking statements. In addition, any statements that refer to projections of our future financial performance, trends in our business, expectations for our product pipeline, products or product candidates or other characterizations of future events or circumstances are forward-looking statements. These forward-looking statements include, but are not limited to, statements about our beliefs and expectations regarding the long-term impacts of REDEMPLO (plozasiran) on patient health and the health care system; our beliefs and expectations regarding the pricing, value, or expected timing for availability of our drugs and drug candidates if approved; and our beliefs and expectations around the potential uses and value of the TRiM™ platform. These statements are based upon our current expectations and speak only as of the date hereof. Actual results or outcomes may differ materially and adversely from those expressed in any forward-looking statements as a result of numerous factors and uncertainties, including the safety and efficacy of our products and product candidates, pricing and reimbursement decisions related to our products if approved, demand for our products, decisions of regulatory authorities and the timing thereof, the duration and impact of regulatory delays in our clinical programs, our ability to finance our operations, the likelihood and timing of the receipt of future milestone and licensing fees, the future success of our scientific studies, the timing for starting and completing clinical trials, rapid technological change in our markets, the enforcement of our intellectual property rights, and the other risks and uncertainties described in our most recent Annual Report on Form 10-K, subsequent Quarterly Reports on Form 10-Q and other documents filed with the Securities and Exchange Commission from time to time. We assume no obligation to update or revise forward-looking statements to reflect new events or circumstances.

Source: Arrowhead Pharmaceuticals, Inc.

1 Watts GF, Rosenson RS, Hegele RA, Goldberg IJ, Gallo A, Mertens A, Baass A, Zhou R, Muhsin M, Hellawell J, et al. Plozasiran for managing persistent chylomicronemia and pancreatitis risk. N Engl J Med. 2024;392:127–137. https://doi.org/10.1056/nejmoa2409368 PMID: 39225259
2 Watts GF, Hegele RA, Rosenson RS et al. Temporal Effects of Plozasiran on Lipids and Lipoproteins in Persistent Chylomicronemia. Circulation. 2025:151(10); 733-736; https://doi.org/10.1161/CIRCULATIONAHA.124.072860 PMID:39549263

More News From Arrowhead Pharmaceuticals, Inc.
2026-06-12 16:37 1mo ago
2026-04-27 03:46 3mo ago
B. Metzler seel. Sohn & Co. AG Takes $1.37 Million Position in Arrowhead Pharmaceuticals, Inc. $ARWR
ARWR Arrowhead Pharmaceuticals
FMP Stock News
Original source text
Posted by Defense World Staff on Apr 27th, 2026

B. Metzler seel. Sohn & Co. AG purchased a new stake in Arrowhead Pharmaceuticals, Inc. (NASDAQ:ARWR – Free Report) during the fourth quarter, according to its most recent 13F filing with the Securities & Exchange Commission. The fund purchased 20,695 shares of the biotechnology company’s stock, valued at approximately $1,374,000.

Other institutional investors also recently modified their holdings of the company. M&T Bank Corp lifted its holdings in shares of Arrowhead Pharmaceuticals by 2,569.6% in the fourth quarter. M&T Bank Corp now owns 240,634 shares of the biotechnology company’s stock valued at $15,976,000 after purchasing an additional 231,620 shares in the last quarter. Nordea Investment Management AB lifted its holdings in shares of Arrowhead Pharmaceuticals by 74.5% in the third quarter. Nordea Investment Management AB now owns 372,282 shares of the biotechnology company’s stock valued at $12,661,000 after purchasing an additional 158,937 shares in the last quarter. HBK Sorce Advisory LLC acquired a new stake in shares of Arrowhead Pharmaceuticals in the third quarter valued at about $2,823,000. Erste Asset Management GmbH increased its position in shares of Arrowhead Pharmaceuticals by 55.3% in the third quarter. Erste Asset Management GmbH now owns 73,000 shares of the biotechnology company’s stock valued at $2,466,000 after acquiring an additional 26,000 shares during the last quarter. Finally, Vanguard Personalized Indexing Management LLC acquired a new stake in shares of Arrowhead Pharmaceuticals in the third quarter valued at about $287,000. 62.61% of the stock is currently owned by institutional investors.

Wall Street Analyst Weigh In ARWR has been the topic of a number of recent research reports. Piper Sandler reaffirmed an “overweight” rating and issued a $110.00 target price (up from $100.00) on shares of Arrowhead Pharmaceuticals in a research report on Tuesday, January 13th. HC Wainwright reaffirmed a “buy” rating and issued a $100.00 target price on shares of Arrowhead Pharmaceuticals in a research report on Wednesday, March 25th. Chardan Capital lifted their target price on Arrowhead Pharmaceuticals from $60.00 to $80.00 and gave the company a “buy” rating in a research report on Wednesday, January 7th. B. Riley Financial lifted their target price on Arrowhead Pharmaceuticals from $61.00 to $101.00 and gave the company a “buy” rating in a research report on Thursday, January 22nd. Finally, The Goldman Sachs Group lifted their target price on Arrowhead Pharmaceuticals from $50.00 to $85.00 and gave the company a “neutral” rating in a research report on Wednesday, January 7th. One research analyst has rated the stock with a Strong Buy rating, seven have issued a Buy rating and three have issued a Hold rating to the stock. Based on data from MarketBeat.com, the stock has a consensus rating of “Moderate Buy” and an average price target of $83.78.

Read Our Latest Research Report on ARWR

Arrowhead Pharmaceuticals Price Performance NASDAQ:ARWR opened at $73.91 on Monday. The company has a debt-to-equity ratio of 0.29, a quick ratio of 3.38 and a current ratio of 3.38. The stock’s 50-day simple moving average is $62.83 and its 200 day simple moving average is $58.51. The company has a market cap of $10.35 billion, a P/E ratio of 48.31 and a beta of 1.26. Arrowhead Pharmaceuticals, Inc. has a 52-week low of $12.44 and a 52-week high of $76.76.

Arrowhead Pharmaceuticals (NASDAQ:ARWR – Get Free Report) last announced its quarterly earnings results on Thursday, February 5th. The biotechnology company reported $0.22 earnings per share for the quarter, missing analysts’ consensus estimates of $0.60 by ($0.38). The business had revenue of $264.03 million for the quarter, compared to analyst estimates of $225.66 million. Arrowhead Pharmaceuticals had a return on equity of 35.64% and a net margin of 18.54%.Arrowhead Pharmaceuticals’s quarterly revenue was up 10461.3% compared to the same quarter last year. During the same period last year, the firm earned ($1.39) EPS. As a group, sell-side analysts forecast that Arrowhead Pharmaceuticals, Inc. will post -3.37 EPS for the current fiscal year.

Insider Buying and Selling In other Arrowhead Pharmaceuticals news, CFO Daniel Joseph Apel sold 13,095 shares of the business’s stock in a transaction that occurred on Wednesday, April 22nd. The stock was sold at an average price of $71.35, for a total transaction of $934,328.25. Following the transaction, the chief financial officer owned 162,905 shares of the company’s stock, valued at $11,623,271.75. The trade was a 7.44% decrease in their ownership of the stock. The sale was disclosed in a filing with the Securities & Exchange Commission, which is available through this hyperlink. The transaction was executed under a pre-arranged Rule 10b5-1 trading plan. The sale was made to cover tax withholding obligations related to the vesting of equity awards. Also, insider James C. Hamilton sold 10,000 shares of the business’s stock in a transaction that occurred on Thursday, April 23rd. The stock was sold at an average price of $75.00, for a total value of $750,000.00. Following the transaction, the insider directly owned 226,958 shares in the company, valued at approximately $17,021,850. This trade represents a 4.22% decrease in their position. The SEC filing for this sale provides additional information. The transaction was executed under a pre-arranged Rule 10b5-1 trading plan. In the last three months, insiders have sold 33,095 shares of company stock worth $2,326,228. Company insiders own 3.60% of the company’s stock.

About Arrowhead Pharmaceuticals (Free Report)

Arrowhead Pharmaceuticals, Inc is a clinical-stage biopharmaceutical company focused on the discovery, development and commercialization of RNA interference (RNAi) therapeutics. Since its founding in 2008, Arrowhead has leveraged its proprietary delivery platform—known internally as the Advanced RNAi Compound (ARC) technology—to silence disease-causing genes in patients suffering from genetically defined diseases. The company’s approach aims to offer durable, targeted treatments across a range of therapeutic areas.

The company’s pipeline includes multiple candidates in various stages of development.

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2026-06-12 16:37 1mo ago
2026-05-01 07:30 2mo ago
Arrowhead Pharmaceuticals Receives TGA Approval of REDEMPLO® (plozasiran) in Australia, Expanding Global Access for Patients with Familial Chylomicronemia Syndrome (FCS)
ARWR Arrowhead Pharmaceuticals
FMP Stock News
Original source text
– REDEMPLO is the first and only medicine approved for use in the treatment of FCS in Australia, and is authorized for both genetically confirmed and clinically diagnosed adult patients with FCS

– People living with FCS have extremely high triglyceride levels and a substantially higher risk of acute pancreatitis and related long-term complications, often resulting in a reduced quality of life

– The approval in Australia is based on positive results from the Phase 3 PALISADE study where REDEMPLO reduced triglycerides by a median of 80% from baseline and significantly reduced the incidence of acute pancreatitis across pooled doses, as compared with those using placebo

PASADENA, Calif.--(BUSINESS WIRE)--Arrowhead Pharmaceuticals, Inc. (NASDAQ: ARWR) today announced that the Australian Therapeutic Goods Administration (TGA) has approved REDEMPLO® (plozasiran), a small interfering RNA (siRNA) medicine, as an adjunct to diet to reduce triglyceride levels for adult patients with familial chylomicronemia syndrome (FCS) for whom standard triglyceride lowering therapies have been inadequate. FCS is a severe, rare disease characterized by triglyceride levels that can be orders of magnitude higher than normal, leading to a substantially higher risk of developing acute, recurrent, and potentially fatal pancreatitis. FCS remains widely underdiagnosed and affects an estimated 1 to 13 people per million globally.

We are pleased that REDEMPLO is now the first-ever approved treatment for Australians living with genetic or clinical FCS

Share REDEMPLO is the first and only medicine approved for use in the treatment of FCS in Australia, and is authorized for both genetically confirmed and clinically diagnosed adult patients with FCS. This approval by TGA follows approvals in the United States, Canada, and China, and a positive opinion recommending marketing authorization from EMA as Arrowhead continues its efforts to increase global access to care for people living with FCS.

“We are pleased that REDEMPLO is now the first-ever approved treatment for Australians living with genetic or clinical FCS,” said Christopher Anzalone, Ph.D., President and CEO of Arrowhead Pharmaceuticals. “This approval underscores the strength of the clinical data and the ability of our TRiM™ platform to develop targeted siRNA therapies to potentially reach multiple tissues and disease areas. We believe REDEMPLO could represent an important medicine for the FCS community in Australia, and we are working to bring this therapy to more patients as quickly as possible.”

Harnessing Arrowhead’s proprietary Targeted RNAi Molecule (TRiM™) platform, REDEMPLO is designed to silence the mRNA encoding apolipoprotein C-III (apoC-III). ApoC-III is a key regulator of triglyceride metabolism that inhibits triglyceride catabolism and clearance, resulting in elevated triglyceride levels. Individuals with genetic loss-of-function variants in APOC3 typically have markedly lower triglyceride levels and a reduced risk of atherosclerotic cardiovascular disease.

The Therapeutic Goods Administration approval was supported by clinical data from the Phase 3 PALISADE study, a randomized, double-blind, placebo-controlled trial in adults with clinically diagnosed or genetically confirmed FCS. The clinical study was conducted across 39 global sites, including 5 study locations in Australia. The PALISADE study met its primary endpoint and all multiplicity-controlled key secondary endpoints, including demonstrating significant reductions in triglycerides and apoC-III and in the incidence of acute pancreatitis in the pooled dose groups. In PALISADE, 25 mg REDEMPLO reduced triglycerides by a median of 80% from baseline versus a 17% reduction with placebo. Moreover, the odds of acute pancreatitis were 83% lower in the pooled dose groups (combined doses of 25 mg and 50 mg plozasiran) when compared with the placebo group (2 events in 2 subjects (4%) vs. 7 events in 5 subjects (20%), respectively). REDEMPLO is self-administered via subcutaneous injection once every three months.1,2

The Australian Product Information notes the most common adverse reaction is hyperglycaemia (12.8%). Other common adverse reactions include headache (6.8%), nausea (4.7%), and injection site reaction (4.7%).

“Patients with FCS face a substantial burden of disease and are at life-long risk of acute pancreatitis, with few effective treatment options available,” said Gerald F Watts, DSc, PhD, MD, FRCP, Professor of Cardio-metabolic Medicine, University of Western Australia. “The results from the PALISADE study demonstrate that plozasiran can achieve substantial and sustained reductions in triglycerides in patients with FCS. These data highlight the potential of targeted RNA interference approaches in addressing conditions like FCS that have so far been difficult to treat. Plozasiran is a major advance in the care of FCS and a significant step toward expanding treatment options for patients.”

The efficacy and safety results from the PALISADE study were presented at the European Society of Cardiology (ESC) Congress 2024 and the American Heart Association Scientific Sessions 2024 (AHA24) and simultaneously published in The New England Journal of Medicine and Circulation, respectively. ESC, AHA24, and other plozasiran presentations may be accessed on the Events and Presentations page in the Investors section of the Arrowhead website.

REDEMPLO was reviewed via the priority review pathway by Australia’s TGA and was granted Breakthrough Therapy Designation, Fast Track Designation, and Orphan Drug Designation by the U.S. FDA, as well as Orphan Medicinal Product Designation by the European Medicines Agency for the treatment of patients with FCS.

About FCS

Familial chylomicronemia syndrome (FCS) is a severe and rare disease leading to extremely high triglyceride (TG) levels, typically over 10 mmol/L (880 mg/dL). Such severe elevations can lead to various serious signs and symptoms including acute and potentially fatal pancreatitis, chronic abdominal pain, diabetes, hepatic steatosis, and cognitive issues. Currently, there are limited therapeutic options to adequately treat FCS.

About the PALISADE Phase 3 Study

The PALISADE study (NCT05089084) was a Phase 3 placebo-controlled study to evaluate the efficacy and safety of plozasiran in adults with genetically confirmed or clinically diagnosed FCS. The primary endpoint of the study was percent change from baseline in fasting TG versus placebo at Month 10. A total of 75 subjects distributed across 39 different sites in 18 countries were randomized to receive 25 mg plozasiran, 50 mg plozasiran, or matching placebo once every three months. Participants who completed the randomized period were eligible to continue in a 2-part extension period, where all participants receive plozasiran.

About REDEMPLO® (plozasiran)

REDEMPLO (plozasiran) is the first and only siRNA treatment approved in these countries that has been studied in both genetically confirmed and clinically diagnosed patients living with FCS. REDEMPLO is a first-in-class siRNA therapeutic designed to suppress the production of apoC-III, a protein produced in the liver that raises triglyceride levels by slowing their breakdown and clearance. By targeting apoC-III with sustained silencing, REDEMPLO delivers significant reductions in triglyceride levels. REDEMPLO is self-administered via subcutaneous injection once every three months.

The EMA CHMP has adopted a positive opinion recommending the European Marketing Authorization of REDEMPLO (plozasiran), which is already approved by the U.S. Food and Drug Administration, Health Canada, and China’s National Medical Products Administration as an adjunct to diet to reduce triglycerides for adults with Familial Chylomicronemia Syndrome (FCS).

Plozasiran is also being investigated in the SHASTA-3 (NCT06347003), SHASTA-4 (NCT06347016), and SHASTA-5 (NCT06880770) Phase 3 studies in adults with severe hypertriglyceridemia and the MUIR-3 (NCT06347133) Phase 3 study in adults with hypertriglyceridemia. In December 2025, plozasiran was granted Breakthrough Therapy designation by the U.S. FDA in severe hypertriglyceridemia.

About Arrowhead Pharmaceuticals

Arrowhead Pharmaceuticals (NASDAQ: ARWR) is a commercial-stage pharmaceutical company developing medicines that treat intractable diseases by silencing the genes that cause them, harnessing the natural RNA interference (RNAi) mechanism. The company has built a broad portfolio of clinical and commercial RNAi therapeutics through its industry-leading targeted RNAi molecule (TRiM™) platform, which can precisely silence genes in a wide range of cell types, including liver, lung, muscle, adipose, and central nervous system tissue. At Arrowhead, we rapidly advance potential best- and first-in-class RNAi treatments for diseases with significant unmet medical need, because every day matters to the patients we serve.

For more information, please visit arrowheadpharma.com, or follow us on X (formerly Twitter) at @ArrowheadPharma, LinkedIn, Facebook, and Instagram. To be added to the Company’s email list and receive news directly, please visit ir.arrowheadpharma.com/email-alerts.

Safe Harbor Statement under the Private Securities Litigation Reform Act:

This news release contains forward-looking statements within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995. Any statements contained in this release except for historical information may be deemed to be forward-looking statements. Without limiting the generality of the foregoing, words such as “may,” “will,” “expect,” “believe,” “anticipate,” “hope,” “intend,” “plan,” “project,” “could,” “estimate,” “continue,” “target,” “forecast” or “continue” or the negative of these words or other variations thereof or comparable terminology are intended to identify such forward-looking statements. In addition, any statements that refer to projections of our future financial performance, trends in our business, expectations for our product pipeline, products or product candidate or other characterizations of future events or circumstances are forward-looking statements. These forward-looking statements include, but are not limited to, statements about our beliefs and expectations regarding the long-term impacts of REDEMPLO (plozasiran) on patient health and the health care system; our beliefs and expectations regarding the pricing, value, or expected timing for availability of our drugs and drug candidates; and our beliefs and expectations around the potential uses and value of the TRiM™ platform. These statements are based upon our current expectations and speak only as of the date hereof. Actual results or outcomes may differ materially and adversely from those expressed in any forward-looking statements as a result of numerous factors and uncertainties, including but not limited to the safety and efficacy of our products and product candidates, pricing and reimbursement decisions related to our products, demand for our products, decisions of regulatory authorities and the timing thereof, the duration and impact of regulatory delays in our clinical programs, our ability to finance our operations, the likelihood and timing of the receipt of future milestone and licensing fees, the future success of our scientific studies, the timing for starting and completing clinical trials, rapid technological change in our markets, the enforcement of our intellectual property rights, and the other risks and uncertainties described in our most recent Annual Report on Form 10-K, subsequent Quarterly Reports on Form 10-Q and other documents filed with the Securities and Exchange Commission from time to time. We assume no obligation to update or revise forward-looking statements to reflect new events or circumstances.

Source: Arrowhead Pharmaceuticals, Inc.

More News From Arrowhead Pharmaceuticals, Inc.
2026-06-12 16:37 1mo ago
2026-05-04 07:30 2mo ago
Arrowhead Pharmaceuticals to Participate in Upcoming May 2026 Events
ARWR Arrowhead Pharmaceuticals
FMP Stock News
Original source text
PASADENA, Calif.--(BUSINESS WIRE)--Arrowhead Pharmaceuticals, Inc. (NASDAQ: ARWR) today announced that it is scheduled to participate in the following upcoming events:

BofA Securities 2026 Healthcare Conference – May 12-14, 2026

Type: Investor Group Dinner
Date/Time: May 12, 2026

Type: Fireside Chat Presentation
Date/Time: May 13, 2026, 10:00 am PDT

TIDES USA Oligonucleotide & Peptide Therapeutics – May 11-14 in Boston, Massachusetts

Title: Systemic RNAi Targeting MAPT: Advancing Tau Suppression Across the CNS with TRiM™ SC
Date/Time: May 13, 2026, 4:45 PM EDT
Presenter: Kayal Madhivanan

33rd European Congress on Obesity (ECO 2026) – May 12-15 in Istanbul, Türkiye

Title: Elevated Activin E levels correlate with insulin resistance and metabolic dysfunction in non-human primates and adult patients with obesity and type 2 diabetes
Date/Time: May 13-14; 1:00 PM – 3:00 PM
Presenter: Jane Kerr, MBChB, MPH, DRCOG

2026 RBC Capital Markets Global Healthcare Conference – May 19-20, 2026

Type: Fireside Chat Presentation
Date/Time: May 20, 2026, 9:00 am EDT

European Atherosclerosis Society (EAS 2026) Congress – May 24-27 in Athens, Greece

2 Oral Presentations:

Title: PHARMACOKINETICS, PHARMACODYNAMICS, AND SAFETY OF PLOZASIRAN IN SUBJECTS WITH RENAL OR HEPATIC IMPAIRMENT
Session: Late Breaker Clinical Abstracts
Date/Time: May 26, 2026, 5:00 AM – 5:15 PM
Presenter: Jennifer Hellawell, MD

Title: A CASE REPORT OF A PREGNANT WOMAN WITH FAMILIAL CHYLOMICRONEMIA SYNDROME TREATED WITH PLOZASIRAN, A SMALL INTERFERING RNA AGAINST APOC3
Session: EAS stage: Outreach and case presentations
Date/Time: May 26, 2026, 8:30 AM – 10:30 AM
Presenter: Ann Mertens, MD

European Association for the Study of the Liver (EASL 2026) – May 27-30 in Barcelona, Spain

Title: ARO‑INHBE demonstrates clinically meaningful reductions in liver fat as monotherapy and in combination with low-dose tirzepatide in adults with obesity
Late Breaker Poster Session
Presenter: Rinki Murphy, MBChB, PhD

Presentation materials and webcast links, if applicable, may be accessed on the Events and Presentations page under the Investors section of the Arrowhead website.

About Arrowhead Pharmaceuticals

Arrowhead Pharmaceuticals (NASDAQ: ARWR) is a commercial-stage pharmaceutical company developing medicines that treat intractable diseases by silencing the genes that cause them, harnessing the natural RNA interference (RNAi) mechanism. The company has built a broad portfolio of clinical and commercial RNAi therapeutics through its industry-leading targeted RNAi molecule (TRiM™) platform, which can precisely silence genes in a wide range of cell types, including liver, lung, muscle, adipose, and central nervous system tissue. At Arrowhead, we rapidly advance potential best- and first-in-class RNAi treatments for diseases with significant unmet medical need, because every day matters to the patients we serve.

For more information, please visit arrowheadpharma.com, or follow us on X (formerly Twitter) at @ArrowheadPharma, LinkedIn, Facebook, and Instagram. To be added to the Company’s email list and receive news directly, please visit ir.arrowheadpharma.com/email-alerts.

Safe Harbor Statement under the Private Securities Litigation Reform Act:

This news release contains forward-looking statements within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. Any statements contained in this release except for historical information may be deemed to be forward-looking statements. Without limiting the generality of the foregoing, words such as “may,” “will,” “expect,” “believe,” “anticipate,” “hope,” “intend,” “plan,” “project,” “could,” “estimate,” “continue,” “target,” “forecast” or “continue” or the negative of these words or other variations thereof or comparable terminology are intended to identify such forward-looking statements. In addition, any statements that refer to projections of our future financial performance, trends in our business, expectations for our product pipeline or product candidates, including anticipated regulatory submissions and clinical program results, prospects or benefits of our collaborations with other companies, or other characterizations of future events or circumstances are forward-looking statements. These forward-looking statements include, but are not limited to, statements about the initiation, timing, progress and results of our preclinical studies and clinical trials, and our research and development programs; our expectations regarding the potential benefits of the partnership, licensing and/or collaboration arrangements and other strategic arrangements and transactions we have entered into or may enter into in the future; our beliefs and expectations regarding milestone, royalty or other payments that could be due to or from third parties under existing agreements; and our estimates regarding future revenues, research and development expenses, capital requirements and payments to third parties. These statements are based upon our current expectations and speak only as of the date hereof. Our actual results may differ materially and adversely from those expressed in any forward-looking statements as a result of numerous factors and uncertainties, including the safety and efficacy of our product candidates, decisions of regulatory authorities and the timing thereof, the duration and impact of regulatory delays in our clinical programs, our ability to finance our operations, the likelihood and timing of the receipt of future milestone and licensing fees, the future success of our scientific studies, our ability to successfully develop and commercialize drug candidates, the timing for starting and completing clinical trials, rapid technological change in our markets, the enforcement of our intellectual property rights, and the other risks and uncertainties described in our most recent Annual Report on Form 10-K, subsequent Quarterly Reports on Form 10-Q and other documents filed with the Securities and Exchange Commission from time to time. We assume no obligation to update or revise forward-looking statements to reflect new events or circumstances.

Source: Arrowhead Pharmaceuticals, Inc.

More News From Arrowhead Pharmaceuticals, Inc.
2026-06-12 16:37 1mo ago
2026-05-07 16:01 2mo ago
Arrowhead Pharmaceuticals Reports Fiscal 2026 Second Quarter Results
ARWR Arrowhead Pharmaceuticals
FMP Stock News
Original source text
-

- Conference Call and Webcast Today, May 7, 2026, at 4:30 p.m. ET

PASADENA, Calif.--(BUSINESS WIRE)--Arrowhead Pharmaceuticals, Inc. (NASDAQ: ARWR) today announced financial results for its fiscal 2026 second quarter ended March 31, 2026. The Company is hosting a conference call today, May 7, 2026, at 4:30 p.m. ET to discuss the results.

Arrowhead continues to show strong execution in meeting and exceeding our commercial, R&D, and corporate goals.

Share “Arrowhead continues to show strong execution in meeting and exceeding our commercial, R&D, and corporate goals. The company is on extremely strong footing to continue to drive growth in the near-term with numerous opportunities to create long-term shareholder value,” said Christopher Anzalone, Ph.D., President and CEO at Arrowhead Pharmaceuticals. “We remain focused on a few key areas as being critical sources of sustainable growth for Arrowhead, and we have made tangible advancements across these areas. These include: strengthening our commercial presence to bring REDEMPLO® and potentially other cardiometabolic products in the future to the many patients and physicians who need it; continuing to deliver best-in-class in discovery, development, and regulatory capabilities in support of a deep pipeline of RNAi therapeutics capable of silencing genes expressed throughout the body to treat various diseases; and, being strategic and disciplined around pipeline, portfolio, and financial management.”

Key REDEMPLO® Commercial Events

Continued to build strong and consistent momentum since launching REDEMPLO (plozasiran) independently in the U.S. following its approval by the FDA on November 18, 2025, as an adjunct to diet to reduce triglycerides in adults with familial chylomicronemia syndrome (FCS). Key metrics include: Total prescriptions received and in process to date exceeds 400, representing greater than 40% growth over just the last four weeks alone; A total of approximately 180 patients to date have received at least one pre-filled syringe shipment; New weekly prescriptions are accelerating - currently averaging approximately 30 new written prescriptions per week; Approximately 85% of prescriptions were for patients naive to the APOC3 class — a strong signal that physicians are identifying and treating patients with FCS who have never had access to an effective therapy. Patients switching from other APOC3 targeted therapies largely account for the remainder; Updated the U.S. wholesale acquisition cost (WAC) of REDEMPLO to $45,000 per patient per year, representing a premium to the competing APOC3 inhibitor approved for FCS which the company believes is supported by its clinical evidence. This price reflects Arrowhead’s commitment to optimize market access for all patients with FCS. As part of the One-REDEMPLO unified pricing model, the new price is intended to remain consistent across FCS and severe hypertriglyceridemia (SHTG), if that indication is approved, which potentially simplifies payer contracting and eliminates pricing complexity that could complicate future formulary negotiations; Key R&D Events

Following U.S. FDA approval of REDEMPLO in 2025, secured positive regulatory action in four additional geographies for patients with genetically confirmed and clinically diagnosed FCS: The Australian Therapeutic Goods Administration (TGA) approved REDEMPLO (plozasiran), as an adjunct to diet to reduce triglyceride levels for adult patients with familial chylomicronaemia syndrome in Australia; Received positive CHMP opinion recommending approval of REDEMPLO (plozasiran) to reduce triglycerides in adults with familial chylomicronemia syndrome in Europe. The European Commission is expected to issue a decision on REDEMPLO’s Marketing Authorization in the second quarter of 2026; The Chinese National Medical Products Administration (NMPA) approved REDEMPLO (plozasiran) for the reduction of triglyceride levels in adult patients with familial chylomicronemia syndrome. REDEMPLO will be marketed in Greater China by Sanofi under an agreement between Sanofi and Arrowhead; Health Canada issued a Notice of Compliance (NOC) authorizing REDEMPLO (plozasiran) as an adjunct to diet to reduce triglycerides in adults with familial chylomicronemia syndrome for whom standard triglyceride lowering therapies have been inadequate. REDEMPLO is expected to be available later this year in Canada and the company anticipates it will be marketed independently by Arrowhead; Presented new long-term efficacy and safety data for plozasiran across a spectrum of hypertriglyceridemia at the American College of Cardiology’s 75th Annual Scientific Session and Expo. Key highlights include: Patients with severe hypertriglyceridemia achieved an 83% median reduction in triglycerides (TG), with 96% of patients achieving TG levels below 500 mg/dL, a threshold associated with increased risk of acute pancreatitis; No adjudicated acute pancreatitis events occurred in any patient receiving plozasiran during the two-year Phase 2b open-label expansion (OLE) study; Favorable and durable improvements in atherogenic lipoproteins, including remnant cholesterol, non-HDL cholesterol, and ApoB, were observed, with a safety profile consistent with earlier trials; Initiated and dosed the first subjects in a Phase 1/2a clinical trial of ARO-DIMER-PA, the company’s investigational RNA interference (RNAi) therapeutic being developed as a potential treatment for atherosclerotic cardiovascular disease (ASCVD) due to mixed hyperlipidemia: ARO-DIMER-PA is designed to silence expression of the proprotein convertase subtilisin kexin 9 (PCSK9) and apolipoprotein C3 (APOC3) genes. This represents an important step forward for the RNAi field as it is the first dual-functional clinical candidate to target two genes simultaneously in one molecule; Announced interim clinical data on our RNAi-based obesity candidates, ARO-INHBE and ARO-ALK7, showing weight loss in obese patients with diabetes and improved measures of body composition; In obese patients with type 2 diabetes mellitus, ARO-INHBE in combination with tirzepatide achieved -9.4% weight loss at week 16, representing an approximately two-fold improvement versus -4.8% on tirzepatide alone; ARO-INHBE drove robust fat reduction including -23.2% visceral fat, -15.4% total fat, and -76.7% liver fat reduction, representing an approximately three-fold improvement in all three measures versus tirzepatide alone in obese diabetic patients; ARO-ALK7 is the first RNAi-therapeutic to show knockdown in humans of an adipocyte expressed gene, achieving a mean reduction of -88% in ALK7 mRNA with a maximum reduction of -94%; ARO-ALK7 monotherapy achieved a reduction of -14.1% (single dose, week 8) in placebo adjusted visceral fat; Key Corporate Events

Announced, earlier this week, an exclusive worldwide license agreement with Madrigal Pharmaceuticals for ARO-PNPLA3, Arrowhead’s clinical stage RNAi therapeutic designed to reduce liver expression of patatin-like phospholipase domain containing 3 (PNPLA3) as a potential treatment for patients with metabolic dysfunction-associated steatohepatitis (MASH): Under the terms of the agreement, Madrigal will make a $25 million upfront payment to Arrowhead. Arrowhead is also eligible to receive development, regulatory, and sales milestone payments of up to $975 million. Arrowhead is further eligible to receive tiered royalties on commercial sales ranging from high-single digits to the mid-teens; In a Phase 1 single-ascending dose clinical study, ARO-PNPLA3 achieved encouraging results, including a dose-dependent mean reduction in liver fat of up to 40% in patients homozygous for the I148M mutation, no apparent treatment emergent increases in triglycerides or LDL-cholesterol, and a positive safety and tolerability profile at all doses studied; Meaningfully strengthened the balance sheet through two concurrent public offerings with gross proceeds totaling $930 million and consisting of: $700 million of 0.00% convertible senior notes with a 35% conversion premium (initial conversion price of approximately $87.08 per share of common stock) due 2032; $230 million through issuance of shares of common stock, at a public offering price of $64.50 per share (or, in lieu of shares of common stock to certain investors, pre-funded warrants); A capped call transaction to reduce dilution, with the cap price set at $119.33, representing a premium of approximately 85% over the public offering price of $64.50 per share in the common stock offering; Webcast and Conference Call and Details

Investors may access a live audio webcast on the Events and Presentations page under the Investors section of the Arrowhead website. A replay of the webcast will be available approximately two hours after the conclusion of the call.

For analysts that wish to participate in the conference call, please register at https://register-conf.media-server.com/register/BI94a3f6754bd3471e8e895704fb645ee5. Once registered, you will receive the dial-in number and a personalized PIN code that will be required to access the call.

Selected Fiscal 2026 Second Quarter Financial Results 

ARROWHEAD PHARMACEUTICALS, INC.

CONSOLIDATED CONDENSED FINANCIAL INFORMATION

(in thousands, except per share amounts)

  Three months Ended March 31,

OPERATING SUMMARY

2026

2025

Revenue

$

73,737

$

542,709

Operating Expenses:

Research and development

173,253

133,102

General and administrative expenses

41,744

28,405

Total operating expenses

214,997

161,507

Operating (loss) income

(141,260

)

381,202

Total other income (expense)

3,695

(11,586

)

(Loss) income before income tax expense and noncontrolling interest

(137,565

)

369,616

Income tax expense

7

1,753

Net (loss) income including noncontrolling interest

(137,572

)

367,863

Net loss attributable to noncontrolling interest, net of tax

(4,840

)

(2,582

)

Net (loss) income attributable to Arrowhead Pharmaceuticals, Inc.

(132,732

)

370,445

Net (loss) income per share attributable to Arrowhead Pharmaceuticals, Inc. - Diluted

$

(0.93

)

$

2.75

Weighted-average shares used in calculating - Diluted

142,417

134,484

  March 31,

September 30,

2026

2025

FINANCIAL POSITION SUMMARY

(unaudited)

Cash, cash equivalents and restricted cash

$

188,517

$

226,548

Available-for-sale securities, at fair value and short-term investments

1,595,574

692,818

Total cash resources (Cash, cash equivalents and restricted cash and Available-for-sale securities, at fair value and short-term investments)

1,784,091

919,366

Other current and long-term assets

484,174

465,929

Total Assets

$

2,268,265

$

1,385,295

Liability related to the sale of future royalties

$

383,829

$

367,397

Credit Facility

199,639

254,883

Deferred revenue

157,158

2,399

Convertible notes, net

681,940

-

Other liabilities

246,783

257,200

Total Liabilities

$

1,669,349

$

881,879

  Total Arrowhead Pharmaceuticals, Inc. Stockholders' Equity

613,977

466,052

Noncontrolling Interest

(15,061

)

37,364

Total Noncontrolling Interest and Stockholders' Equity

$

598,916

$

503,416

Total Liabilities, Noncontrolling Interest and Stockholders' Equity

$

2,268,265

$

1,385,295

  Shares Outstanding

140,571

135,702

About REDEMPLO® (plozasiran)

REDEMPLO (plozasiran) is approved by the U.S. Food and Drug Administration as an adjunct to diet to reduce triglycerides in adults with Familial Chylomicronemia Syndrome (FCS). REDEMPLO is an siRNA therapeutic designed to suppress the production of apoC-III, a protein produced in the liver that raises triglyceride levels by slowing their breakdown and clearance. By targeting apoC-III with sustained silencing, REDEMPLO delivers significant reductions in triglyceride levels. REDEMPLO is the first and only siRNA FDA-approved treatment studied in both genetically confirmed and clinically diagnosed patients living with FCS.

For more information about REDEMPLO, visit Our Medicines.

IMPORTANT SAFETY INFORMATION

CONTRAINDICATIONS

None.

ADVERSE REACTIONS

Most common adverse reactions in REDEMPLO treated patients (incidence ≥10% of patients treated with REDEMPLO and >5% more frequently than with placebo) are hyperglycemia, headache, nausea, and injection site reaction.

Please see full U.S. Prescribing Information for REDEMPLO®.

About Arrowhead Pharmaceuticals

Arrowhead Pharmaceuticals (NASDAQ: ARWR) is a commercial-stage pharmaceutical company developing medicines that treat intractable diseases by silencing the genes that cause them, harnessing the natural RNA interference (RNAi) mechanism. The company has built a broad portfolio of clinical and commercial RNAi therapeutics through its industry-leading targeted RNAi molecule (TRiM™) platform, which can precisely silence genes in a wide range of cell types, including liver, lung, muscle, adipose, and central nervous system tissue. At Arrowhead, we rapidly advance potential best- and first-in-class RNAi treatments for diseases with significant unmet medical need, because every day matters to the patients we serve.

For more information, please visit www.arrowheadpharma.com, or follow us on X (formerly Twitter) at @ArrowheadPharma, LinkedIn, Facebook, and Instagram. To be added to the Company's email list and receive news directly, please visit http://ir.arrowheadpharma.com/email-alerts.

Safe Harbor Statement under the Private Securities Litigation Reform Act:

This news release contains forward-looking statements within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. Any statements contained in this release except for historical information may be deemed to be forward-looking statements. Without limiting the generality of the foregoing, words such as “may,” “will,” “expect,” “believe,” “anticipate,” “hope,” “intend,” “plan,” “project,” “could,” “estimate,” “continue,” “target,” “forecast” or “continue” or the negative of these words or other variations thereof or comparable terminology are intended to identify such forward-looking statements. In addition, any statements that refer to projections of our future financial performance, trends in our business, expectations for our product pipeline, products or product candidate or other characterizations of future events or circumstances are forward-looking statements. These forward-looking statements include, but are not limited to, statements about our beliefs and expectations regarding the long-term impacts of REDEMPLO® (plozasiran) on patient health and the health care system; our beliefs and expectations regarding the pricing, value, or expected timing for availability of our drugs and drug candidates; and our believes and expectations around the potential uses and value of the TRiM™ platform. These statements are based upon our current expectations and speak only as of the date hereof. Actual results or outcomes may differ materially and adversely from those expressed in any forward-looking statements as a result of numerous factors and uncertainties the safety and efficacy of our products and product candidates, pricing and reimbursement decisions related to our products, demand for our products, decisions of regulatory authorities and the timing thereof, the duration and impact of regulatory delays in our clinical programs, our ability to finance our operations, the likelihood and timing of the receipt of future milestone and licensing fees, the future success of our scientific studies, the timing for starting and completing clinical trials, rapid technological change in our markets, the enforcement of our intellectual property rights, and the other risks and uncertainties described in our most recent Annual Report on Form 10-K, subsequent Quarterly Reports on Form 10-Q and other documents filed with the Securities and Exchange Commission from time to time. We assume no obligation to update or revise forward-looking statements to reflect new events or circumstances.

Source: Arrowhead Pharmaceuticals, Inc.

More News From Arrowhead Pharmaceuticals, Inc.

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2026-06-12 16:37 1mo ago
2026-05-07 23:11 2mo ago
Arrowhead Pharmaceuticals, Inc. (ARWR) Q2 2026 Earnings Call Transcript
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Arrowhead Pharmaceuticals, Inc. (ARWR) Q2 2026 Earnings Call Transcript
2026-06-12 16:37 1mo ago
2026-05-12 15:20 2mo ago
Arrowhead Pharmaceuticals: A True Inflection Point Has Arrived
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Arrowhead Pharmaceuticals presents a compelling bull case with a strong pipeline and a new commercialization status thanks to REDEMPLO FDA approval. ARWR's cardiometabolic pipeline, including REDEMPLO's potential updating and ARO-DIMER-PA's dual-target RNAi, supports future growth and market reach. The CNS drug ARO-MAPT that targets tauopathies linked to diseases like Alzheimer's will produce Phase 1 data in 2H 2026. This could drive a positive valuation rerating for ARWR.
2026-06-12 16:37 1mo ago
2026-05-14 05:09 2mo ago
Arrowhead Pharmaceuticals Eyes $4B REDEMPLO Opportunity as RNAi Pipeline Readouts Near
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Want Diversified Upside in Biotechnology? Check out LABUArrowhead Pharmaceuticals NASDAQ: ARWR is moving into a more commercial phase while continuing to expand its RNA interference pipeline, Chief Executive Officer Chris Anzalone said during a presentation with BofA pharma and biotech analyst Jason Gerberry at the BofA Annual Healthcare Conference.

Anzalone described Arrowhead as an “and” company rather than an “or” company, saying the company intends to build its commercial capabilities without slowing its research operations. He said Arrowhead can now address seven different cell types, with five currently in clinical studies, and remains focused on RNAi innovation.

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The company also expects several pipeline readouts later this year, including initial data from its dimer, or bispecific, platform and from its CNS platform.

REDEMPLO Launch Off to a Faster-Than-Expected Start A major focus of the discussion was REDEMPLO, Arrowhead’s commercial launch in familial chylomicronemia syndrome, or FCS. Anzalone said the launch “has gone well so far,” noting that Arrowhead had recorded more than 400 prescriptions after one full quarter of sales. He said adoption has been “a bit more rapid” than the company expected.

Anzalone emphasized that FCS remains an education market. While some patients with genetic FCS are diagnosed, he said Arrowhead believes that group represents a small portion of the broader FCS population. The company is also focused on patients with clinical FCS, who do not have known genetic mutations associated with traditional FCS but still have very high triglycerides and a substantially increased risk of pancreatitis.

He said many patients currently categorized as having severe hypertriglyceridemia, or sHTG, may be more appropriately diagnosed as having clinical FCS. That overlap, he said, is informing Arrowhead’s approach as it looks toward a broader sHTG opportunity.

SHASTA Data Expected in Third Quarter Arrowhead is awaiting pivotal data from the SHASTA-3 and SHASTA-4 studies in sHTG, with topline results expected after last patient, last visit near the end of June and subsequent database lock and analysis. Anzalone said the primary endpoint is triglyceride lowering and expressed confidence based on prior experience.

“This essentially works in 100% of people,” Anzalone said, referring to triglyceride reduction in the company’s FCS phase 3 study, where he said there were no non-responders. He contrasted that with what he described as about 20% non-responders for a competitor’s product.

The company is also watching whether the studies show a reduction in acute pancreatitis, a key secondary endpoint. Anzalone said Arrowhead was encouraged by pancreatitis data from competitor Ionis and is “cautiously optimistic” that SHASTA-3 and SHASTA-4 may show a benefit. However, he noted that the event numbers are relatively small and that “funny things can happen with small numbers.”

Arrowhead also has SHASTA-5, an ongoing event-driven study designed to show an improvement in pancreatitis. Anzalone said if SHASTA-3 and SHASTA-4 show a pancreatitis benefit, Arrowhead could decide to stop SHASTA-5, but no decision has been made. He said the timing for SHASTA-5 is difficult to predict because it is event-driven.

Anzalone said pancreatitis data would not be gating for U.S. payers, in Arrowhead’s view, but could matter more outside the United States, where some geographies may require acute pancreatitis data on the label for reimbursement.

Pricing and Market Opportunity Gerberry asked about pricing dynamics in a two-player APOC3-modulating market that includes Ionis’ TRYNGOLZA. Anzalone said Arrowhead does not expect to aggressively discount REDEMPLO and views the product less as a triglyceride-lowering drug and more as a pancreatitis drug.

He said Arrowhead is comfortable with a list price at a slight premium to TRYNGOLZA, citing quarterly dosing, safety profile and historical triglyceride reduction. Anzalone said he believes the sHTG market can support two competitors and that having two companies educating physicians and payers may help the category develop more rapidly.

Asked about peak U.S. sales potential, Anzalone said he would be “a bit more aggressive” than a $3 billion peak estimate referenced by Gerberry, saying he sees a potential $3 billion to $4 billion peak for REDEMPLO. However, he cautioned that the market will take time to develop because of the need for physician education.

Obesity and Cardiometabolic Pipeline Arrowhead also discussed ARO-INHBE, an obesity-related program the company is studying in combination with GLP-1 therapies. Anzalone said Arrowhead has long viewed INHBE as a potential combination therapy rather than a monotherapy.

He said early data in an obese diabetic population showed a doubling of fat reduction and a tripling of liver fat reduction, which he called “eye-opening.” Arrowhead is designing phase 2 studies and expects to begin them this year, with plans to study INHBE as a potential MASH therapy and obesity therapy.

Anzalone also highlighted ARO-ALK7, which targets the Activin E/ALK-7 axis. He said Arrowhead expects more data in the second half of this year and is interested in safety, target knockdown, potential weight loss effects and fat distribution. He said successful adipose delivery in humans could open additional targets and potential dimer approaches.

Arrowhead also expects data from its PCSK9/APOC3 dimer in the third quarter. Anzalone said the company believes the program could address roughly 20 million people in the U.S. with mixed hyperlipidemia.

CNS Platform and Capital Position Anzalone said Arrowhead expects initial data from ARO-MAPT, its first subcutaneously administered CNS drug, later this year. The initial readout will be in healthy volunteers and will focus on whether animal results translate to humans, including tau knockdown and tolerability.

If the readout is positive, Anzalone said Arrowhead could move quickly into additional CNS programs, with multiple candidates potentially entering clinical studies in 2027 and possibly one by late 2026.

On partnering, Anzalone said Arrowhead reported about $1.8 billion in cash on its most recent quarterly update and is positioned to advance its current programs itself. He said the company currently has no interest in partnering plozasiran, zodasiran or the PCSK9/APOC3 dimer, though he acknowledged that partnership views could change in the future.

About Arrowhead Pharmaceuticals NASDAQ: ARWRArrowhead Pharmaceuticals, Inc is a clinical-stage biopharmaceutical company focused on the discovery, development and commercialization of RNA interference (RNAi) therapeutics. Since its founding in 2008, Arrowhead has leveraged its proprietary delivery platform—known internally as the Advanced RNAi Compound (ARC) technology—to silence disease-causing genes in patients suffering from genetically defined diseases. The company's approach aims to offer durable, targeted treatments across a range of therapeutic areas.

The company's pipeline includes multiple candidates in various stages of development.

This instant news alert was generated by narrative science technology and financial data from MarketBeat in order to provide readers with the fastest reporting and unbiased coverage. Please send any questions or comments about this story to [email protected].

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2026-06-12 16:37 1mo ago
2026-05-14 21:50 2mo ago
Arrowhead Pharmaceuticals, Inc. (ARWR) Presents at Bank of America Global Healthcare Conference 2026 Transcript
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Arrowhead Pharmaceuticals, Inc. (ARWR) Presents at Bank of America Global Healthcare Conference 2026 Transcript
2026-06-12 16:37 1mo ago
2026-05-20 10:08 2mo ago
Arrowhead Pharmaceuticals Eyes Q3 SHASTA Data as REDEMPLO Approvals Build Momentum
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Want Diversified Upside in Biotechnology? Check out LABUArrowhead Pharmaceuticals NASDAQ: ARWR executives said the company is entering a key period marked by new regulatory approvals, early commercial progress for REDEMPLO and upcoming Phase 3 data in severe hypertriglyceridemia, during a fireside chat at RBC Capital Markets’ 2026 Global Healthcare Conference.

Vince Anzalone, Arrowhead’s vice president of investor relations, said the company is “on the most solid footing” in its history, citing regulatory progress for REDEMPLO and a strengthened balance sheet. He said the product, approved by the U.S. Food and Drug Administration in November of last year, has since received approval in China, Australia and Canada, as well as a positive CHMP opinion in Europe. Arrowhead expects European Commission approval shortly, he said.

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Anzalone also pointed to the company’s first full quarter of commercial sales for REDEMPLO, which he characterized as encouraging. He said dynamics in the market for FCS, the rare portion of severe hypertriglyceridemia, are favorable for both Arrowhead and its competitor.

SHASTA-3 and SHASTA-4 Readout Expected in Q3 The most closely watched near-term catalyst discussed at the conference was the expected readout from SHASTA-3 and SHASTA-4, Phase 3 studies evaluating Arrowhead’s therapy in severe hypertriglyceridemia. Anzalone said the company expects to complete the studies toward the end of June, with data expected in the third quarter.

James Hamilton, Arrowhead’s chief medical officer, said the company remains “cautiously optimistic” that the studies will show statistical significance on acute pancreatitis. He said Arrowhead is confident the studies will be sufficiently powered based on blinded event rates.

Hamilton also discussed a change in how acute pancreatitis events are adjudicated. Arrowhead moved from the strict Atlanta criteria used in the PALISADE study to a modified approach that includes definite, probable and possible acute pancreatitis events. He said the change was made before any acute pancreatitis events were adjudicated and does not alter the statistical analysis.

The modified scale, Hamilton said, has been accepted by regulators in the U.S. and Europe, key opinion leaders and major journals. He added that it is the same scale used by Arrowhead’s competitor, which may allow for more direct comparison.

Anzalone said that after the last patient’s last visit, Arrowhead will need to lock the database and conduct the analysis, a process he described as typically taking four to eight weeks.

SHASTA-5 Positioned as Additional Support Arrowhead also discussed SHASTA-5, a study designed specifically to evaluate acute pancreatitis events as the primary endpoint in high-risk patients. Hamilton described the trial as a “belt and suspenders” approach that could help with payers, particularly because it is focused on acute pancreatitis.

Hamilton said enrollment has picked up after the company broadened entry criteria. Initially, patients needed stricter triglyceride and acute pancreatitis history requirements. The revised criteria include at least one acute pancreatitis event within the past five years, a history of triglycerides above 880 and screening triglycerides above 500. Hamilton said the broader criteria should help identify more eligible patients without losing the ability to capture events.

Hamilton said data from SHASTA-5 could arrive in late 2027 or early 2028, though he cautioned that timing is difficult to predict because the trial is event-driven. Anzalone emphasized that SHASTA-5 is not required for submission for approval in severe hypertriglyceridemia, either in the U.S. or abroad.

Safety Signals and Commercial Opportunity Executives addressed investor questions about liver fat and hemoglobin A1c signals seen in the broader APOC3 drug class. Hamilton said Arrowhead has not yet seen unblinded liver fat data from SHASTA-3 and SHASTA-4. He said the company’s hypothesis is that liver fat increases observed by a competitor may be more related to the competitor’s antisense oligonucleotide than to the target itself, though he did not rule out an on-target mechanism.

Hamilton said Arrowhead did not see an increase in liver fat at the 25-milligram dose being used as the go-to-market dose in pivotal studies. At a 50-milligram dose in an earlier study, he said there was about a 2% absolute increase in liver fat. Anzalone said the 25-milligram dose was selected because it appeared maximally active, not due to safety concerns.

On hemoglobin A1c, Hamilton said the company has seen an approximately 0.25% absolute increase, mostly in patients who were diabetic at baseline. He said the issue is generally manageable through adjustments to diabetes medications.

Anzalone said Arrowhead continues to view REDEMPLO as a $3 billion to $4 billion peak revenue opportunity. He said discussions with physicians and payers have reinforced the company’s belief that the APOC3 class is viewed as valuable, adding that some sell-side analysts now estimate the overall class could reach $9 billion to $10 billion annually.

Pipeline Focus Remains Cardiometabolic Beyond REDEMPLO, Anzalone said Arrowhead has about $1.8 billion in cash and is positioned to support a broad development agenda. He highlighted zodasiran as the company’s hoped-for second approved product and said Arrowhead expects a readout later this year for a dual-function molecule designed to silence PCSK9 and APOC3 for mixed hyperlipidemia.

Hamilton also discussed Arrowhead’s ARO-INHBE program, noting that monotherapy weight loss has been modest, while reductions in liver fat and visceral fat have been more notable. He said the strongest weight-loss signal appeared in combination with tirzepatide in patients with type 2 diabetes, a group that can be harder to treat with GLP-1 therapies alone. Hamilton said Arrowhead is still evaluating regulatory endpoints for combination therapy in weight loss, including whether visceral fat reduction could support a path forward.

Asked about Biogen’s recent tau data, Hamilton said the results were generally supportive of the tau hypothesis, particularly because Biogen is moving the molecule into Phase 3. He said Arrowhead’s own approach uses siRNA-mediated knockdown and subcutaneous dosing rather than intrathecal administration, which he described as a potential advantage.

Anzalone said Arrowhead’s capital allocation will be increasingly weighted toward cardiometabolic programs, while the company may be more aggressive in partnering non-core assets. He said the company has more than 20 drugs in clinical studies and recently completed a deal with Madrigal on a MASH asset targeting PNPLA3.

About Arrowhead Pharmaceuticals NASDAQ: ARWRArrowhead Pharmaceuticals, Inc is a clinical-stage biopharmaceutical company focused on the discovery, development and commercialization of RNA interference (RNAi) therapeutics. Since its founding in 2008, Arrowhead has leveraged its proprietary delivery platform—known internally as the Advanced RNAi Compound (ARC) technology—to silence disease-causing genes in patients suffering from genetically defined diseases. The company's approach aims to offer durable, targeted treatments across a range of therapeutic areas.

The company's pipeline includes multiple candidates in various stages of development.

This instant news alert was generated by narrative science technology and financial data from MarketBeat in order to provide readers with the fastest reporting and unbiased coverage. Please send any questions or comments about this story to [email protected].

Should You Invest $1,000 in Arrowhead Pharmaceuticals Right Now?Before you consider Arrowhead Pharmaceuticals, you'll want to hear this.

MarketBeat keeps track of Wall Street's top-rated and best performing research analysts and the stocks they recommend to their clients on a daily basis. MarketBeat has identified the five stocks that top analysts are quietly whispering to their clients to buy now before the broader market catches on... and Arrowhead Pharmaceuticals wasn't on the list.

While Arrowhead Pharmaceuticals currently has a Moderate Buy rating among analysts, top-rated analysts believe these five stocks are better buys.

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2026-06-12 16:37 1mo ago
2026-05-26 10:00 2mo ago
Arrowhead Pharmaceuticals Presents New Positive Clinical Cardiometabolic Data at the 94th European Atherosclerosis Society (EAS) Congress
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FMP Stock News
Original source text
[url="]Arrowhead Pharmaceuticals, Inc.[/url] (NASDAQ: ARWR) today presented new positive clinical data for plozasiran supporting its use in patients with moder
2026-06-12 16:37 1mo ago
2026-05-26 10:00 2mo ago
Arrowhead Pharmaceuticals Presents New Positive Clinical Cardiometabolic Data at the 94th European Atherosclerosis Society (EAS) Congress
ARWR Arrowhead Pharmaceuticals
FMP Stock News
Original source text
-

- New data support potential use of plozasiran without dose adjustment in patients with moderate-to-severe renal or moderate hepatic impairment

- Case report suggests that preconception exposure to plozasiran may be associated with sustained lowering of fasting triglyceride levels throughout the term of a pregnancy

PASADENA, Calif.--(BUSINESS WIRE)--Arrowhead Pharmaceuticals, Inc. (NASDAQ: ARWR) today presented new positive clinical data for plozasiran supporting its use in patients with moderate-to-severe renal impairment or moderate hepatic impairment without the need for dose adjustment, and a case report suggesting that preconception exposure to plozasiran may be associated with sustained lowering of fasting triglyceride (TG) levels through the term of a pregnancy. The data were presented in two oral presentations at the 94th European Atherosclerosis Society (EAS) Congress, taking place in Athens, Greece from May 24-27.

Patients living with extremely high triglycerides often suffer from significant comorbidities. Today’s data represent an important step in bridging the gap between patient needs and scientific innovation.

Share “Patients living with extremely high triglycerides often suffer from significant comorbidities. Today’s data represent an important step in bridging the gap between patient needs and scientific innovation,” said Jennifer Hellawell, MD, board-certified cardiologist and Vice President of Clinical Development at Arrowhead Pharmaceuticals. “As a physician at heart, I’m proud to be part of the team advancing next-generation therapies for this underserved community. We’re excited to have better characterized the PK and PD of plozasiran in this potentially broader patient population. These data bring us closer to delivering meaningful impact for patients.”

Plozasiran is a small interfering RNA (siRNA) medicine designed to reduce hepatic production of apolipoprotein C‑III (APOC3) through targeted RNA interference. It received regulatory approval in the United States, China, Australia, and Canada as an adjunct to diet to reduce triglycerides in adults with familial chylomicronemia syndrome (FCS) and is currently being investigated in patients with severe hypertriglyceridemia (sHTG). Patients with FCS and sHTG often present with hepatic steatosis or renal impairment. Because the safety and tolerability of plozasiran in the setting of hepatic and/or renal impairment remains unknown, this study assessed the impact of hepatic or renal impairment on the pharmacokinetics, pharmacodynamics, and safety of a single 25 mg dose of plozasiran.

Despite modest increases in plozasiran exposure, PD responses (APOC3 and TG reduction) were similar between control cohorts and those with moderate-to-severe renal or moderate hepatic impairment. In addition, plozasiran was generally safe and well-tolerated, with no new safety signals identified. Together, these data support the use of 25 mg plozasiran in patients with moderate-to-severe renal impairment or moderate hepatic impairment without dose adjustment. Future trials are needed to help further evaluate plozasiran safety in patients with advanced liver or renal disease.

In an additional oral presentation, the company highlighted a patient case report that suggests that preconception exposure to plozasiran may be associated with sustained lowering of fasting TG levels throughout the term of a pregnancy, representing the second case report published on FCS patients in the PALISADE study who discontinued use of plozasiran prior to conception and achieved successful pregnancies. While additional data are needed to define the safety and efficacy of APOC3–targeted therapies during pregnancy, these findings are consistent with the prolonged pharmacodynamic effects of APOC3 inhibition reported in previous PALISADE studies.

Presentation Details:

Session Title: Late Breaking Clinical Abstracts
Title: Pharmacokinetics, Pharmacodynamics, and Safety of Plozasiran in Subjects with Renal or Hepatic Impairment
Date & Time: Tuesday, May 26th, 3:45 - 5:15PM EEST
Presenting Author: Jennifer Hellawell, MD

Session Title: EAS Stage, Outreach and Case Presentations
Title: A Case Report of a Pregnant Woman with Familial Chylomicronemia Syndrome Treated with Plozasiran, a Small Interfering RNA Against APOC3
Date & Time: Tuesday, May 26th, 8:30 - 10:30AM EEST
Presenting Author: Ann Mertens, MD

Today’s presentations will be made available on the EAS Conference website and on the Events and Presentations page under the Investors section of the Arrowhead website.

About REDEMPLO® (plozasiran)

REDEMPLO (plozasiran) is the first and only siRNA treatment approved in these countries that has been studied in both genetically confirmed and clinically diagnosed patients living with FCS. REDEMPLO is a first-in-class siRNA therapeutic designed to suppress the production of apoC-III, a protein produced in the liver that raises triglyceride levels by slowing their breakdown and clearance. By targeting apoC-III with sustained silencing, REDEMPLO delivers significant reductions in triglyceride levels. REDEMPLO is self-administered via subcutaneous injection once every three months.

The EMA CHMP has adopted a positive opinion recommending the European Marketing Authorization of REDEMPLO (plozasiran), which is already approved by the U.S. Food and Drug Administration, Health Canada, the Australian Therapeutic Goods Administration, and China’s National Medical Products Administration as an adjunct to diet to reduce triglycerides for adults with Familial Chylomicronemia Syndrome (FCS).

Plozasiran is also being investigated in the SHASTA-3 (NCT06347003), SHASTA-4 (NCT06347016), and SHASTA-5 (NCT06880770) Phase 3 studies in adults with severe hypertriglyceridemia and the MUIR-3 (NCT06347133) Phase 3 study in adults with hypertriglyceridemia. In December 2025, plozasiran was granted Breakthrough Therapy designation by the U.S. FDA in severe hypertriglyceridemia.

For more information about REDEMPLO, visit Our Medicines.

About Arrowhead Pharmaceuticals

Arrowhead Pharmaceuticals (NASDAQ: ARWR) is a commercial-stage pharmaceutical company developing medicines that treat intractable diseases by silencing the genes that cause them, harnessing the natural RNA interference (RNAi) mechanism. The company has built a broad portfolio of clinical and commercial RNAi therapeutics through its industry-leading targeted RNAi molecule (TRiM™) platform, which can precisely silence genes in a wide range of cell types, including liver, lung, muscle, adipose, and central nervous system tissue. At Arrowhead, we rapidly advance potential best- and first-in-class RNAi treatments for diseases with significant unmet medical need, because every day matters to the patients we serve.

For more information, please visit www.arrowheadpharma.com, or follow us on X (formerly Twitter) at @ArrowheadPharma, LinkedIn, Facebook, and Instagram. To be added to the Company's email list and receive news directly, please visit http://ir.arrowheadpharma.com/email-alerts.

Safe Harbor Statement under the Private Securities Litigation Reform Act:

This news release contains forward-looking statements within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. Any statements contained in this release except for historical information may be deemed to be forward-looking statements. Without limiting the generality of the foregoing, words such as “may,” “will,” “expect,” “believe,” “anticipate,” “hope,” “intend,” “plan,” “project,” “could,” “estimate,” “continue,” “target,” “forecast” or “continue” or the negative of these words or other variations thereof or comparable terminology are intended to identify such forward-looking statements. In addition, any statements that refer to projections of our future financial performance, trends in our business, expectations for our product pipeline, products or product candidate or other characterizations of future events or circumstances are forward-looking statements. These forward-looking statements include, but are not limited to, statements about our beliefs and expectations regarding the long-term impacts of REDEMPLO® (plozasiran) on patient health and the health care system; our beliefs and expectations regarding the pricing, value, or expected timing for availability of our drugs and drug candidates; and our believes and expectations around the potential uses and value of the TRiM™ platform. These statements are based upon our current expectations and speak only as of the date hereof. Actual results or outcomes may differ materially and adversely from those expressed in any forward-looking statements as a result of numerous factors and uncertainties the safety and efficacy of our products and product candidates, pricing and reimbursement decisions related to our products, demand for our products, decisions of regulatory authorities and the timing thereof, the duration and impact of regulatory delays in our clinical programs, our ability to finance our operations, the likelihood and timing of the receipt of future milestone and licensing fees, the future success of our scientific studies, the timing for starting and completing clinical trials, rapid technological change in our markets, the enforcement of our intellectual property rights, and the other risks and uncertainties described in our most recent Annual Report on Form 10-K, subsequent Quarterly Reports on Form 10-Q and other documents filed with the Securities and Exchange Commission from time to time. We assume no obligation to update or revise forward-looking statements to reflect new events or circumstances.

Source: Arrowhead Pharmaceuticals, Inc.

More News From Arrowhead Pharmaceuticals, Inc.

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2026-06-12 16:36 1mo ago
2026-05-27 07:00 2mo ago
Arrowhead Pharmaceuticals Presents New Clinical Data on RNAi-based Obesity and MASH Candidate ARO-INHBE at EASL 2026
ARWR Arrowhead Pharmaceuticals
FMP Stock News
Original source text
-

- Targeting Activin E may represent a novel therapeutic strategy for metabolic dysfunction-associated steatohepatitis (MASH) and obesity‑related metabolic dysfunction

- ARO-INHBE produced meaningful reductions in liver fat content as a monotherapy or in combination with low-dose tirzepatide in individuals with obesity with or without Type 2 Diabetes Mellitus (T2DM)

- Longer exposure to ARO-INHBE silencing resulted in continued improvements in visceral fat and liver fat from Week 12 to Week 24

PASADENA, Calif.--(BUSINESS WIRE)--Arrowhead Pharmaceuticals, Inc. (NASDAQ: ARWR) today presented interim results from a Phase 1/2a clinical trial of ARO-INHBE, the company’s investigational RNA interference (RNAi) therapeutic being developed as a potential treatment for obesity and metabolic dysfunction-associated steatohepatitis (MASH). The data presented at the European Association for the Study of the Liver Congress (EASL 2026) demonstrate that ARO-INHBE treatment led to clinically meaningful reductions in liver fat as a monotherapy and in combination with low-dose tirzepatide, a GLP-1/GIP receptor co-agonist, in adults with obesity. Arrowhead is currently engaging with regulatory authorities on additional designs and endpoints for potential Phase 2 studies in MASH and obesity.

We believe that targeting the Activin E/ALK7 pathway, a genetically validated pathway that regulates adipose fat storage, is a promising strategy to address MASH and obesity‑related metabolic dysfunction.

Share “Building on prior interim results from a Phase 1/2a study of ARO-INHBE, which showed encouraging signals on weight loss and improved measures of body composition in obese patients with diabetes, today we presented additional results at the EASL 2026 congress. These data provide encouraging signals on the safety, activity, and efficacy of ARO-INHBE, particularly with respect to liver fat reductions as a monotherapy or in combination with low-dose tirzepatide in patients with or without Type 2 Diabetes Mellitus,” said James Hamilton, M.D., MBA, Chief Medical Officer and Head of R&D at Arrowhead. “We believe that targeting the Activin E/ALK7 pathway, a genetically validated pathway that regulates adipose fat storage, is a promising strategy to address MASH and obesity‑related metabolic dysfunction and may complement existing incretin-based approaches in the treatment of obesity.”

The EASL 2026 poster may be accessed on the Events and Presentations page on the Investors section of the Arrowhead website.

Select ARO-INHBE Phase 1/2a Results

In participants with obesity, dose-dependent reductions in Activin E were observed following a single administration of ARO-INHBE, with a mean maximum reduction of 85.3% achieved with ARO-INHBE 400 mg and persistent effect beyond 3 months Similar Activin E reductions were observed in participants with obesity and T2DM receiving two doses of ARO-INHBE (200 mg or 400 mg) in combination with tirzepatide 5 mg, demonstrating persistent effect through Week 24 with the potential for infrequent twice per year dose administration Participants with obesity and baseline liver fat content (LFC) greater than 8% receiving 200mg or greater of ARO-INHBE monotherapy (n=10; baseline LFC 14.5±5.1%) had a placebo-adjusted post-dose LFC reduction of 44% (t-test: p < 0.01) ARO-INHBE in combination with low-dose tirzepatide (5 mg) resulted in enhanced reductions in visceral adipose tissue and LFC compared to tirzepatide alone in participants with obesity with or without T2DM Longer exposure to ARO-INHBE resulted in continued improvements in visceral fat and LFC from Week 12 to Week 24 Safety and Tolerability

ARO-INHBE has been generally well tolerated to date as a monotherapy and in combination with tirzepatide in participants with obesity with and without type 2 diabetes. Most treatment emergent adverse events (TEAE) were mild in severity. No TEAEs led to study or study drug discontinuation. Injection site reactions were generally mild and self-limited.

About ARO-INHBE

ARO-INHBE is designed to reduce the hepatic expression of the INHBE gene and its secreted gene product, Activin E. INHBE is a promising genetically validated target in which loss-of-function INHBE variants in humans are associated with improved fat distribution and lower risk of metabolic diseases, such as type 2 diabetes. Activin E acts as a ligand in a pathway that regulates energy homeostasis in adipose tissue. Inhibiting this pathway with investigational ARO-INHBE treatment has the potential to increase lipolysis, and reduce adipose hypertrophy and dysfunction, visceral adiposity, and insulin resistance.

About the AROINHBE-1001 Phase 1/2 Study

AROINHBE-1001 (NCT06700538) is a Phase 1/2a dose-escalating study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of ARO-INHBE in up to 78 adult volunteers with obesity. Part 1 of the study is designed to assess single and multiple doses of ARO-INHBE monotherapy, and Part 2 of the study is designed to assess ARO-INHBE in combination with tirzepatide, a subcutaneously administered GLP-1/GIP receptor co-agonist that has been approved in the United States and the European Union for management of type 2 diabetes mellitus since 2022 and weight management since 2023/2024 respectively.

About Arrowhead Pharmaceuticals

Arrowhead Pharmaceuticals (NASDAQ: ARWR) is a commercial-stage pharmaceutical company developing medicines that treat intractable diseases by silencing the genes that cause them, harnessing the natural RNA interference (RNAi) mechanism. The company has built a broad portfolio of clinical and commercial RNAi therapeutics through its industry-leading targeted RNAi molecule (TRiM™) platform, which can precisely silence genes in a wide range of cell types, including liver, lung, muscle, adipose, and central nervous system tissue. At Arrowhead, we rapidly advance potential best- and first-in-class RNAi treatments for diseases with significant unmet medical need, because every day matters to the patients we serve.

For more information, please visit www.arrowheadpharma.com, or follow us on X (formerly Twitter) at @ArrowheadPharma, LinkedIn, Facebook, and Instagram. To be added to the Company's email list and receive news directly, please visit http://ir.arrowheadpharma.com/email-alerts.

Safe Harbor Statement under the Private Securities Litigation Reform Act:

This news release contains forward-looking statements within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. Any statements contained in this release except for historical information may be deemed to be forward-looking statements. Without limiting the generality of the foregoing, words such as “may,” “will,” “expect,” “believe,” “anticipate,” “hope,” “intend,” “plan,” “project,” “could,” “estimate,” “continue,” “target,” “forecast” or “continue” or the negative of these words or other variations thereof or comparable terminology are intended to identify such forward-looking statements. In addition, any statements that refer to projections of our future financial performance, trends in our business, expectations for our product pipeline, products or product candidate or other characterizations of future events or circumstances are forward-looking statements. These statements are based upon our current expectations and speak only as of the date hereof. Actual results or outcomes may differ materially and adversely from those expressed in any forward-looking statements as a result of numerous factors and uncertainties the safety and efficacy of our products and product candidates, pricing and reimbursement decisions related to our products, demand for our products, decisions of regulatory authorities and the timing thereof, the duration and impact of regulatory delays in our clinical programs, our ability to finance our operations, the likelihood and timing of the receipt of future milestone and licensing fees, the future success of our scientific studies, the timing for starting and completing clinical trials, rapid technological change in our markets, the enforcement of our intellectual property rights, and the other risks and uncertainties described in our most recent Annual Report on Form 10-K, subsequent Quarterly Reports on Form 10-Q and other documents filed with the Securities and Exchange Commission from time to time. We assume no obligation to update or revise forward-looking statements to reflect new events or circumstances.

Source: Arrowhead Pharmaceuticals, Inc.

More News From Arrowhead Pharmaceuticals, Inc.

Back to Newsroom
2026-06-12 16:36 1mo ago
2026-05-27 08:00 2mo ago
Arrowhead Pharmaceuticals Presents New Clinical Data on RNAi-based Obesity and MASH Candidate ARO-INHBE at EASL 2026
ARWR Arrowhead Pharmaceuticals
FMP Stock News
Original source text
[url="]Arrowhead Pharmaceuticals, Inc.[/url] (NASDAQ: ARWR) today presented interim results from a Phase 1/2a clinical trial of ARO-INHBE, the company's invest
2026-06-12 16:36 1mo ago
2026-06-02 07:30 1mo ago
Arrowhead Pharmaceuticals to Participate in Upcoming June 2026 Events
ARWR Arrowhead Pharmaceuticals
FMP Stock News
Original source text
PASADENA, Calif.--(BUSINESS WIRE)--Arrowhead Pharmaceuticals, Inc. (NASDAQ: ARWR) today announced that it is scheduled to participate in the following upcoming events:

2026 Jefferies Global Healthcare Conference – June 2-4, 2026

Type: Fireside Chat Presentation
Date/Time: June 3, 2026, 8:10 am EDT

Goldman Sachs 47th Annual Global Healthcare Conference – June 8-10, 2026

Type: Fireside Chat Presentation
Date/Time: June 10, 2026, 9:00 am EDT

Presentation materials and webcast links, if applicable, may be accessed on the Events and Presentations page under the Investors section of the Arrowhead website.

About Arrowhead Pharmaceuticals

Arrowhead Pharmaceuticals (NASDAQ: ARWR) is a commercial-stage pharmaceutical company developing medicines that treat intractable diseases by silencing the genes that cause them, harnessing the natural RNA interference (RNAi) mechanism. The company has built a broad portfolio of clinical and commercial RNAi therapeutics through its industry-leading targeted RNAi molecule (TRiM™) platform, which can precisely silence genes in a wide range of cell types, including liver, lung, muscle, adipose, and central nervous system tissue. At Arrowhead, we rapidly advance potential best- and first-in-class RNAi treatments for diseases with significant unmet medical need, because every day matters to the patients we serve.

For more information, please visit arrowheadpharma.com, or follow us on X (formerly Twitter) at @ArrowheadPharma, LinkedIn, Facebook, and Instagram. To be added to the Company’s email list and receive news directly, please visit ir.arrowheadpharma.com/email-alerts.

Safe Harbor Statement under the Private Securities Litigation Reform Act:

This news release contains forward-looking statements within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. Any statements contained in this release except for historical information may be deemed to be forward-looking statements. Without limiting the generality of the foregoing, words such as “may,” “will,” “expect,” “believe,” “anticipate,” “hope,” “intend,” “plan,” “project,” “could,” “estimate,” “continue,” “target,” “forecast” or “continue” or the negative of these words or other variations thereof or comparable terminology are intended to identify such forward-looking statements. In addition, any statements that refer to projections of our future financial performance, trends in our business, expectations for our product pipeline or product candidates, including anticipated regulatory submissions and clinical program results, prospects or benefits of our collaborations with other companies, or other characterizations of future events or circumstances are forward-looking statements. These forward-looking statements include, but are not limited to, statements about the initiation, timing, progress and results of our preclinical studies and clinical trials, and our research and development programs; our expectations regarding the potential benefits of the partnership, licensing and/or collaboration arrangements and other strategic arrangements and transactions we have entered into or may enter into in the future; our beliefs and expectations regarding milestone, royalty or other payments that could be due to or from third parties under existing agreements; and our estimates regarding future revenues, research and development expenses, capital requirements and payments to third parties. These statements are based upon our current expectations and speak only as of the date hereof. Our actual results may differ materially and adversely from those expressed in any forward-looking statements as a result of numerous factors and uncertainties, including the safety and efficacy of our product candidates, decisions of regulatory authorities and the timing thereof, the duration and impact of regulatory delays in our clinical programs, our ability to finance our operations, the likelihood and timing of the receipt of future milestone and licensing fees, the future success of our scientific studies, our ability to successfully develop and commercialize drug candidates, the timing for starting and completing clinical trials, rapid technological change in our markets, the enforcement of our intellectual property rights, and the other risks and uncertainties described in our most recent Annual Report on Form 10-K, subsequent Quarterly Reports on Form 10-Q and other documents filed with the Securities and Exchange Commission from time to time. We assume no obligation to update or revise forward-looking statements to reflect new events or circumstances.

Source: Arrowhead Pharmaceuticals, Inc.

More News From Arrowhead Pharmaceuticals, Inc.
2026-06-12 16:36 1mo ago
2026-06-02 08:00 1mo ago
Arrowhead Pharmaceuticals to Participate in Upcoming June 2026 Events
ARWR Arrowhead Pharmaceuticals
FMP Stock News
Original source text
Arrowhead Pharmaceuticals, Inc. (NASDAQ: ARWR) today announced that it is scheduled to participate in the following upcoming events: 2026 Jefferies Global He
2026-06-12 16:36 1mo ago
2026-06-05 14:04 1mo ago
Arrowhead Pharmaceuticals Lines Up SHASTA Readout as REDEMPLO Launch Gains Traction
ARWR Arrowhead Pharmaceuticals
FMP Stock News
Original source text
Want Diversified Upside in Biotechnology? Check out LABUArrowhead Pharmaceuticals NASDAQ: ARWR executives outlined upcoming clinical catalysts, early commercial trends and pipeline priorities during a Jefferies fireside chat, with Chief Medical Officer James Hamilton emphasizing that the company remains focused exclusively on siRNA therapeutics through its TRiM, or Targeted RNAi Molecule, platform.

Hamilton said Arrowhead has advanced 20 clinical candidates into various stages of development. Partnered programs include olpasiran with Amgen, fazirsiran with Takeda, hepatitis B and MASH programs with GSK, a broad discovery collaboration with Sarepta and a recently announced discovery collaboration with Novartis. On the wholly owned side, Hamilton highlighted REDEMPLO, which was recently approved for familial chylomicronemia syndrome, as well as plozasiran in severe hypertriglyceridemia, zodasiran in homozygous familial hypercholesterolemia, obesity candidates ARO-ALK7 and ARO-INHBE, and ARO-MAPT for tau-related neurological diseases.

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SHASTA Data Remain on Track for Third Quarter Hamilton said the company remains on schedule to report topline data in the third quarter from SHASTA-3 and SHASTA-4, pivotal studies of plozasiran in severe hypertriglyceridemia. He said the final patients are expected to complete visits “over the next month or so,” but Arrowhead is not narrowing its guidance to a specific month because late acute pancreatitis events or serious adverse events could still require adjudication.

On the acute pancreatitis endpoint, Hamilton said Arrowhead remains “cautiously optimistic” while blinded to the data. He said the company has previously indicated that roughly nine or more acute pancreatitis events, with event rates similar to those seen in CORE and CORE2 studies, would provide around 80% power. He added that events have not appeared “wildly out of our range of expectations,” but said the outcome will not be known until the third-quarter readout.

Hamilton said Arrowhead does not plan changes to its statistical analysis plan and has long planned to pool acute pancreatitis data from SHASTA-3 and SHASTA-4. He also said baseline triglyceride values across the combined studies are about 860, compared with about 600 in the SHASTA-2 study, where the company saw approximately a 70% triglyceride reduction. He said a 10% decline in the placebo group “wouldn’t surprise” him, reflecting diet adherence and potential reversion to the mean.

Safety, Liver Fat and Competitive Context Asked about Ionis’ olezarsen, Hamilton said he expects approval and said acute pancreatitis may be included in the label, though he said it is unclear where such information would appear. He described the CORE and CORE2 data as “really good and really convincing,” particularly on acute pancreatitis.

Hamilton also discussed safety differences between Arrowhead’s siRNA approach and antisense oligonucleotide, or ASO, therapies. He said Arrowhead is not seeing hypersensitivity reactions or thrombocytopenia, which he characterized as more consistent with ASO class effects. On liver fat, Hamilton said Arrowhead did not observe an increase at the 25-milligram dose in SHASTA-2, which he described as the go-to-market dose, though a 2% absolute increase from baseline was seen at a 50-milligram dose the company is no longer using. He said Arrowhead should provide an update on liver fat when it reports severe hypertriglyceridemia data.

REDEMPLO Launch and Pricing Daniel Apel, Arrowhead’s chief financial officer, said the REDEMPLO launch in familial chylomicronemia syndrome is trending better than Ionis’ launch at a similar time point when normalized for price and viewed on a unit basis, though he cautioned against overemphasizing early numbers in an ultra-rare indication. He said there was some pent-up demand from expanded access program switches and some patients switching from TRYNGOLZA, but most demand has been new to class.

Apel said Arrowhead expects continued largely linear growth, primarily from patients naive to the APOC3 class, with some contribution from switchers. He cited REDEMPLO’s three-month dosing schedule, potency and lack of warnings, precautions or contraindications as factors the company believes will support physician choice.

On pricing, Apel said payer feedback has been positive after Arrowhead reduced REDEMPLO’s wholesale acquisition cost to $45,000 from $60,000. He said the move maintained a premium position while keeping the therapy within a range that payers view as cost comparable, and said payer discussions are proceeding well and aligned with the approved label.

Obesity, MASH and CNS Programs Hamilton said recent EASL data for ARO-INHBE showed about a 40% reduction in liver fat from baseline in patients with hepatic steatosis, supporting a potential monotherapy pathway in MASH. He said Arrowhead is also evaluating ARO-INHBE with GLP-1 therapy, especially in diabetics, where it has seen additional weight loss versus GLP-1 alone.

Hamilton said ARO-ALK7 and ARO-INHBE studies are fully enrolled with about 240 total patients across monotherapy and tirzepatide combination cohorts. Additional ARO-INHBE cohorts include higher-dose monotherapy in Type 2 diabetics and combinations with 5 mg and 15 mg tirzepatide. He said Arrowhead plans more ARO-ALK7 data in the second half, focusing on body composition, weight loss, visceral fat and lean mass.

For ARO-MAPT, Hamilton said later-year data will focus on safety and tau knockdown in healthy volunteers, with patient data likely next year. He said Arrowhead would like to see total tau knockdown in cerebrospinal fluid comparable to the 50% to 60% reported by Ionis in Alzheimer’s patients, and said successful subcutaneous CNS knockdown would be important for the broader platform.

Additional Catalysts Hamilton said Arrowhead plans to report third-quarter data from its APOC3-PCSK9 dimer program in patients with mixed hyperlipidemia. He said initial success would include total ApoB reductions of about 40% or better, with the company ultimately aiming to move toward outcomes testing after establishing long-term safety and dose.

Apel said Arrowhead is not planning to out-license additional programs or disclose new business development activity. He listed upcoming catalysts including SHASTA-3 and SHASTA-4 data, dimer data, ARO-MAPT cerebrospinal fluid data, additional obesity data and potential full enrollment of the zodasiran program later this year. No specific cash runway update was provided in the discussion.

About Arrowhead Pharmaceuticals NASDAQ: ARWRArrowhead Pharmaceuticals, Inc is a clinical-stage biopharmaceutical company focused on the discovery, development and commercialization of RNA interference (RNAi) therapeutics. Since its founding in 2008, Arrowhead has leveraged its proprietary delivery platform—known internally as the Advanced RNAi Compound (ARC) technology—to silence disease-causing genes in patients suffering from genetically defined diseases. The company's approach aims to offer durable, targeted treatments across a range of therapeutic areas.

The company's pipeline includes multiple candidates in various stages of development.

This instant news alert was generated by narrative science technology and financial data from MarketBeat in order to provide readers with the fastest reporting and unbiased coverage. Please send any questions or comments about this story to [email protected].

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2026-06-12 16:36 1mo ago
2026-06-10 15:02 1mo ago
Arrowhead Pharmaceuticals, Inc. (ARWR) Presents at Goldman Sachs 47th Annual Global Healthcare Conference 2026 Prepared Remarks Transcript
ARWR Arrowhead Pharmaceuticals
FMP Stock News
Original source text
Arrowhead Pharmaceuticals, Inc. (ARWR) Presents at Goldman Sachs 47th Annual Global Healthcare Conference 2026 Prepared Remarks Transcript
2026-06-12 16:36 1mo ago
2026-03-14 04:37 4mo ago
Innospec: Oilfield Services Bound For A Recovery
IOSP Innospec
FMP Stock News
Original source text
Innospec is positioned as a likely beneficiary of energy shortages and rising oil prices, supplying vital chemicals for oil extraction and refining. IOSP trades at a 50% discount to sector P/E and EV/EBITDA multiples, despite a debt-free balance sheet and strong free cash flow generation. Operational catalysts include potential recovery in oilfield services, resolution of the Mexico crisis, and increased demand from geopolitical disruptions.
2026-06-12 16:36 1mo ago
2026-03-19 12:31 4mo ago
Innospec (IOSP) Down 21.8% Since Last Earnings Report: Can It Rebound?
IOSP Innospec
FMP Stock News
Original source text
It has been about a month since the last earnings report for Innospec (IOSP - Free Report) . Shares have lost about 21.8% in that time frame, underperforming the S&P 500.

But investors have to be wondering, will the recent negative trend continue leading up to its next earnings release, or is Innospec due for a breakout? Well, first let's take a quick look at its latest earnings report in order to get a better handle on the recent drivers for Innospec Inc. before we dive into how investors and analysts have reacted as of late.

Key HighlightsEarnings per share (as reported) for the fourth quarter of 2025 improved to $1.91 from a loss of $2.80 a year ago, which was impacted by a UK pension scheme buyout.

Adjusted earnings per share rose 6% to $1.50 from $1.41 a year ago, beating the consensus mark of $1.26.

Revenues for the fourth quarter declined 2% year over year to $455.6 million, missing the Zacks Consensus Estimate of $477 million.

Adjusted EBITDA declined 2% year over year to $55.7 million. Operating income increased 14% to $46.8 million.

Segment PerformanceFuel Specialties revenues rose 1% year over year to $194.1 million, driven by volume growth of 8% offset by an adverse price/mix of 10% and a positive currency impact of 3%. Gross margin expanded 0.3 percentage points to 34.7% and operating income increased 7% to $37.2 million.

Performance Chemicals revenues were flat at $168.4 million as volume declines of 7% were offset by positive price/mix of 3% and currency of 4%. Gross margin compressed 4.6 percentage points to 18.1%, and operating income fell 14% to $17.7 million.

Oilfield Services revenues declined 12% to $93.1 million, reflecting lower U.S. completions and reduced Middle East activity. Gross margin improved 1.8 percentage points to 31.9% on richer sales mix and lower overheads and operating income increased 9% to $8.2 million.

Financials and OutlookOperating cash flow reached $61.4 million with free cash flow of $40.9 million versus $5.1 million in the year-ago quarter. The company ended 2025 with net cash of $292.5 million and no debt.

In the fourth quarter, the adjusted effective tax rate was 24.1%. The company expects a 2026 effective tax rate of roughly 26% and corporate costs of around $20 million per quarter.

Performance Chemicals’ growth is expected to be roughly flat for 2026, with margin improvement building into the second half through pricing mechanisms, manufacturing efficiencies and higher-margin new products.

For Oilfield Services, the company targets 2026 operating income growth with roughly 5-7% full-year revenue growth, led by Middle East activity and the DRA ramp. Fuel Specialties is expected to remain a stable contributor with long-term growth of 2-3%. A historic late-January 2026 winter storm is expected to impact near-term results, with Performance Chemicals' first-quarter operating income around $10-$11 million and Oilfield Services' operating income of around $5-$6 million.

How Have Estimates Been Moving Since Then?In the past month, investors have witnessed a downward trend in estimates revision.

The consensus estimate has shifted -23.33% due to these changes.

VGM ScoresAt this time, Innospec has a subpar Growth Score of D, however its Momentum Score is doing a bit better with a C. Charting a somewhat similar path, the stock was allocated a score of B on the value side, putting it in the second quintile for this investment strategy.

Overall, the stock has an aggregate VGM Score of C. If you aren't focused on one strategy, this score is the one you should be interested in.

OutlookEstimates have been broadly trending downward for the stock, and the magnitude of this revision indicates a downward shift. It's no surprise Innospec has a Zacks Rank #4 (Sell). We expect a below average return from the stock in the next few months.
2026-06-12 16:36 1mo ago
2026-03-31 03:21 3mo ago
Allspring Global Investments Holdings LLC Sells 35,246 Shares of Innospec Inc. $IOSP
IOSP Innospec
FMP Stock News
Original source text
Posted by Defense World Staff on Mar 31st, 2026

Allspring Global Investments Holdings LLC decreased its stake in shares of Innospec Inc. (NASDAQ:IOSP – Free Report) by 1.5% in the 4th quarter, according to the company in its most recent filing with the Securities & Exchange Commission. The firm owned 2,356,503 shares of the specialty chemicals company’s stock after selling 35,246 shares during the quarter. Allspring Global Investments Holdings LLC owned about 9.51% of Innospec worth $179,754,000 as of its most recent filing with the Securities & Exchange Commission.

Other hedge funds also recently modified their holdings of the company. Wedge Capital Management L L P NC lifted its position in shares of Innospec by 20.5% during the 4th quarter. Wedge Capital Management L L P NC now owns 19,699 shares of the specialty chemicals company’s stock valued at $1,508,000 after acquiring an additional 3,354 shares during the period. SG Americas Securities LLC increased its stake in Innospec by 291.0% in the fourth quarter. SG Americas Securities LLC now owns 75,814 shares of the specialty chemicals company’s stock valued at $5,803,000 after purchasing an additional 56,425 shares in the last quarter. Assenagon Asset Management S.A. raised its holdings in shares of Innospec by 37.7% during the fourth quarter. Assenagon Asset Management S.A. now owns 178,204 shares of the specialty chemicals company’s stock valued at $13,640,000 after purchasing an additional 48,807 shares during the period. Wealth Enhancement Advisory Services LLC raised its holdings in shares of Innospec by 25.8% during the fourth quarter. Wealth Enhancement Advisory Services LLC now owns 9,223 shares of the specialty chemicals company’s stock valued at $725,000 after purchasing an additional 1,892 shares during the period. Finally, Allworth Financial LP boosted its position in shares of Innospec by 31.0% during the 3rd quarter. Allworth Financial LP now owns 588 shares of the specialty chemicals company’s stock worth $45,000 after purchasing an additional 139 shares in the last quarter. Institutional investors own 96.64% of the company’s stock.

Insiders Place Their Bets In other Innospec news, Director Larry Padfield sold 594 shares of the business’s stock in a transaction on Friday, February 27th. The stock was sold at an average price of $76.56, for a total value of $45,476.64. Following the transaction, the director owned 9,453 shares of the company’s stock, valued at approximately $723,721.68. The trade was a 5.91% decrease in their ownership of the stock. The transaction was disclosed in a document filed with the Securities & Exchange Commission, which is accessible through this link. Also, SVP David B. Jones sold 1,028 shares of the company’s stock in a transaction on Tuesday, March 3rd. The shares were sold at an average price of $75.64, for a total value of $77,757.92. Following the completion of the transaction, the senior vice president owned 14,693 shares of the company’s stock, valued at $1,111,378.52. This trade represents a 6.54% decrease in their position. The SEC filing for this sale provides additional information. Over the last three months, insiders have sold 4,989 shares of company stock valued at $391,889. 1.31% of the stock is owned by insiders.

Innospec Stock Performance Shares of IOSP stock opened at $73.19 on Tuesday. The company has a market capitalization of $1.82 billion, a price-to-earnings ratio of 15.64, a PEG ratio of 1.90 and a beta of 0.90. Innospec Inc. has a 52-week low of $65.51 and a 52-week high of $96.38. The company has a 50-day simple moving average of $77.77 and a two-hundred day simple moving average of $77.03.

Innospec (NASDAQ:IOSP – Get Free Report) last announced its earnings results on Tuesday, February 17th. The specialty chemicals company reported $1.50 earnings per share for the quarter, topping analysts’ consensus estimates of $1.26 by $0.24. The firm had revenue of $455.60 million for the quarter, compared to the consensus estimate of $460.87 million. Innospec had a return on equity of 10.18% and a net margin of 6.56%.The company’s revenue was down 2.4% compared to the same quarter last year. During the same quarter in the previous year, the business earned $1.41 EPS. On average, sell-side analysts forecast that Innospec Inc. will post 6.18 EPS for the current fiscal year.

Analysts Set New Price Targets Several analysts have recently commented on the company. Zacks Research downgraded Innospec from a “hold” rating to a “strong sell” rating in a research note on Thursday, February 19th. Wall Street Zen upgraded Innospec from a “hold” rating to a “buy” rating in a report on Saturday, December 13th. Finally, Weiss Ratings raised Innospec from a “sell (d+)” rating to a “hold (c-)” rating in a research note on Thursday, February 19th. One research analyst has rated the stock with a Hold rating and one has issued a Sell rating to the company. Based on data from MarketBeat.com, the stock has a consensus rating of “Reduce”.

View Our Latest Stock Report on Innospec

About Innospec (Free Report)

Innospec Incorporated (NASDAQ: IOSP) is a global specialty chemicals company headquartered in Cleveland, Ohio. The company operates through three principal business segments: Fuel Specialties, Oilfield Services, and Performance Chemicals. In the Fuel Specialties segment, Innospec develops and supplies additives designed to enhance octane levels, improve combustion efficiency, reduce emissions and prevent deposit formation in gasoline and diesel engines. Its Oilfield Services division provides chemical technologies—such as surfactants, corrosion inhibitors and demulsifiers—to support exploration, drilling, production optimization and enhanced oil recovery operations.

See Also Five stocks we like better than Innospec Want to see what other hedge funds are holding IOSP? Visit HoldingsChannel.com to get the latest 13F filings and insider trades for Innospec Inc. (NASDAQ:IOSP – Free Report).

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2026-06-12 16:36 1mo ago
2026-04-27 13:11 3mo ago
Will Innospec (IOSP) Beat Estimates Again in Its Next Earnings Report?
IOSP Innospec
FMP Stock News
Original source text
Looking for a stock that has been consistently beating earnings estimates and might be well positioned to keep the streak alive in its next quarterly report? Innospec (IOSP - Free Report) , which belongs to the Zacks Chemical - Diversified industry, could be a great candidate to consider.

When looking at the last two reports, this specialty chemicals company has recorded a strong streak of surpassing earnings estimates. The company has topped estimates by 13.89%, on average, in the last two quarters.

For the last reported quarter, Innospec came out with earnings of $1.5 per share versus the Zacks Consensus Estimate of $1.26 per share, representing a surprise of 19.05%. For the previous quarter, the company was expected to post earnings of $1.03 per share and it actually produced earnings of $1.12 per share, delivering a surprise of 8.74%.

Price and EPS Surprise

For Innospec, estimates have been trending higher, thanks in part to this earnings surprise history. And when you look at the stock's positive Zacks Earnings ESP (Expected Surprise Prediction), it's a great indicator of a future earnings beat, especially when combined with its solid Zacks Rank.

Our research shows that stocks with the combination of a positive Earnings ESP and a Zacks Rank #3 (Hold) or better produce a positive surprise nearly 70% of the time. In other words, if you have 10 stocks with this combination, the number of stocks that beat the consensus estimate could be as high as seven.

The Zacks Earnings ESP compares the Most Accurate Estimate to the Zacks Consensus Estimate for the quarter; the Most Accurate Estimate is a version of the Zacks Consensus whose definition is related to change. The idea here is that analysts revising their estimates right before an earnings release have the latest information, which could potentially be more accurate than what they and others contributing to the consensus had predicted earlier.

Innospec currently has an Earnings ESP of +2.46%, which suggests that analysts have recently become bullish on the company's earnings prospects. This positive Earnings ESP when combined with the stock's Zacks Rank #3 (Hold) indicates that another beat is possibly around the corner. We expect the company's next earnings report to be released on May 7, 2026.

Investors should note, however, that a negative Earnings ESP reading is not indicative of an earnings miss, but a negative value does reduce the predictive power of this metric.

Many companies end up beating the consensus EPS estimate, but that may not be the sole basis for their stocks moving higher. On the other hand, some stocks may hold their ground even if they end up missing the consensus estimate.

Because of this, it's really important to check a company's Earnings ESP ahead of its quarterly release to increase the odds of success. Make sure to utilize our Earnings ESP Filter to uncover the best stocks to buy or sell before they've reported.
2026-06-12 16:36 1mo ago
2026-04-30 10:06 2mo ago
Is the Options Market Predicting a Spike in Innospec Stock?
IOSP Innospec
FMP Stock News
Original source text
Image: Bigstock

Read MoreHide Full Article

Investors in Innospec Inc. (IOSP - Free Report) need to pay close attention to the stock based on moves in the options market lately. That is because the Jun 18, 2026 $80 Call had some of the highest implied volatility of all equity options today.

What is Implied Volatility?Implied volatility shows how much movement the market is expecting in the future. Options with high levels of implied volatility suggest that investors in the underlying stocks are expecting a big move in one direction or the other. It could also mean there is an event coming up soon that may cause a big rally or a huge sell-off. However, implied volatility is only one piece of the puzzle when putting together an options trading strategy.

What do the Analysts Think?Clearly, options traders are pricing in a big move for Innospec shares, but what is the fundamental picture for the company? Currently, Innospec is a Zacks Rank #4 (Sell) in the Chemical - Diversified industry that ranks in the Bottom 34% of our Zacks Industry Rank. Over the last 30 days, no analysts have increased their earnings estimates for the current quarter, while one analyst has revised the estimate downward. The net effect has taken our Zacks Consensus Estimate for the current quarter from $1.04 per share to $1.02 in that period.

Given the way analysts feel about Innospec right now, this huge implied volatility could mean there’s a trade developing. Oftentimes, options traders look for options with high levels of implied volatility to sell premium. This is a strategy many seasoned traders use because it captures decay. At expiration, the hope for these traders is that the underlying stock does not move as much as originally expected.

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Published in basic-materials
2026-06-12 16:36 1mo ago
2026-04-30 11:01 2mo ago
Analysts Estimate Innospec (IOSP) to Report a Decline in Earnings: What to Look Out for
IOSP Innospec
FMP Stock News
Original source text
The market expects Innospec (IOSP - Free Report) to deliver a year-over-year decline in earnings on lower revenues when it reports results for the quarter ended March 2026. This widely-known consensus outlook is important in assessing the company's earnings picture, but a powerful factor that might influence its near-term stock price is how the actual results compare to these estimates.

The stock might move higher if these key numbers top expectations in the upcoming earnings report, which is expected to be released on May 7. On the other hand, if they miss, the stock may move lower.

While management's discussion of business conditions on the earnings call will mostly determine the sustainability of the immediate price change and future earnings expectations, it's worth having a handicapping insight into the odds of a positive EPS surprise.

Zacks Consensus EstimateThis specialty chemicals company is expected to post quarterly earnings of $1.02 per share in its upcoming report, which represents a year-over-year change of -28.2%.

Revenues are expected to be $432.15 million, down 2% from the year-ago quarter.

Estimate Revisions TrendThe consensus EPS estimate for the quarter has been revised 6.01% lower over the last 30 days to the current level. This is essentially a reflection of how the covering analysts have collectively reassessed their initial estimates over this period.

Investors should keep in mind that an aggregate change may not always reflect the direction of estimate revisions by each of the covering analysts.

Price, Consensus and EPS Surprise

Earnings WhisperEstimate revisions ahead of a company's earnings release offer clues to the business conditions for the period whose results are coming out. Our proprietary surprise prediction model -- the Zacks Earnings ESP (Expected Surprise Prediction) -- has this insight at its core.

The Zacks Earnings ESP compares the Most Accurate Estimate to the Zacks Consensus Estimate for the quarter; the Most Accurate Estimate is a more recent version of the Zacks Consensus EPS estimate. The idea here is that analysts revising their estimates right before an earnings release have the latest information, which could potentially be more accurate than what they and others contributing to the consensus had predicted earlier.

Thus, a positive or negative Earnings ESP reading theoretically indicates the likely deviation of the actual earnings from the consensus estimate. However, the model's predictive power is significant for positive ESP readings only.

A positive Earnings ESP is a strong predictor of an earnings beat, particularly when combined with a Zacks Rank #1 (Strong Buy), 2 (Buy) or 3 (Hold). Our research shows that stocks with this combination produce a positive surprise nearly 70% of the time, and a solid Zacks Rank actually increases the predictive power of Earnings ESP.

Please note that a negative Earnings ESP reading is not indicative of an earnings miss. Our research shows that it is difficult to predict an earnings beat with any degree of confidence for stocks with negative Earnings ESP readings and/or Zacks Rank of 4 (Sell) or 5 (Strong Sell).

How Have the Numbers Shaped Up for Innospec?For Innospec, the Most Accurate Estimate is higher than the Zacks Consensus Estimate, suggesting that analysts have recently become bullish on the company's earnings prospects. This has resulted in an Earnings ESP of +2.46%.

On the other hand, the stock currently carries a Zacks Rank of #4.

So, this combination makes it difficult to conclusively predict that Innospec will beat the consensus EPS estimate.

Does Earnings Surprise History Hold Any Clue?Analysts often consider to what extent a company has been able to match consensus estimates in the past while calculating their estimates for its future earnings. So, it's worth taking a look at the surprise history for gauging its influence on the upcoming number.

For the last reported quarter, it was expected that Innospec would post earnings of $1.26 per share when it actually produced earnings of $1.50, delivering a surprise of +19.05%.

Over the last four quarters, the company has beaten consensus EPS estimates four times.

Bottom LineAn earnings beat or miss may not be the sole basis for a stock moving higher or lower. Many stocks end up losing ground despite an earnings beat due to other factors that disappoint investors. Similarly, unforeseen catalysts help a number of stocks gain despite an earnings miss.

That said, betting on stocks that are expected to beat earnings expectations does increase the odds of success. This is why it's worth checking a company's Earnings ESP and Zacks Rank ahead of its quarterly release. Make sure to utilize our Earnings ESP Filter to uncover the best stocks to buy or sell before they've reported.

Innospec doesn't appear a compelling earnings-beat candidate. However, investors should pay attention to other factors too for betting on this stock or staying away from it ahead of its earnings release.

An Industry Player's Expected ResultsAmong the stocks in the Zacks Chemical - Diversified industry, Albemarle (ALB - Free Report) , is soon expected to post earnings of $1.24 per share for the quarter ended March 2026. This estimate indicates a year-over-year change of +788.9%. This quarter's revenue is expected to be $1.33 billion, up 23.1% from the year-ago quarter.

Over the last 30 days, the consensus EPS estimate for Albemarle has been revised 18.4% up to the current level. Nevertheless, the company now has an Earnings ESP of +20.12%, reflecting a higher Most Accurate Estimate.

This Earnings ESP, combined with its Zacks Rank #3 (Hold), suggests that Albemarle will most likely beat the consensus EPS estimate. Over the last four quarters, the company surpassed consensus EPS estimates three times.

Stay on top of upcoming earnings announcements with the Zacks Earnings Calendar.
2026-06-12 16:36 1mo ago
2026-05-07 16:45 2mo ago
Innospec Reports First Quarter 2026 Financial Results
IOSP Innospec
FMP Stock News
Original source text
Continued strength in Fuel Specialties offset negative US winter storm impacts in other businesses

Increasing confidence for sequential operating income and margin growth in Performance Chemicals and Oilfield Services

Dividend increased by 10 percent; $6.2 million in share repurchases made in the quarter

New $75 million buyback authorization

GAAP EPS of $1.22 and adjusted non-GAAP EPS of $1.05

ENGLEWOOD, Colo., May 07, 2026 (GLOBE NEWSWIRE) -- Innospec Inc. (NASDAQ: IOSP) today announced its financial results for the first quarter ended March 31, 2026.   The Company declared its semi-annual dividend of 92 cents per common share for the first half of this year, representing an increase of 10 percent. This dividend will be paid on May 29, 2026 to shareholders of record on May 19, 2026.

Total revenues for the first quarter were $453.2 million, an increase of 3 percent from $440.8 million in the corresponding period last year. Net income attributable to Innospec for the quarter was $30.4 million or $1.22 per diluted share compared to $32.8 million or $1.31 per diluted share recorded in the corresponding period last year. Adjusted EBITDA for the quarter was $43.7 million compared to $54.0 million reported in the same period a year ago.

Results for this quarter include some special items, which are summarized in the table below. Excluding these items, adjusted non-GAAP EPS in the first quarter was $1.05 per diluted share, compared to $1.42 per diluted share a year ago.

Cash from operating activities was $17.6 million before capital expenditures of $8.6 million. The quarter closed with net cash of $289.1 million.

Adjusted EBITDA and net income attributable to Innospec excluding special items, and related per-share amounts, together with net cash, are non-GAAP financial measures that are defined and reconciled with GAAP results herein and in the schedules below.

  Quarter ended March 31, 2026Quarter ended March 31, 2025          (in millions, except share and per share data) Net income attributable to Innospec Diluted EPS Net income attributable to Innospec Diluted EPS           Reported GAAP amounts$30.4$1.22$32.8$1.31           Adjustment to fair value of contingent consideration (4.7) (0.19) 0.7 0.03 Foreign currency exchange gains (1.9) (0.08) (0.3) (0.01) Legacy costs of closed operations 1.7 0.07 0.6 0.02 Amortization of acquired intangible assets 0.8 0.03 1.7 0.07   (4.1) (0.17) 2.7 0.11           Adjusted non-GAAP amounts$26.3$1.05$35.5$1.42            Commenting on the first quarter results, Patrick S. Williams, President and Chief Executive Officer, said,

“This was a mixed quarter for Innospec with continued strong results in Fuel Specialties partially offsetting the negative impacts of the January 2026 US winter storm on Performance Chemicals and Oilfield Services.

Performance Chemicals sales were broadly flat with last year, but margins and operating income were significantly impacted by a shutdown of the North Carolina plants due to the US winter storm. We are prioritizing plant repairs in order to meet customer requirements. In parallel, we continue to execute on a range of other topline and margin opportunities identified in the business. We expect these combined efforts to drive sequential growth in the second quarter.

Fuel Specialties had another strong quarter with sales growth and margins that remained at the upper end of our target range. As expected, the business has continued to deliver consistently strong results as our team advances on a broad set of regional and end-market opportunities in traditional fuel, renewable fuel and non-fuel applications.

Oilfield Services operating income and margins improved on the prior year, but overall performance was negatively impacted by the US winter storm. While the Middle East conflict may delay the planned expansion in the region, we remain focused on driving incremental growth from our recent DRA expansion and other opportunities in our completions and production segments. We are cautiously optimistic that these efforts will drive sequential improvement in the second quarter and leave us well positioned for further improvement in the second half of 2026.”

Revenues in Performance Chemicals of $169.4 million were up 1 percent over the first quarter of last year as volume reductions of 9 percent were offset by a positive price/mix of 1 percent and favorable currency impact of 9 percent.   Gross margins of 16.8 percent decreased by 4.2 percentage points from the same quarter last year. Operating income of $10.7 million decreased 46 percent from $19.8 million in the corresponding prior year period.

Revenues in Fuel Specialties of $181.6 million were up 7 percent from $170.3 million in the first quarter of last year with volume growth of 10 percent and a positive currency impact of 6 percent offsetting a negative price/mix of 9 percent. Gross margins of 35.4 percent decreased by 0.3 percentage points over last year. Operating income of $37.8 million was up 2 percent from $36.9 million a year ago.  

Revenues in Oilfield Services of $102.2 million for the quarter were consistent compared with the first quarter of last year. Gross margins of 30.1 percent increased by 1.7 percentage points from the same quarter last year on a richer sales mix.   Operating income of $5.6 million increased 37 percent from $4.1 million in the prior year period.

Corporate costs for the quarter were $22.3 million, compared with $17.7 million a year ago. The effective tax rate for the quarter was 22.8 percent compared to 25.7 percent in the same period last year.

For the quarter, net cash provided by operating activities was $17.6 million compared to $28.3 million a year ago. As of March 31, 2026, Innospec had $289.1 million in cash and cash equivalents and no debt.

Mr. Williams concluded,

“While the Middle East conflict is creating significant market uncertainty, we are seeing increased opportunities to deliver stand-out service and security of supply for all our customers. Our teams remain focused on elements within our control as we have in prior similar cycles. In parallel, margin enhancement, new technology commercialization and other opportunities remain the priority across our businesses, and we are optimistic about the impact that these actions will have on future results.

Operating cash generation was again positive in the quarter, and our net cash position closed at over $289 million. We have significant balance sheet flexibility for dividend growth, buybacks, organic investment and M&A. This quarter our Board approved a further 10 percent increase in our semi-annual dividend to 92 cents per share, and we completed $6.2 million in share repurchases. Additionally, the Board approved a new $75 million buyback authorization to further enhance shareholder return flexibility.”  

Use of Non-GAAP Financial Measures

The information presented in this press release includes financial measures that are not calculated or presented in accordance with Generally Accepted Accounting Principles in the United States (GAAP). These non-GAAP financial measures comprise adjusted EBITDA, net income attributable to Innospec excluding special items and related per share amounts together with net cash. Adjusted EBITDA is net income attributable to Innospec per our consolidated financial statements adjusted for the exclusion of interest income, net, income taxes, depreciation and amortization, foreign currency exchange gains, legacy costs of closed operations and adjustment to fair value of contingent consideration. Net income attributable to Innospec and diluted EPS, excluding special items, per our consolidated financial statements are adjusted for the exclusion of adjustment to fair value of contingent consideration, foreign currency exchange gains, legacy costs of closed operations and amortization of acquired intangible assets. Net cash is cash and cash equivalents less total debt. Reconciliations of these non-GAAP financial measures to their most directly comparable GAAP financial measures are provided herein and in the schedules below.

The Company believes that such non-GAAP financial measures provide useful information to investors and may assist them in evaluating the Company’s underlying performance and identifying operating trends. In addition, these non-GAAP measures address questions the Company routinely receives from analysts and investors and the Company has determined that it is appropriate to make this data available to all investors. While the Company believes that such measures are useful in evaluating the Company’s performance, investors should not consider them to be a substitute for financial measures prepared in accordance with GAAP. In addition, these non-GAAP financial measures may differ from similarly titled non-GAAP financial measures used by other companies and do not provide a comparable view of the Company’s performance relative to other companies in similar industries. Management uses adjusted EPS (the most directly comparable GAAP financial measure for which is GAAP EPS) and net income attributable to Innospec excluding special items and adjusted EBITDA (the most directly comparable GAAP financial measure for which is GAAP net income attributable to Innospec) to allocate resources and evaluate the performance of the Company’s operations and has provided a reconciliation of adjusted EBITDA and net income attributable to Innospec excluding special items, and related per share amounts, to GAAP net income attributable to Innospec herein and in the schedules below.

About Innospec Inc.

Innospec Inc. is an international specialty chemicals company with approximately 2,450 employees in 22 countries. Innospec manufactures and supplies a wide range of specialty chemicals to markets in the Americas, Europe, the Middle East, Africa and Asia-Pacific.  The Performance Chemicals business creates innovative technology-based solutions for our customers in the Personal Care, Home Care, Agrochemical, Mining and Industrial markets. The Fuel Specialties business specializes in manufacturing and supplying fuel additives that improve fuel efficiency, boost engine performance and reduce harmful emissions. Oilfield Services provides specialty chemicals to all elements of the oil and gas exploration and production industry. 

Forward-Looking Statements

This press release contains certain "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995.  All statements other than statements of historical facts included or incorporated herein may constitute forward-looking statements.  Such forward-looking statements include statements (covered by words like “expects,” “estimates,” “anticipates,” “may,” “could,” “believes,” “feels,” “plans,” “intends,” “outlook” or similar words or expressions, for example) which relate to earnings, growth potential, operating performance, events or developments that we expect or anticipate will or may occur in the future.  Although forward-looking statements are believed by management to be reasonable when made, they are subject to certain risks, uncertainties and assumptions, and our actual performance or results may differ materially from these forward-looking statements.  Additional information regarding risks, uncertainties and assumptions relating to Innospec and affecting our business operations and prospects are described in Innospec’s Annual Report on Form 10-K for the year ended December 31, 2025 and other reports filed with the U.S. Securities and Exchange Commission.  You are urged to review our discussion of risks and uncertainties that could cause actual results to differ from forward-looking statements under the heading "Risk Factors” in such reports. Innospec undertakes no obligation to publicly update or revise any forward-looking statements, whether as a result of new information, future events or otherwise.

Contacts:

Corbin Barnes
Innospec Inc.
+1-303-792-5554
[email protected]

INNOSPEC INC. AND SUBSIDIARIES
CONDENSED CONSOLIDATED STATEMENTS OF INCOME
 Schedule 1    Three Months Ended   March 31(in millions, except share and per share data)  2026 2025      Net sales $453.2$440.8Cost of goods sold  (329.7) (315.7)Gross profit  123.5 125.1      Operating expenses:     Selling, general and administrative  (78.5) (69.3)Research and development  (13.2) (12.7)Adjustment to fair value of contingent consideration  4.7 (0.7)Profit on disposal of property, plant and equipment  - 0.1Total operating expenses  (87.0) (82.6)Operating income  36.5 42.5Other income, net  2.6 0.3Interest income, net  0.8 2.4Income before income taxes  39.9 45.2Income taxes  (9.1) (11.6)Net income  30.8 33.6Net income attributable to non-controlling interests  (0.4) (0.8)Net income attributable to Innospec $30.4$32.8      Earnings per share:     Basic $1.23$1.31Diluted $1.22$1.31      Weighted average shares outstanding (in thousands):     Basic  24,776 24,970Diluted  24,844 25,102       INNOSPEC INC. AND SUBSIDIARIES
Schedule 2A
 SEGMENTAL ANALYSIS OF RESULTS  Three Months Ended   March 31(in millions)  2026 2025      Net sales:     Performance Chemicals $169.4$168.4Fuel Specialties  181.6 170.3Oilfield Services  102.2 102.1   453.2 440.8      Gross profit:     Performance Chemicals  28.4 35.3Fuel Specialties  64.3 60.8Oilfield Services  30.8 29.0   123.5 125.1      Operating income:     Performance Chemicals  10.7 19.8Fuel Specialties  37.8 36.9Oilfield Services  5.6 4.1Corporate costs  (22.3) (17.7)   31.8 43.1Adjustment to fair value of contingent consideration  4.7 (0.7)Profit on disposal of property, plant and equipment  - 0.1Total operating income $36.5$42.5       Schedule 2B NON-GAAP MEASURES  Three Months Ended March 31(in millions)  2026 2025      Net income attributable to Innospec $30.4$32.8Interest income, net  (0.8) (2.4)Income taxes  9.1 11.6Depreciation and amortization  9.9 10.9Foreign currency exchange gains  (2.5) (0.4)Legacy costs of closed operations  2.3 0.8Adjustment to fair value of contingent consideration  (4.7) 0.7Adjusted EBITDA $43.7$54.0       Schedule 3INNOSPEC INC. AND SUBSIDIARIES
CONDENSED CONSOLIDATED BALANCE SHEETS
 (in millions)

  March 31,
2026 December 31,
2025Assets         Current assets:     Cash and cash equivalents $289.1$292.5Trade and other accounts receivable  354.2 342.3Inventories  321.5 329.3Prepaid expenses  16.9 20.1Prepaid income taxes  10.6 13.1Other current assets  6.8 7.3Total current assets  999.1 1,004.6      Net property, plant and equipment  285.7 286.1Operating lease right-of-use assets  50.6 52.7Goodwill  399.1 399.0Other intangible assets  68.9 67.7Deferred tax assets  13.0 13.6Other non-current assets  3.4 8.7Total assets $1,819.8$1,832.4Liabilities and Stockholders’ Equity           Current liabilities:     Accounts payable $138.5$174.7Accrued liabilities  169.3 152.3Current portion of operating lease liabilities  15.1 15.9Current portion of plant closure provisions  4.9 4.9Current portion of acquisition-related contingent consideration  2.7 7.0Accrued income taxes  4.3 5.3Total current liabilities  334.8 360.1      Operating lease liabilities, net of current portion  35.5 36.8Plant closure provisions, net of current portion  60.8 60.2Deferred tax liabilities  17.9 19.1Pension liabilities and post-employment benefits  12.8 13.2Acquisition-related contingent consideration, net of current portion  1.3 1.3Other non-current liabilities  4.5 8.8Equity  1,352.2 1,332.9Total liabilities and equity $1,819.8$1,832.4       Schedule 4
INNOSPEC INC. AND SUBSIDIARIES
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS
    Three Months Ended
March 31(in millions)  2026 2025Cash Flows from Operating Activities           Net income attributable to Innospec $30.4$32.8Adjustments to reconcile net income to cash provided by operating activities:     Depreciation and amortization  9.9 10.9Adjustment to fair value of contingent consideration  (4.7) 0.7Deferred taxes  (0.7) (0.3)Profit on disposal of property, plant and equipment  - (0.1)Movements on defined benefit pension plans  (0.2) 1.3Stock option compensation  1.6 1.9Changes in working capital  (22.3) (21.6)Movements in plant closure provisions  1.5 (0.4)Movements in income taxes  0.4 4.3Movements in other assets and liabilities  1.7 (1.2)Net cash provided by operating activities  17.6 28.3Cash Flows from Investing Activities           Capital expenditures  (8.9) (8.4)Proceeds on disposal of property, plant and equipment  0.3 0.1Internally developed software  (5.1) (7.2)Net cash used in investing activities  (13.7) (15.5)Cash Flows from Financing Activities           Non-controlling interest  0.4 0.8Issue of treasury stock  0.1 0.2Repurchase of common stock  (7.1) (4.8)Net cash used in financing activities  (6.6) (3.8)      Effect of foreign currency exchange rate changes on cash  (0.7) 1.6Net change in cash and cash equivalents  (3.4) 10.6Cash and cash equivalents at beginning of period  292.5 289.2Cash and cash equivalents at end of period $289.1$299.8      
2026-06-12 16:36 1mo ago
2026-05-07 20:05 2mo ago
Innospec (IOSP) Surpasses Q1 Earnings and Revenue Estimates
IOSP Innospec
FMP Stock News
Original source text
Innospec (IOSP - Free Report) came out with quarterly earnings of $1.05 per share, beating the Zacks Consensus Estimate of $1.02 per share. This compares to earnings of $1.42 per share a year ago. These figures are adjusted for non-recurring items.

This quarterly report represents an earnings surprise of +3.45%. A quarter ago, it was expected that this specialty chemicals company would post earnings of $1.26 per share when it actually produced earnings of $1.5, delivering a surprise of +19.05%.

Over the last four quarters, the company has surpassed consensus EPS estimates four times.

Innospec, which belongs to the Zacks Chemical - Diversified industry, posted revenues of $453.2 million for the quarter ended March 2026, surpassing the Zacks Consensus Estimate by 4.87%. This compares to year-ago revenues of $440.8 million. The company has topped consensus revenue estimates three times over the last four quarters.

The sustainability of the stock's immediate price movement based on the recently-released numbers and future earnings expectations will mostly depend on management's commentary on the earnings call.

Innospec shares have added about 1.5% since the beginning of the year versus the S&P 500's gain of 7.6%.

What's Next for Innospec?While Innospec has underperformed the market so far this year, the question that comes to investors' minds is: what's next for the stock?

There are no easy answers to this key question, but one reliable measure that can help investors address this is the company's earnings outlook. Not only does this include current consensus earnings expectations for the coming quarter(s), but also how these expectations have changed lately.

Empirical research shows a strong correlation between near-term stock movements and trends in earnings estimate revisions. Investors can track such revisions by themselves or rely on a tried-and-tested rating tool like the Zacks Rank, which has an impressive track record of harnessing the power of earnings estimate revisions.

Ahead of this earnings release, the estimate revisions trend for Innospec was unfavorable. While the magnitude and direction of estimate revisions could change following the company's just-released earnings report, the current status translates into a Zacks Rank #4 (Sell) for the stock. So, the shares are expected to underperform the market in the near future. You can see the complete list of today's Zacks #1 Rank (Strong Buy) stocks here.

It will be interesting to see how estimates for the coming quarters and the current fiscal year change in the days ahead. The current consensus EPS estimate is $1.10 on $457.2 million in revenues for the coming quarter and $4.96 on $1.87 billion in revenues for the current fiscal year.

Investors should be mindful of the fact that the outlook for the industry can have a material impact on the performance of the stock as well. In terms of the Zacks Industry Rank, Chemical - Diversified is currently in the top 36% of the 250 plus Zacks industries. Our research shows that the top 50% of the Zacks-ranked industries outperform the bottom 50% by a factor of more than 2 to 1.

Another stock from the broader Zacks Basic Materials sector, Sylvamo Corporation (SLVM - Free Report) , has yet to report results for the quarter ended March 2026. The results are expected to be released on May 8.

This company is expected to post quarterly loss of $0.25 per share in its upcoming report, which represents a year-over-year change of -136.8%. The consensus EPS estimate for the quarter has been revised 4.6% higher over the last 30 days to the current level.

Sylvamo Corporation's revenues are expected to be $716 million, down 12.8% from the year-ago quarter.
2026-06-12 16:36 1mo ago
2026-05-08 15:21 2mo ago
Innospec Inc. (IOSP) Q1 2026 Earnings Call Transcript
IOSP Innospec
FMP Stock News
Original source text
Innospec Inc. (IOSP) Q1 2026 Earnings Call Transcript
2026-06-12 16:36 1mo ago
2026-05-08 16:05 2mo ago
Innospec Q1 Earnings Call Highlights
IOSP Innospec
FMP Stock News
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2026-06-12 16:36 1mo ago
2026-05-13 09:11 2mo ago
Innospec Q1 Earnings Beat Estimates, Sales Rise Y/Y On FX Tailwinds
IOSP Innospec
FMP Stock News
Original source text
Key Takeaways IOSP Q1 sales rose 3% to $453.2M, topping estimates despite lower adjusted EPS. Innospec raised its dividend 10% and announced a new $75M share repurchase plan. IOSP sees Q2 growth from plant repairs, pricing gains and Oilfield Services expansion. Innospec Inc. (IOSP - Free Report)  earnings per share (as reported) for the first quarter of 2026 declined to $1.22 per share from $1.31 a year ago.  

Adjusted earnings per share declined 26% to $1.05 per share from $1.42 a year ago. It beat the Zacks Consensus Estimate of $1.02 per share. 

Revenues for the first quarter rose 3% year over year to $453.2 million, beating the Zacks Consensus Estimate of $432.2 million. Adjusted EBITDA declined 19% year over year to $43.7 million. Operating income declined 14% to $36.5 million. 

Innospec Inc. Price, Consensus and EPS SurpriseSegment PerformanceFuel Specialties revenues rose 7% year over year to $181.6 million, driven by volume growth of 10% and a favorable currency impact of 6%, offset by an adverse price/mix of 9%. Gross margin compressed 0.3 percentage points to 35.4% and operating income increased 2% to $37.8 million.  

Performance Chemicals revenues rose 1% to $169.4 million as volume declines of 9% were offset by positive price/mix of 1% and favorable currency impact of 9%. Gross margin declined 4.2 percentage points to 16.8% and operating income fell 46% to $10.7 million, adversely impacted by shutdowns at the North Carolina plants due to the January 2026 U.S. winter storm. 

Oilfield Services revenues were essentially flat at $102.2 million. Gross margin improved 1.7 percentage points to 30.1% on a richer sales mix, and operating income increased 37% to $5.6 million, although results were also negatively impacted by the winter storm. 

FinancialsOperating cash flow was $17.6 million versus $28.3 million in the year-ago quarter. The company ended the quarter with cash of $289.1 million and no debt.

 In the first quarter, the effective tax rate was 22.8% compared with 25.7% in the year-ago quarter. The company increased its semi-annual dividend by 10% to 92 cents per share, repurchased $6.2 million of shares in the quarter and announced a new $75 million buyback authorization.

OutlookManagement expects sequential growth in the second quarter from Performance Chemicals, supported by plant repairs, pricing/mix opportunities and margin initiatives. 
For Oilfield Services, the company remains cautiously optimistic that recent DRA expansion and opportunities in completions and production will drive sequential improvement in the second quarter and position the business for further improvement in the second half of 2026. Fuel Specialties is expected to remain a stable contributor, with management citing continued strength across traditional fuel, renewable fuel and non-fuel applications. 

IOSP Stock’s Price PerformanceShares of Innospec have fallen 8.3% in the past year compared with the industry’s 18.7% growth.

Image Source: Zacks Investment Research

IOSP’s Zacks Rank & Key PicksIOSP currently sports a Zacks Rank #4 (Sell).

Some better-ranked stocks worth a look in the basic materials space are Sociedad Quimica y Minera de Chile S.A. (SQM - Free Report) , Idaho Strategic Resources, Inc. (IDR - Free Report) and NioCorp Developments Ltd. (NB - Free Report) .

Sociedad is slated to report first-quarter 2026 results on May 26. The Zacks Consensus Estimate for loss is pegged at $1.78 per share, indicating 270.8% year-over-year growth. SQM has a Zacks Rank #2 (Buy) at present.

Idaho is expected to report first-quarter 2026 results on May 14. The Zacks Consensus Estimate for earnings is pegged at 43 cents per share, indicating 258.3% year-over-year growth. IDR sports a Zacks Rank #1 (Strong Buy) at present. You can see the complete list of today’s Zacks #1 Rank stocks here.

NioCorp is expected to report fiscal third-quarter results on May 14. The Zacks Consensus Estimate for NB’s third-quarter loss is pegged at 2 cents per share. NB currently has a Zacks Rank #2.
2026-06-12 16:36 1mo ago
2026-04-07 03:30 3mo ago
Lincoln Electric Holdings, Inc. $LECO Shares Purchased by Azzad Asset Management Inc. ADV
LECO Lincoln Electric Holdings
FMP Stock News
Original source text
Posted by Defense World Staff on Apr 7th, 2026

Azzad Asset Management Inc. ADV grew its holdings in shares of Lincoln Electric Holdings, Inc. (NASDAQ:LECO – Free Report) by 37.3% during the fourth quarter, according to the company in its most recent filing with the Securities & Exchange Commission. The firm owned 15,901 shares of the industrial products company’s stock after purchasing an additional 4,317 shares during the quarter. Azzad Asset Management Inc. ADV’s holdings in Lincoln Electric were worth $3,811,000 at the end of the most recent quarter.

Other large investors also recently made changes to their positions in the company. Quent Capital LLC purchased a new position in shares of Lincoln Electric during the 3rd quarter worth $27,000. Frazier Financial Advisors LLC lifted its stake in shares of Lincoln Electric by 3,700.0% during the 3rd quarter. Frazier Financial Advisors LLC now owns 114 shares of the industrial products company’s stock worth $27,000 after purchasing an additional 111 shares during the period. Root Financial Partners LLC purchased a new position in shares of Lincoln Electric during the 3rd quarter worth $31,000. SJS Investment Consulting Inc. lifted its stake in shares of Lincoln Electric by 3,860.0% during the 3rd quarter. SJS Investment Consulting Inc. now owns 198 shares of the industrial products company’s stock worth $47,000 after purchasing an additional 193 shares during the period. Finally, Eastern Bank lifted its stake in shares of Lincoln Electric by 109.4% during the 3rd quarter. Eastern Bank now owns 201 shares of the industrial products company’s stock worth $47,000 after purchasing an additional 105 shares during the period. Hedge funds and other institutional investors own 79.61% of the company’s stock.

Lincoln Electric Trading Down 2.3% Shares of LECO opened at $238.05 on Tuesday. The company has a current ratio of 1.82, a quick ratio of 1.16 and a debt-to-equity ratio of 0.78. The firm has a market capitalization of $13.05 billion, a P/E ratio of 25.54, a price-to-earnings-growth ratio of 1.51 and a beta of 1.28. The stock’s fifty day simple moving average is $270.38 and its 200 day simple moving average is $250.86. Lincoln Electric Holdings, Inc. has a twelve month low of $161.11 and a twelve month high of $310.00.

Lincoln Electric (NASDAQ:LECO – Get Free Report) last issued its earnings results on Thursday, February 12th. The industrial products company reported $2.65 earnings per share for the quarter, topping the consensus estimate of $2.53 by $0.12. The business had revenue of $1.08 billion for the quarter, compared to analyst estimates of $1.09 billion. Lincoln Electric had a return on equity of 39.35% and a net margin of 12.30%.The business’s quarterly revenue was up 5.5% on a year-over-year basis. During the same period last year, the company posted $2.57 EPS. On average, equities research analysts forecast that Lincoln Electric Holdings, Inc. will post 9.36 earnings per share for the current year.

Lincoln Electric Announces Dividend The company also recently announced a quarterly dividend, which will be paid on Wednesday, April 15th. Investors of record on Tuesday, March 31st will be given a $0.79 dividend. This represents a $3.16 annualized dividend and a dividend yield of 1.3%. The ex-dividend date of this dividend is Tuesday, March 31st. Lincoln Electric’s dividend payout ratio (DPR) is 33.91%.

Wall Street Analyst Weigh In LECO has been the topic of a number of recent analyst reports. Wall Street Zen lowered Lincoln Electric from a “buy” rating to a “hold” rating in a research note on Saturday, February 28th. Weiss Ratings lowered Lincoln Electric from a “buy (b-)” rating to a “hold (c+)” rating in a research note on Tuesday, March 31st. Barclays reduced their price target on Lincoln Electric from $310.00 to $280.00 and set an “overweight” rating on the stock in a research note on Wednesday, April 1st. Stifel Nicolaus increased their price target on Lincoln Electric from $253.00 to $300.00 and gave the stock a “hold” rating in a research note on Friday, February 13th. Finally, Roth Mkm reissued a “buy” rating and set a $297.00 price target (up from $285.00) on shares of Lincoln Electric in a research note on Tuesday, February 3rd. Four research analysts have rated the stock with a Buy rating, four have given a Hold rating and one has assigned a Sell rating to the company’s stock. According to MarketBeat.com, Lincoln Electric presently has a consensus rating of “Hold” and an average price target of $296.29.

Get Our Latest Analysis on LECO

Lincoln Electric Profile (Free Report)

Lincoln Electric Holdings, Inc (NASDAQ: LECO) is a global manufacturer and distributor of welding products, robotic welding systems, plasma and oxyfuel cutting equipment, and surface treatment systems. The company’s portfolio encompasses welding consumables such as electrodes and wires, as well as power sources, torches, and automated welding cells. Lincoln Electric also offers software solutions and training services designed to optimize productivity and quality in fabrication and manufacturing operations.

Founded in 1895 by John C.

Featured Articles Five stocks we like better than Lincoln Electric Want to see what other hedge funds are holding LECO? Visit HoldingsChannel.com to get the latest 13F filings and insider trades for Lincoln Electric Holdings, Inc. (NASDAQ:LECO – Free Report).

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2026-06-12 16:36 1mo ago
2026-04-11 04:18 3mo ago
Carnegie Investment Counsel Buys 59,619 Shares of Lincoln Electric Holdings, Inc. $LECO
LECO Lincoln Electric Holdings
FMP Stock News
Original source text
Posted by Defense World Staff on Apr 11th, 2026

Carnegie Investment Counsel raised its stake in Lincoln Electric Holdings, Inc. (NASDAQ:LECO – Free Report) by 293.1% in the fourth quarter, according to the company in its most recent disclosure with the Securities & Exchange Commission. The institutional investor owned 79,958 shares of the industrial products company’s stock after purchasing an additional 59,619 shares during the quarter. Carnegie Investment Counsel owned approximately 0.15% of Lincoln Electric worth $19,161,000 at the end of the most recent reporting period.

Other hedge funds have also recently bought and sold shares of the company. Victory Capital Management Inc. lifted its position in shares of Lincoln Electric by 4.1% in the third quarter. Victory Capital Management Inc. now owns 1,850,816 shares of the industrial products company’s stock valued at $436,478,000 after buying an additional 72,826 shares during the last quarter. Invesco Ltd. lifted its position in shares of Lincoln Electric by 31.8% in the third quarter. Invesco Ltd. now owns 919,926 shares of the industrial products company’s stock valued at $216,946,000 after buying an additional 221,853 shares during the last quarter. Boston Partners lifted its position in shares of Lincoln Electric by 24.6% in the third quarter. Boston Partners now owns 850,201 shares of the industrial products company’s stock valued at $200,517,000 after buying an additional 167,773 shares during the last quarter. AQR Capital Management LLC lifted its position in shares of Lincoln Electric by 21.8% in the third quarter. AQR Capital Management LLC now owns 726,949 shares of the industrial products company’s stock valued at $171,167,000 after buying an additional 130,332 shares during the last quarter. Finally, MIRAE ASSET GLOBAL ETFS HOLDINGS Ltd. lifted its position in shares of Lincoln Electric by 1.5% in the third quarter. MIRAE ASSET GLOBAL ETFS HOLDINGS Ltd. now owns 375,068 shares of the industrial products company’s stock valued at $88,452,000 after buying an additional 5,365 shares during the last quarter. 79.61% of the stock is currently owned by institutional investors.

Analysts Set New Price Targets A number of analysts have recently issued reports on LECO shares. Wall Street Zen cut Lincoln Electric from a “buy” rating to a “hold” rating in a research report on Saturday, February 28th. Barclays cut their price objective on Lincoln Electric from $310.00 to $280.00 and set an “overweight” rating for the company in a research report on Wednesday, April 1st. Robert W. Baird set a $330.00 price objective on Lincoln Electric in a research report on Friday, February 13th. Jefferies Financial Group reissued a “hold” rating and set a $280.00 price target (down from $350.00) on shares of Lincoln Electric in a report on Tuesday, March 31st. Finally, Roth Mkm reissued a “buy” rating and set a $297.00 price target (up from $285.00) on shares of Lincoln Electric in a report on Tuesday, February 3rd. Four investment analysts have rated the stock with a Buy rating, four have issued a Hold rating and one has issued a Sell rating to the stock. According to MarketBeat, the company presently has a consensus rating of “Hold” and a consensus target price of $291.14.

Read Our Latest Stock Analysis on Lincoln Electric

Lincoln Electric Stock Performance NASDAQ:LECO opened at $256.26 on Friday. The stock has a market cap of $14.05 billion, a P/E ratio of 27.50, a PEG ratio of 1.59 and a beta of 1.28. The stock has a 50 day simple moving average of $269.62 and a 200 day simple moving average of $251.07. The company has a current ratio of 1.82, a quick ratio of 1.16 and a debt-to-equity ratio of 0.78. Lincoln Electric Holdings, Inc. has a 1-year low of $169.69 and a 1-year high of $310.00.

Lincoln Electric (NASDAQ:LECO – Get Free Report) last released its quarterly earnings results on Thursday, February 12th. The industrial products company reported $2.65 earnings per share for the quarter, topping the consensus estimate of $2.53 by $0.12. The business had revenue of $1.08 billion during the quarter, compared to analysts’ expectations of $1.09 billion. Lincoln Electric had a return on equity of 39.35% and a net margin of 12.30%.The firm’s revenue for the quarter was up 5.5% compared to the same quarter last year. During the same period last year, the firm posted $2.57 EPS. Research analysts anticipate that Lincoln Electric Holdings, Inc. will post 9.36 earnings per share for the current year.

Lincoln Electric Dividend Announcement The business also recently disclosed a quarterly dividend, which will be paid on Wednesday, April 15th. Shareholders of record on Tuesday, March 31st will be issued a $0.79 dividend. The ex-dividend date of this dividend is Tuesday, March 31st. This represents a $3.16 annualized dividend and a yield of 1.2%. Lincoln Electric’s payout ratio is currently 33.91%.

Lincoln Electric Profile (Free Report)

Lincoln Electric Holdings, Inc (NASDAQ: LECO) is a global manufacturer and distributor of welding products, robotic welding systems, plasma and oxyfuel cutting equipment, and surface treatment systems. The company’s portfolio encompasses welding consumables such as electrodes and wires, as well as power sources, torches, and automated welding cells. Lincoln Electric also offers software solutions and training services designed to optimize productivity and quality in fabrication and manufacturing operations.

Founded in 1895 by John C.

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2026-06-12 16:36 1mo ago
2026-04-13 12:40 3mo ago
KMT or LECO: Which Is the Better Value Stock Right Now?
LECO Lincoln Electric Holdings
FMP Stock News
Original source text
Investors interested in stocks from the Manufacturing - Tools & Related Products sector have probably already heard of Kennametal (KMT) and Lincoln Electric Holdings (LECO). But which of these two stocks offers value investors a better bang for their buck right now?
2026-06-12 16:36 1mo ago
2026-04-14 04:30 3mo ago
Deprince Race & Zollo Inc. Trims Holdings in Lincoln Electric Holdings, Inc. $LECO
LECO Lincoln Electric Holdings
FMP Stock News
Original source text
Posted by Defense World Staff on Apr 14th, 2026

Deprince Race & Zollo Inc. trimmed its position in Lincoln Electric Holdings, Inc. (NASDAQ:LECO – Free Report) by 21.6% in the 4th quarter, according to the company in its most recent disclosure with the Securities & Exchange Commission. The fund owned 38,462 shares of the industrial products company’s stock after selling 10,614 shares during the quarter. Deprince Race & Zollo Inc. owned about 0.07% of Lincoln Electric worth $9,217,000 as of its most recent SEC filing.

Several other institutional investors have also recently modified their holdings of the company. Burney Co. purchased a new position in shares of Lincoln Electric in the fourth quarter worth about $223,000. Choreo LLC raised its stake in shares of Lincoln Electric by 11.7% in the fourth quarter. Choreo LLC now owns 3,097 shares of the industrial products company’s stock worth $754,000 after purchasing an additional 324 shares during the last quarter. Ritholtz Wealth Management raised its stake in shares of Lincoln Electric by 19.9% in the fourth quarter. Ritholtz Wealth Management now owns 1,327 shares of the industrial products company’s stock worth $318,000 after purchasing an additional 220 shares during the last quarter. Diversify Advisory Services LLC raised its stake in shares of Lincoln Electric by 11.3% in the fourth quarter. Diversify Advisory Services LLC now owns 1,913 shares of the industrial products company’s stock worth $504,000 after purchasing an additional 194 shares during the last quarter. Finally, Carnegie Investment Counsel raised its stake in shares of Lincoln Electric by 293.1% in the fourth quarter. Carnegie Investment Counsel now owns 79,958 shares of the industrial products company’s stock worth $19,161,000 after purchasing an additional 59,619 shares during the last quarter. 79.61% of the stock is currently owned by hedge funds and other institutional investors.

Analyst Ratings Changes Several brokerages have recently issued reports on LECO. KeyCorp raised their price objective on Lincoln Electric from $280.00 to $340.00 and gave the stock an “overweight” rating in a research note on Friday, February 13th. Weiss Ratings cut Lincoln Electric from a “buy (b-)” rating to a “hold (c+)” rating in a research note on Tuesday, March 31st. Robert W. Baird set a $330.00 price objective on Lincoln Electric in a research note on Friday, February 13th. Stifel Nicolaus dropped their target price on Lincoln Electric from $300.00 to $264.00 and set a “hold” rating on the stock in a report on Wednesday, April 8th. Finally, Morgan Stanley lifted their price target on Lincoln Electric from $240.00 to $247.00 and gave the company an “underweight” rating in a research report on Monday, March 30th. Four equities research analysts have rated the stock with a Buy rating, four have given a Hold rating and one has given a Sell rating to the stock. Based on data from MarketBeat.com, the company has an average rating of “Hold” and a consensus target price of $291.14.

Read Our Latest Report on LECO

Lincoln Electric Stock Up 1.5% Lincoln Electric stock opened at $260.15 on Tuesday. The stock has a market capitalization of $14.26 billion, a PE ratio of 27.91, a price-to-earnings-growth ratio of 1.59 and a beta of 1.28. Lincoln Electric Holdings, Inc. has a 12 month low of $169.69 and a 12 month high of $310.00. The business has a 50 day simple moving average of $269.47 and a 200-day simple moving average of $251.46. The company has a debt-to-equity ratio of 0.78, a current ratio of 1.82 and a quick ratio of 1.16.

Lincoln Electric (NASDAQ:LECO – Get Free Report) last issued its quarterly earnings results on Thursday, February 12th. The industrial products company reported $2.65 earnings per share (EPS) for the quarter, topping analysts’ consensus estimates of $2.53 by $0.12. The firm had revenue of $1.08 billion for the quarter, compared to analyst estimates of $1.09 billion. Lincoln Electric had a return on equity of 39.35% and a net margin of 12.30%.The business’s revenue was up 5.5% on a year-over-year basis. During the same period in the previous year, the company posted $2.57 earnings per share. On average, analysts anticipate that Lincoln Electric Holdings, Inc. will post 9.36 EPS for the current fiscal year.

Lincoln Electric Dividend Announcement The business also recently disclosed a quarterly dividend, which will be paid on Wednesday, April 15th. Shareholders of record on Tuesday, March 31st will be paid a dividend of $0.79 per share. The ex-dividend date of this dividend is Tuesday, March 31st. This represents a $3.16 dividend on an annualized basis and a yield of 1.2%. Lincoln Electric’s payout ratio is 33.91%.

Lincoln Electric Profile (Free Report)

Lincoln Electric Holdings, Inc (NASDAQ: LECO) is a global manufacturer and distributor of welding products, robotic welding systems, plasma and oxyfuel cutting equipment, and surface treatment systems. The company’s portfolio encompasses welding consumables such as electrodes and wires, as well as power sources, torches, and automated welding cells. Lincoln Electric also offers software solutions and training services designed to optimize productivity and quality in fabrication and manufacturing operations.

Founded in 1895 by John C.

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