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2026-06-12 15:51 2mo ago
2026-05-06 08:19 4mo ago
Strong Q2 Portends Continued Success For New Jersey Resources
NJR NewJersey Resources Corporation
FMP Stock News
Original source text
New Jersey Resources is executing a clean energy pivot, allocating over 60% of $4.8–$5.2 billion CapEx through FY2030 to solar-focused Clean Energy Ventures. NJR delivered strong winter-driven Q2 results, beating non-GAAP EPS by $0.30 and revenue by nearly 10%, and raised full-year non-GAAP EPS guidance to $3.48–$3.62. Despite robust operating cash flow growth, NJR's high CapEx outpaces cash generation, requiring increased debt while targeting a 20% adjusted debt-to-capital ratio.
2026-06-12 15:51 2mo ago
2026-05-11 16:05 4mo ago
New Jersey Natural Gas Names Helen Ayotte Vice President of Engineering, Construction and Asset Management
NJR NewJersey Resources Corporation
FMP Stock News
Original source text
WALL, N.J.--(BUSINESS WIRE)--New Jersey Natural Gas, (NJNG), a regulated subsidiary of New Jersey Resources (NYSE: NJR), announced the appointment of Helen Ayotte as Vice President of Engineering, Construction and Asset Management effective today. Ms. Ayotte will succeed John Wyckoff, Vice President of Energy Delivery, who is retiring on July 1, 2026. In this role, Ms. Ayotte will oversee NJNG's engineering, construction, environmental and asset management functions, ensuring the safe and relia.
2026-06-12 15:51 2mo ago
2026-05-15 10:16 3mo ago
NewJersey Resources Corporation (NJR) Hit a 52 Week High, Can the Run Continue?
NJR NewJersey Resources Corporation
FMP Stock News
Original source text
A strong stock as of late has been New Jersey Resources (NJR - Free Report) . Shares have been marching higher, with the stock up 3.3% over the past month. The stock hit a new 52-week high of $57.91 in the previous session. New Jersey Resources has gained 25.3% since the start of the year compared to the 6.9% move for the Zacks Utilities sector and the 5.8% return for the Zacks Utility - Gas Distribution industry.

What's Driving the Outperformance?The stock has a great record of positive earnings surprises, having beaten the Zacks Consensus Estimate in each of the last four quarters. In its last earnings report on May 4, 2026, New Jersey Resources reported EPS of $2.2 versus consensus estimate of $1.89.

For the current fiscal year, New Jersey Resources is expected to post earnings of $3.45 per share on $2.21 in revenues. This represents a 5.5% change in EPS on a 8.54% change in revenues. For the next fiscal year, the company is expected to earn $3.47 per share on $2.36 in revenues. This represents a year-over-year change of 0.65% and 6.56%, respectively.

Valuation MetricsWhile New Jersey Resources has moved to its 52-week high over the past few weeks, investors need to be asking, what is next for the company? A key aspect of this question is taking a look at valuation metrics in order to determine if the company is due for a pullback from this level.

On this front, we can look at the Zacks Style Scores, as they provide investors with an additional way to sort through stocks (beyond looking at the Zacks Rank of a security). These styles are represented by grades running from A to F in the categories of Value, Growth, and Momentum, while there is a combined VGM Score as well. The idea behind the style scores is to help investors pick the most appropriate Zacks Rank stocks based on their individual investment style.

New Jersey Resources has a Value Score of B. The stock's Growth and Momentum Scores are B and B, respectively, giving the company a VGM Score of B.

In terms of its value breakdown, the stock currently trades at 16.8X current fiscal year EPS estimates, which is not in-line with the peer industry average of 17.6X. On a trailing cash flow basis, the stock currently trades at 11.2X versus its peer group's average of 9.4X. This isn't enough to put the company in the top echelon of all stocks we cover from a value perspective.

Zacks RankWe also need to consider the stock's Zacks Rank, as this supersedes any trend on the style score front. Fortunately, New Jersey Resources currently has a Zacks Rank of #2 (Buy) thanks to a solid earnings estimate revision trend.

Since we recommend that investors select stocks carrying Zacks Rank of 1 (Strong Buy) or 2 (Buy) and Style Scores of A or B, it looks as if New Jersey Resources fits the bill. Thus, it seems as though New Jersey Resources shares could have potential in the weeks and months to come.
2026-06-12 15:51 2mo ago
2026-05-18 12:47 3mo ago
New Jersey Resources (NJR) Could Be a Great Choice
NJR NewJersey Resources Corporation
FMP Stock News
Original source text
Getting big returns from financial portfolios, whether through stocks, bonds, ETFs, other securities, or a combination of all, is an investor's dream. But for income investors, generating consistent cash flow from each of your liquid investments is your primary focus.

While cash flow can come from bond interest or interest from other types of investments, income investors hone in on dividends. A dividend is the distribution of a company's earnings paid out to shareholders; it's often viewed by its dividend yield, a metric that measures a dividend as a percent of the current stock price. Many academic studies show that dividends make up large portions of long-term returns, and in many cases, dividend contributions surpass one-third of total returns.

New Jersey Resources (NJR - Free Report) is headquartered in Wall, and is in the Utilities sector. The stock has seen a price change of 24.31% since the start of the year. The energy services holding company is currently shelling out a dividend of $0.47 per share, with a dividend yield of 3.31%. This compares to the Utility - Gas Distribution industry's yield of 3.08% and the S&P 500's yield of 1.45%.

Looking at dividend growth, the company's current annualized dividend of $1.90 is up 4.1% from last year. Over the last 5 years, New Jersey Resources has increased its dividend 5 times on a year-over-year basis for an average annual increase of 7.51%. Looking ahead, future dividend growth will be dependent on earnings growth and payout ratio, which is the proportion of a company's annual earnings per share that it pays out as a dividend. New Jersey Resources's current payout ratio is 53%, meaning it paid out 53% of its trailing 12-month EPS as dividend.

Earnings growth looks solid for NJR for this fiscal year. The Zacks Consensus Estimate for 2026 is $3.45 per share, representing a year-over-year earnings growth rate of 5.50%.

From greatly improving stock investing profits and reducing overall portfolio risk to providing tax advantages, investors like dividends for a variety of different reasons. However, not all companies offer a quarterly payout.

High-growth firms or tech start-ups, for example, rarely provide their shareholders a dividend, while larger, more established companies that have more secure profits are often seen as the best dividend options. Income investors have to be mindful of the fact that high-yielding stocks tend to struggle during periods of rising interest rates. With that in mind, NJR presents a compelling investment opportunity; it's not only an attractive dividend play, but the stock also boasts a strong Zacks Rank of #2 (Buy).
2026-06-12 15:51 2mo ago
2026-05-19 10:41 3mo ago
Is NewJersey Resources (NJR) Stock Outpacing Its Utilities Peers This Year?
NJR NewJersey Resources Corporation
FMP Stock News
Original source text
The Utilities group has plenty of great stocks, but investors should always be looking for companies that are outperforming their peers. New Jersey Resources (NJR - Free Report) is a stock that can certainly grab the attention of many investors, but do its recent returns compare favorably to the sector as a whole? Let's take a closer look at the stock's year-to-date performance to find out.

New Jersey Resources is a member of our Utilities group, which includes 110 different companies and currently sits at #14 in the Zacks Sector Rank. The Zacks Sector Rank includes 16 different groups and is listed in order from best to worst in terms of the average Zacks Rank of the individual companies within each of these sectors.

The Zacks Rank is a proven system that emphasizes earnings estimates and estimate revisions, highlighting a variety of stocks that are displaying the right characteristics to beat the market over the next one to three months. New Jersey Resources is currently sporting a Zacks Rank of #2 (Buy).

Over the past 90 days, the Zacks Consensus Estimate for NJR's full-year earnings has moved 4% higher. This means that analyst sentiment is stronger and the stock's earnings outlook is improving.

Based on the latest available data, NJR has gained about 24.9% so far this year. In comparison, Utilities companies have returned an average of 4.8%. This means that New Jersey Resources is outperforming the sector as a whole this year.

One other Utilities stock that has outperformed the sector so far this year is Sabesp (SBS - Free Report) . The stock is up 22.6% year-to-date.

The consensus estimate for Sabesp's current year EPS has increased 322.9% over the past three months. The stock currently has a Zacks Rank #2 (Buy).

Looking more specifically, New Jersey Resources belongs to the Utility - Gas Distribution industry, which includes 13 individual stocks and currently sits at #180 in the Zacks Industry Rank. Stocks in this group have gained about 5.3% so far this year, so NJR is performing better this group in terms of year-to-date returns.

On the other hand, Sabesp belongs to the Utility - Water Supply industry. This 11-stock industry is currently ranked #185. The industry has moved +3.7% year to date.

New Jersey Resources and Sabesp could continue their solid performance, so investors interested in Utilities stocks should continue to pay close attention to these stocks.
2026-06-12 15:51 2mo ago
2026-05-20 13:45 3mo ago
Is New Jersey Resources (NJR) a Solid Growth Stock? 3 Reasons to Think "Yes"
NJR NewJersey Resources Corporation
FMP Stock News
Original source text
Growth investors focus on stocks that are seeing above-average financial growth, as this feature helps these securities garner the market's attention and deliver solid returns. However, it isn't easy to find a great growth stock.

By their very nature, these stocks carry above-average risk and volatility. Moreover, if a company's growth story is over or nearing its end, betting on it could lead to significant loss.

However, the task of finding cutting-edge growth stocks is made easy with the help of the Zacks Growth Style Score (part of the Zacks Style Scores system), which looks beyond the traditional growth attributes to analyze a company's real growth prospects.

New Jersey Resources (NJR - Free Report) is one such stock that our proprietary system currently recommends. The company not only has a favorable Growth Score, but also carries a top Zacks Rank.

Studies have shown that stocks with the best growth features consistently outperform the market. And returns are even better for stocks that possess the combination of a Growth Score of A or B and a Zacks Rank #1 (Strong Buy) or 2 (Buy).

Here are three of the most important factors that make the stock of this energy services holding company a great growth pick right now.

Earnings GrowthEarnings growth is arguably the most important factor, as stocks exhibiting exceptionally surging profit levels tend to attract the attention of most investors. For growth investors, double-digit earnings growth is highly preferable, as it is often perceived as an indication of strong prospects (and stock price gains) for the company under consideration.

While the historical EPS growth rate for New Jersey Resources is 11%, investors should actually focus on the projected growth. The company's EPS is expected to grow 5.4% this year, crushing the industry average, which calls for EPS growth of 5.2%.

Cash Flow GrowthWhile cash is the lifeblood of any business, higher-than-average cash flow growth is more important and beneficial for growth-oriented companies than for mature companies. That's because, growth in cash flow enables these companies to expand their businesses without depending on expensive outside funds.

Right now, year-over-year cash flow growth for New Jersey Resources is 13.3%, which is higher than many of its peers. In fact, the rate compares to the industry average of 12%.

While investors should actually consider the current cash flow growth, it's worth taking a look at the historical rate too for putting the current reading into proper perspective. The company's annualized cash flow growth rate has been 11.3% over the past 3-5 years versus the industry average of 7%.

Promising Earnings Estimate RevisionsBeyond the metrics outlined above, investors should consider the trend in earnings estimate revisions. A positive trend is a plus here. Empirical research shows that there is a strong correlation between trends in earnings estimate revisions and near-term stock price movements.

There have been upward revisions in current-year earnings estimates for New Jersey Resources. The Zacks Consensus Estimate for the current year has surged 5.7% over the past month.

Bottom LineNew Jersey Resources has not only earned a Growth Score of B based on a number of factors, including the ones discussed above, but it also carries a Zacks Rank #2 because of the positive earnings estimate revisions.

You can see the complete list of today's Zacks #1 Rank (Strong Buy) stocks here.

This combination indicates that New Jersey Resources is a potential outperformer and a solid choice for growth investors.
2026-06-12 15:51 2mo ago
2026-06-01 16:05 3mo ago
New Jersey Natural Gas Submits Filings to NJBPU for Customer Savings and Future Recovery of Reliability Investments
NJR NewJersey Resources Corporation
FMP Stock News
Original source text
WALL, N.J.--(BUSINESS WIRE)--New Jersey Natural Gas (NJNG), the principal subsidiary of New Jersey Resources (NYSE: NJR), today announced it has submitted filings to the New Jersey Board of Public Utilities (NJBPU) that, taken together, provide customers with a 8.9% reduction in customer bills in advance of the 2026-2027 winter season – a $158 annual savings for the average residential customer – and rate stability while seeking recovery for investments in the continued delivery of safe, reliab.
2026-06-12 15:51 2mo ago
2026-04-22 08:00 4mo ago
Madrigal Pharmaceuticals to Release First-Quarter 2026 Financial Results and Host Webcast on May 6, 2026
MDGL Madrigal Pharmaceuticals
FMP Stock News
Original source text
CONSHOHOCKEN, Pa., April 22, 2026 (GLOBE NEWSWIRE) -- Madrigal Pharmaceuticals, Inc. (Nasdaq: MDGL) announced today that it will release its first-quarter 2026 financial results on Wednesday, May 6, 2026, prior to the open of the U.S. financial markets.

Following the announcement, Madrigal’s management will host a live webcast at 8 a.m. Eastern Time to review the Company’s financial and operating results.

The live webcast may be accessed at the Investor Relations section of the Madrigal Pharmaceuticals website. To ensure a timely connection, it is recommended that participants register at least 15 minutes prior to the scheduled webcast.

The webcast will be available approximately two hours after the live webcast.

About Madrigal Pharmaceuticals
Madrigal Pharmaceuticals, Inc. (Nasdaq: MDGL) is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a liver disease with high unmet medical need. Madrigal’s medication, Rezdiffra (resmetirom), is a once-daily, oral, liver-directed THR-β agonist designed to target key underlying causes of MASH. Rezdiffra is the first and only medication approved by both the FDA and European Commission for the treatment of MASH with moderate to advanced fibrosis (F2 to F3). An ongoing Phase 3 outcomes trial is evaluating Rezdiffra for the treatment of compensated MASH cirrhosis (F4c). For more information, visit www.madrigalpharma.com.

Investor Contact
Tina Ventura, Madrigal Pharmaceuticals, Inc., [email protected]

Media Contact
Christopher Frates, Madrigal Pharmaceuticals, Inc., [email protected]
2026-06-12 15:51 2mo ago
2026-04-27 02:38 4mo ago
Madrigal Pharmaceuticals, Inc. (NASDAQ:MDGL) Receives Consensus Recommendation of “Moderate Buy” from Brokerages
MDGL Madrigal Pharmaceuticals
FMP Stock News
Original source text
Posted by Defense World Staff on Apr 27th, 2026

Madrigal Pharmaceuticals, Inc. (NASDAQ:MDGL – Get Free Report) has received an average rating of “Moderate Buy” from the seventeen ratings firms that are presently covering the company, Marketbeat.com reports. One investment analyst has rated the stock with a sell rating, three have given a hold rating, twelve have issued a buy rating and one has issued a strong buy rating on the company. The average 12-month price objective among analysts that have issued a report on the stock in the last year is $685.3077.

Several brokerages have commented on MDGL. Wolfe Research set a $579.00 price objective on shares of Madrigal Pharmaceuticals in a report on Tuesday, January 6th. The Goldman Sachs Group reiterated a “buy” rating and set a $571.00 target price on shares of Madrigal Pharmaceuticals in a report on Wednesday, January 14th. Citigroup reissued an “outperform” rating on shares of Madrigal Pharmaceuticals in a research report on Tuesday, January 20th. Zacks Research upgraded Madrigal Pharmaceuticals from a “strong sell” rating to a “hold” rating in a research note on Friday, February 20th. Finally, Bank of America dropped their price target on Madrigal Pharmaceuticals from $570.00 to $529.00 and set a “neutral” rating on the stock in a research report on Friday, February 20th.

View Our Latest Research Report on Madrigal Pharmaceuticals

Madrigal Pharmaceuticals Stock Performance NASDAQ:MDGL opened at $512.39 on Monday. The company has a quick ratio of 3.77, a current ratio of 4.01 and a debt-to-equity ratio of 0.56. Madrigal Pharmaceuticals has a 52 week low of $265.00 and a 52 week high of $615.00. The firm has a market capitalization of $11.75 billion, a P/E ratio of -39.81 and a beta of -1.00. The company has a fifty day moving average of $479.28 and a 200 day moving average of $502.84.

Madrigal Pharmaceuticals (NASDAQ:MDGL – Get Free Report) last posted its earnings results on Thursday, February 19th. The biopharmaceutical company reported ($2.57) EPS for the quarter, missing the consensus estimate of $0.04 by ($2.61). Madrigal Pharmaceuticals had a negative return on equity of 43.76% and a negative net margin of 30.08%.The company had revenue of $321.08 million during the quarter, compared to analysts’ expectations of $310.36 million. During the same period in the prior year, the business posted ($2.71) earnings per share. The company’s revenue for the quarter was up 210.8% on a year-over-year basis. On average, research analysts predict that Madrigal Pharmaceuticals will post -5.22 earnings per share for the current year.

Insider Buying and Selling at Madrigal Pharmaceuticals In other Madrigal Pharmaceuticals news, General Counsel Shannon T. Kelley sold 360 shares of the firm’s stock in a transaction on Friday, March 6th. The stock was sold at an average price of $431.94, for a total transaction of $155,498.40. Following the completion of the transaction, the general counsel owned 12,138 shares of the company’s stock, valued at approximately $5,242,887.72. This trade represents a 2.88% decrease in their ownership of the stock. The sale was disclosed in a filing with the SEC, which can be accessed through this link. Also, CEO William John Sibold sold 1,663 shares of the company’s stock in a transaction dated Friday, March 6th. The stock was sold at an average price of $431.94, for a total transaction of $718,316.22. Following the completion of the sale, the chief executive officer directly owned 161,829 shares in the company, valued at $69,900,418.26. This represents a 1.02% decrease in their ownership of the stock. The SEC filing for this sale provides additional information. In the last three months, insiders have sold 6,098 shares of company stock valued at $2,626,254. Company insiders own 21.50% of the company’s stock.

Institutional Investors Weigh In On Madrigal Pharmaceuticals A number of hedge funds and other institutional investors have recently bought and sold shares of MDGL. Flagship Harbor Advisors LLC purchased a new position in shares of Madrigal Pharmaceuticals during the fourth quarter valued at approximately $29,000. Aventura Private Wealth LLC bought a new stake in shares of Madrigal Pharmaceuticals in the 4th quarter worth approximately $36,000. Kemnay Advisory Services Inc. purchased a new stake in shares of Madrigal Pharmaceuticals in the 4th quarter worth approximately $39,000. Mather Group LLC. bought a new position in Madrigal Pharmaceuticals during the 3rd quarter valued at approximately $33,000. Finally, Global Retirement Partners LLC increased its position in Madrigal Pharmaceuticals by 221.7% during the 3rd quarter. Global Retirement Partners LLC now owns 74 shares of the biopharmaceutical company’s stock valued at $34,000 after buying an additional 51 shares in the last quarter. Hedge funds and other institutional investors own 98.50% of the company’s stock.

Madrigal Pharmaceuticals Company Profile (Get Free Report)

Madrigal Pharmaceuticals, Inc is a clinical-stage biopharmaceutical company focused on the development of innovative therapies for cardiovascular, metabolic and liver diseases. The company’s pipeline centers on novel, liver-directed agents designed to address significant unmet medical needs, with an emphasis on nonalcoholic steatohepatitis (NASH) and related metabolic disorders.

The lead product candidate, resmetirom (MGL-3196), is an orally administered, selective thyroid hormone receptor-β agonist in Phase 3 development for the treatment of NASH.

See Also Five stocks we like better than Madrigal Pharmaceuticals

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2026-06-12 15:51 2mo ago
2026-04-28 14:27 4mo ago
Madrigal Pharmaceuticals: Boom Or Bust In MASH? Regretfully, I'm Bearish
MDGL Madrigal Pharmaceuticals
FMP Stock News
Original source text
Madrigal Pharmaceuticals, Inc. receives a Sell rating, citing high valuation and intensifying MASH competition despite Rezdiffra's initial commercial success. Rezdiffra achieved $958.4m in 2025 sales with ~36,250 patients, but MDGL profitability remains elusive as operating expenses outpace revenue growth. SG&A and R&D costs are expected to rise in 2026, while no specific guidance has been provided, and consensus sees potential Q1 revenue softness.
2026-06-12 15:51 2mo ago
2026-04-30 11:06 4mo ago
Analysts Estimate Crinetics Pharmaceuticals, Inc. (CRNX) to Report a Decline in Earnings: What to Look Out for
MDGL Madrigal Pharmaceuticals
FMP Stock News
Original source text
The market expects Crinetics Pharmaceuticals, Inc. (CRNX - Free Report) to deliver a year-over-year decline 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 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 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 loss of $1.22 per share in its upcoming report, which represents a year-over-year change of -17.3%.

Revenues are expected to be $7.55 million, up 1997.2% from the year-ago quarter.

Estimate Revisions TrendThe consensus EPS estimate for the quarter has been revised 1.73% 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 CRINETICS PHARM?For CRINETICS PHARM, the Most Accurate Estimate is lower than the Zacks Consensus Estimate, suggesting that analysts have recently become bearish on the company's earnings prospects. This has resulted in an Earnings ESP of -9.02%.

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

So, this combination makes it difficult to conclusively predict that CRINETICS PHARM 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 CRINETICS PHARM would post a loss of$1.37 per share when it actually produced a loss of -$1.29, delivering a surprise of +5.84%.

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

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.

CRINETICS PHARM 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 ResultsAnother stock from the Zacks Medical - Drugs industry, Madrigal (MDGL - Free Report) , is soon expected to post loss of $3.28 per share for the quarter ended March 2026. This estimate indicates a year-over-year change of +1.2%. Revenues for the quarter are expected to be $301.15 million, up 119.4% from the year-ago quarter.

The consensus EPS estimate for Madrigal has been revised 2% higher over the last 30 days to the current level. However, a higher Most Accurate Estimate has resulted in an Earnings ESP of +61.01%.

When combined with a Zacks Rank of #3 (Hold), this Earnings ESP indicates that Madrigal will most likely 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 15:51 2mo ago
2026-05-03 09:30 4mo ago
3 Biotech Stocks to Watch for Respectable Growth Beyond AI
MDGL Madrigal Pharmaceuticals
FMP Stock News
Original source text
© gorodenkoff / Getty Images

Artificial intelligence has dominated investor attention for two years, but biotech revenue lines are also bending sharply higher. A small group of biotechs is building real commercial businesses around recently approved drugs, with growth profiles that stack up favorably against many AI darlings on a fundamentals basis. The three names below all reported Q4 2025 results in February, all have approved products generating meaningful revenue, and all carry catalysts that should drive the story through 2026 and beyond.

The screen is straightforward: an approved, commercially active drug; durable revenue growth in the most recent quarter; visible 2026 catalysts; and a multi-year runway that does not depend on a hyperscaler capex cycle.

1. Cytokinetics (CYTK) Cytokinetics (NASDAQ:CYTK | CYTK Price Prediction) is the most speculative of the three, but it just crossed the most important line in biotech. MYQORZO (aficamten) received FDA approval in December 2025, and the U.S. launch is underway. Q4 2025 revenue came in at $17.75 million, beating the $8.02 million consensus by 121%, driven by milestone payments under the Sanofi license agreement. EPS of -$1.50 missed the -$1.37 estimate as the company built out its commercial infrastructure.

The financial profile carries real risk. Shareholders’ equity sits at -$659.63 million, and 2026 guidance calls for combined GAAP R&D and SG&A of $830 million to $870 million. The offset is a calendar of catalysts: ACACIA-HCM topline results in Q2 2026, a German MYQORZO launch in Q2, and a potential MAPLE-HCM sNDA approval in Q4 2026. CEO Robert Blum called the quarter “a defining moment” for the company’s transition to commercial stage. Wall Street agrees, with an analyst target of $92.94 against a recent price near $62.29. Shares are up 44% over the past year.

2. Madrigal Pharmaceuticals (MDGL) Madrigal Pharmaceuticals (NASDAQ:MDGL) is running one of the most successful specialty launches in recent memory. Rezdiffra, the first approved MASH therapy, posted Q4 2025 net sales of $321.10 million, up 211% year over year, and full-year 2025 revenue of $958.40 million versus $180.10 million in 2024, growth of 432%. The patient base climbed from 17,000 in Q1 to more than 36,250 by year-end, with over 10,000 prescribing healthcare providers.

CEO Bill Sibold framed the opportunity bluntly: “We solidified our position as the undisputed leader in MASH highlighted by nearly $1 billion in Rezdiffra sales in its first full year of launch. And we’re just getting started.” Roughly 90% of the target MASH population remains untreated, and the company has extended U.S. patent protection to 2045. The pipeline spans more than 10 programs, with MGL-2086 entering the clinic in Q2 2026 and MAESTRO-NASH OUTCOMES topline data due in 2027.

The catch: Madrigal remains unprofitable, with full-year operating income of -$300.10 million and a forward P/E of 667x. Analysts see upside anyway, with a target of $672.79 against a recent $514.41.

3. ADMA Biologics (ADMA) ADMA Biologics (NASDAQ:ADMA) takes the top slot because it is the only profitable name on the list, backed by multi-year guidance. Q4 2025 revenue came in at $139.16 million, up 18% year over year, EPS of $0.20 met expectations, and adjusted EBITDA jumped 52% to $73.59 million. Gross margin expanded to 64% from 54% as yield-enhanced production fully integrated into commercial operations. Full-year 2025 revenue was $510.17 million, up 20%, with net income of $146.93 million.

ASCENIV is the engine, generating $362.53 million in 2025, up 51%, with management noting it remains early in its penetration curve. Guidance calls for 2026 revenue above $635 million, 2027 above $775 million, and 2029 above $1.1 billion with adjusted EBITDA of at least $700 million, implying roughly 20% revenue and 30% EBITDA CAGRs. Capital returns are real: a $200 million repurchase program including a $125 million accelerated agreement with JPMorgan. CEO Adam Grossman said ADMA is “entering 2026 with significant momentum”.

Valuation is the most reasonable in the group: a trailing P/E of 18x and a forward P/E of 11x. Shares have been down 41.16% year to date, but rallied 14.47% over the past month since the Q4 print. Analysts carry a target of $20.67.

The Bottom Line Cytokinetics offers the most catalyst-rich 2026 calendar but the weakest balance sheet. Madrigal owns the MASH category outright with a launch that annualized above $1 billion within six quarters. ADMA earns the top spot by combining growth with actual earnings, margin expansion, capital returns, and the only multi-year revenue and EBITDA targets in the group. For investors looking past the AI trade, that combination is what respectable growth actually looks like.
2026-06-12 15:51 2mo ago
2026-05-05 08:00 4mo ago
Arrowhead Pharmaceuticals Licenses Clinical MASH Program Targeting PNPLA3 to Madrigal Pharmaceuticals
MDGL Madrigal Pharmaceuticals
FMP Stock News
Original source text
PASADENA, Calif.--(BUSINESS WIRE)---- $arwr--Arrowhead Pharmaceuticals, Inc. (NASDAQ: ARWR) today announced an exclusive worldwide license agreement with Madrigal Pharmaceuticals (NASDAQ: MDGL) for ARO-PNPLA3, Arrowhead's clinical stage RNA interference (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). “The early clinical data for ARO-PNPLA3 h.
2026-06-12 15:51 2mo ago
2026-05-05 08:00 4mo ago
Madrigal Adds Clinical-Stage siRNA Asset Targeting PNPLA3 to its MASH Pipeline
MDGL Madrigal Pharmaceuticals
FMP Stock News
Original source text
Company advances its leadership in MASH with clinical-stage, genetically targeted siRNA asset from Arrowhead PharmaceuticalsPrecision approach targets patients who have a mutation in the PNPLA3 gene, which is highly prevalent among Hispanic patients with MASHPhase 1 data published in The New England Journal of Medicine demonstrated a 46% liver fat reduction in homozygous patients and a well-tolerated safety profileMadrigal’s pipeline includes more than 10 programs at multiple stages of development, anchored by Rezdiffra® (resmetirom) as the foundational treatment CONSHOHOCKEN, Pa., May 05, 2026 (GLOBE NEWSWIRE) -- Madrigal Pharmaceuticals, Inc. (NASDAQ: MDGL), a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), today announced an exclusive global license agreement with Arrowhead Pharmaceuticals for ARO-PNPLA3, a clinical-stage, small interfering RNA (siRNA) asset targeting patatin-like phospholipase domain-containing protein 3 (PNPLA3), a key genetic driver of MASH.

The license of ARO-PNPLA3 adds to Madrigal’s pipeline with a precision medicine approach for patients at high risk of MASH. PNPLA3 I148M, a well-established genetic contributor to MASH progression, is associated with increased liver fat, inflammation, fibrosis, cirrhosis and hepatocellular carcinoma. Approximately 30% of patients with MASH with moderate to advanced fibrosis (consistent with stages F2 to F3 fibrosis) carry two identical copies of this variant (known as homozygous patients), and it is highly prevalent in Hispanic populations.

“The addition of an siRNA program targeting PNPLA3 to our pipeline reflects Madrigal’s commitment to shaping the future of MASH patient care,” said Bill Sibold, Chief Executive Officer of Madrigal. “MASH is a complex, heterogeneous disease, and we believe patients will benefit from personalized treatment strategies targeting key genetic risk factors that drive disease progression and adverse outcomes. We’re particularly excited about the potential to advance research for members of the Hispanic community, who are disproportionately affected by MASH.”

“We are pleased to add ARO-PNPLA3 to our pipeline as we continue to expand Madrigal’s leadership in MASH,” said David Soergel, M.D., Chief Medical Officer of Madrigal. “This licensing agreement advances our R&D strategy of developing therapies that target validated disease mechanisms and may complement Rezdiffra’s broad therapeutic effects, especially in patient populations with specific needs. Encouraging Phase 1 data support continued development of this targeted approach for patients with a well-defined genetic driver of disease, and we will begin planning for combination studies with Rezdiffra.”

Phase 1 trials provide proof-of-concept for ARO-PNPLA3 as a potential precision-medicine approach in MASH
A Phase 1, first-in-human, double-blind, placebo-controlled trial of ARO-PNPLA3 was conducted in the United States in 55 patients with Metabolic dysfunction-associated fatty liver disease (MAFLD) who were either homozygous or heterozygous carriers of the PNPLA3 I148M variant. Approximately 93% of participants were Hispanic or Latino. Data from this study, published in The New England Journal of Medicine, demonstrated:

Reductions in liver fat up to 46% (as measured by MRI-PDFF) at 12 weeks following a single dose at the highest dose level tested in PNPLA3 I148M homozygous patientsRapid onset of effect, with reductions observed at six weeks and sustained through at least 24 weeksNo clinically meaningful adverse events were observedNo effect on liver fat content was observed in heterozygous participants at any of the doses studiedResults from a second Phase 1 trial conducted in Japan (n=9) support these findings
siRNA: Potential for an Effective, Genetically Targeted Treatment Approach
Small interfering RNAs (siRNAs) offer a precision approach to gene silencing in MASH by selectively reducing the production of disease-driving proteins. When linked to a GalNAc ligand, siRNA molecules are delivered directly into hepatocytes, where they silence genes that have been identified as key risk factors for MASH by breaking down targeted mRNA. By pairing this precise gene-silencing approach with Rezdiffra, the company aims to explore whether reducing drivers of disease at the genetic level can complement Rezdiffra’s therapeutic effects. Madrigal currently has seven siRNA programs in its pipeline.

ARO-PNPLA3 is a GalNAc-conjugated siRNA designed to reduce expression of PNPLA3, a genetically validated driver of MASH. Mutations in the PNPLA3 gene have been shown to disrupt the liver’s ability to properly process fat. This leads to increased fat accumulation in hepatocytes, and is strongly associated with MASH progression and a high risk of developing hepatocellular carcinoma (HCC). The results of two Phase 1 trials suggested that a single dose of ARO-PNPLA3 reduced liver fat content in homozygous carriers of the PNPLA3 I148M variant, providing proof-of-concept for ARO-PNPLA3 as a precision-medicine approach in this patient population. Madrigal will consult with the FDA on design of a Phase 2 combination trial with Rezdiffra.

Deal Terms
Arrowhead has granted Madrigal an exclusive global license to develop, manufacture and commercialize ARO-PNPLA3. Arrowhead will receive an upfront payment of $25 million, additional payments of up to $975M if certain milestones are achieved and royalties on net sales.

About MASH
Metabolic dysfunction-associated steatohepatitis (MASH is a serious liver disease that can progress to cirrhosis, liver failure, liver cancer, the need for liver transplantation and premature mortality. MASH is the leading cause of liver transplantation in women and the second leading cause of all liver transplantation in the U.S., and the fastest-growing indication for liver transplantation in Europe.

Once patients progress to MASH with moderate to advanced liver fibrosis (consistent with stages F2 to F3 fibrosis), the risk of adverse liver outcomes increases dramatically: these patients have a 10 to 17 times higher risk of liver-related mortality as compared to patients without fibrosis.

Patients with MASH who progress to cirrhosis face a 42 times higher risk of liver-related mortality, underscoring the need to treat MASH before complications of cirrhosis develop. MASH is also an independent driver of cardiovascular disease, the leading cause of mortality for patients.

As disease awareness improves and disease prevalence increases, the number of diagnosed patients F2 to F4c MASH is growing.

About Rezdiffra 
What is Rezdiffra? 
Rezdiffra is a prescribed medicine used along with diet and exercise to treat adults with metabolic dysfunction-associated steatohepatitis (MASH) with moderate to advanced liver scarring (fibrosis), but not with cirrhosis of the liver.

This indication is approved based on improvement of MASH and liver scarring (fibrosis). There are ongoing studies to confirm the clinical benefit of Rezdiffra.

Before you take Rezdiffra, tell your healthcare provider about all of your medical conditions, including if you: 

have any liver problems other than MASH. have gallbladder problems or have been told you have gallbladder problems, including gallstones. are pregnant or plan to become pregnant. It is not known if Rezdiffra will harm your unborn baby.  A pregnancy safety study for women who take Rezdiffra during pregnancy collects information about the health of you and your baby. You or your healthcare provider can report your pregnancy by visiting https://pregnancyregistry.madrigalpharma.com/ or calling 1-800-905-0324. are breastfeeding or plan to breastfeed. It is not known if Rezdiffra passes into your breast milk. Talk to your healthcare provider about the best way to feed your baby if you take Rezdiffra. 
Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins and herbal supplements. 

Rezdiffra and other medicines may affect each other, causing side effects. Rezdiffra may affect the way other medicines work, and other medicines may affect how Rezdiffra works. Especially tell your healthcare provider if you take medicines that contain gemfibrozil to help lower your triglycerides, because Rezdiffra is not recommended in patients taking these medicines. Tell your healthcare provider if you are taking medicines such as clopidogrel to thin your blood or statin medicines to help lower your cholesterol. Know the medicines you take. Keep a list of them to show your healthcare provider and pharmacist when you get a new medicine.  What are the possible side effects of Rezdiffra? 
Rezdiffra may cause serious side effects, including: 

liver injury (hepatotoxicity). Stop taking Rezdiffra and call your healthcare provider right away if you develop the following signs or symptoms of hepatotoxicity: tiredness, nausea, vomiting, fever, rash, your skin or the white part of your eyes turns yellow (jaundice) or stomach pain/tenderness. gallbladder problems. Gallbladder problems such as gallstones, or inflammation of the gallbladder, or inflammation of the pancreas from gallstones can occur with MASH and may occur if you take Rezdiffra. Call your healthcare provider right away if you develop any signs or symptoms of these conditions including nausea, vomiting, fever, or pain in your stomach area (abdomen) that is severe and will not go away. The pain may be felt going from your abdomen to your back and the pain may happen with or without vomiting. The most common side effects of Rezdiffra include: diarrhea, nausea, itching, stomach pain, vomiting, dizziness and constipation. 
These are not all the possible side effects of Rezdiffra. For more information, ask your healthcare provider or pharmacist.

 Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088 or

www.fda.gov/medwatch. You may also report side effects to Madrigal at 1-800-905-0324.

 Please see the full

Prescribing Information, including

Patient Information, for Rezdiffra. 

About Madrigal
Madrigal Pharmaceuticals, Inc. (Nasdaq: MDGL) is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a liver disease with high unmet medical need. Madrigal’s medication, Rezdiffra (resmetirom), is a once-daily, oral, liver-directed THR-β agonist designed to target key underlying causes of MASH. Rezdiffra was the first medication approved by both the FDA and European Commission for the treatment of MASH with moderate to advanced fibrosis (F2 to F3). An ongoing Phase 3 outcomes trial is evaluating Rezdiffra for the treatment of compensated MASH cirrhosis (F4c). For more information, visit www.madrigalpharma.com and follow us on LinkedIn.

Forward-Looking Statements
This press release includes “forward-looking statements” made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995, as amended, including statements related to Madrigal’s development goals and timelines for its pipeline candidates, the potential benefit of ARO-PNPLA3 in the treatment of MASH and Madrigal’s ability to advance its leadership position in MASH treatment. Forward-looking statements are subject to a number of risks and uncertainties including, but not limited to: the assumptions underlying the forward-looking statements; Madrigal’s ability to successfully commercialize Rezdiffra; risks of obtaining and maintaining regulatory approvals, including, but not limited to, potential regulatory delays or rejections; the challenges with the commercial launch of a new product; Madrigal’s history of operating losses and the possibility that it may never achieve or maintain profitability; risks associated with meeting the objectives of Madrigal’s clinical trials, including, but not limited to Madrigal’s ability to achieve enrollment objectives concerning patient numbers (including an adequate safety database), outcomes objectives and/or timing objectives for Madrigal’s trials; any delays or failures in enrollment, and the occurrence of adverse safety events; risks related to the effects of Rezdiffra’s (resmetirom’s) or any product candidate’s mechanism of action; market demand for and acceptance of Rezdiffra; Madrigal’s ability to service indebtedness and otherwise comply with debt covenants; outcomes or trends from competitive trials; future topline data timing or results; Madrigal’s ability to prevent and/or mitigate cyber-attacks; the uncertainties inherent in clinical testing; uncertainties concerning analyses or assessments outside of a controlled clinical trial; Madrigal’s ability to protect its intellectual property; and changes in laws and regulations applicable to Madrigal’s business and its ability to comply with such laws and regulations. Undue reliance should not be placed on forward-looking statements, which speak only as of the date they are made. Madrigal undertakes no obligation to update any forward-looking statements to reflect new information, events, or circumstances after the date they are made, or to reflect the occurrence of unanticipated events. Please refer to Madrigal’s submissions filed with the U.S. Securities and Exchange Commission (“SEC”), for more detailed information regarding these risks and uncertainties and other factors that may cause actual results to differ materially from those expressed or implied. Madrigal specifically discusses these risks and uncertainties in greater detail in the sections appearing in Part I, Item 1A of its Annual Report on Form 10-K for the year ended December 31, 2025, filed with the SEC on February 19, 2026, and as updated from time to time by Madrigal’s other filings with the SEC.

Madrigal may use its website to comply with its disclosure obligations under Regulation FD. Therefore, investors should monitor Madrigal’s website in addition to following its press releases, filings with the SEC, public conference calls, and webcasts.

Investor Contact
Tina Ventura, [email protected]

Media Contact
Christopher Frates, [email protected]
2026-06-12 15:51 2mo ago
2026-05-06 07:00 4mo ago
Madrigal Pharmaceuticals Reports First-Quarter 2026 Financial Results and Provides Corporate Updates
MDGL Madrigal Pharmaceuticals
FMP Stock News
Original source text
CONSHOHOCKEN, Pa., May 06, 2026 (GLOBE NEWSWIRE) -- Madrigal Pharmaceuticals, Inc. (Nasdaq: MDGL), a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), today reports first-quarter 2026 financial results and provides corporate updates.
2026-06-12 15:51 2mo ago
2026-05-06 09:25 4mo ago
Madrigal (MDGL) Reports Q1 Loss, Beats Revenue Estimates
MDGL Madrigal Pharmaceuticals
FMP Stock News
Original source text
Madrigal (MDGL - Free Report) came out with a quarterly loss of $3.25 per share versus the Zacks Consensus Estimate of a loss of $3.61. This compares to a loss of $3.32 per share a year ago. These figures are adjusted for non-recurring items.

This quarterly report represents an earnings surprise of +9.97%. A quarter ago, it was expected that this biopharmaceutical company would post earnings of $0.04 per share when it actually produced a loss of $2.57, delivering a surprise of -6525%.

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

Madrigal, which belongs to the Zacks Medical - Drugs industry, posted revenues of $311.34 million for the quarter ended March 2026, surpassing the Zacks Consensus Estimate by 3.38%. This compares to year-ago revenues of $137.25 million. The company has topped consensus revenue estimates four 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.

Madrigal shares have lost about 13.7% since the beginning of the year versus the S&P 500's gain of 6%.

What's Next for Madrigal?While Madrigal 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 Madrigal was mixed. 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 #3 (Hold) for the stock. So, the shares are expected to perform in line with 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 -$1.21 on $343.76 million in revenues for the coming quarter and -$5.49 on $1.47 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, Medical - Drugs 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.

Stevanato Group (STVN - 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 7.

This maker of glass vials for COVID-19 vaccines is expected to post quarterly earnings of $0.12 per share in its upcoming report, which represents a year-over-year change of +9.1%. The consensus EPS estimate for the quarter has remained unchanged over the last 30 days.

Stevanato Group's revenues are expected to be $312.91 million, up 15.9% from the year-ago quarter.
2026-06-12 15:51 2mo ago
2026-05-06 14:01 4mo ago
Madrigal Pharmaceuticals, Inc. (MDGL) Q1 2026 Earnings Call Transcript
MDGL Madrigal Pharmaceuticals
FMP Stock News
Original source text
Madrigal Pharmaceuticals, Inc. (MDGL) Q1 2026 Earnings Call Transcript
2026-06-12 15:51 2mo ago
2026-05-07 12:35 4mo ago
Madrigal Q1 Earnings Beat, MASH Drug Sales Drive Top Line, Stock Up
MDGL Madrigal Pharmaceuticals
FMP Stock News
Original source text
Key Takeaways MDGL posted Q1 revenues of $311.3M, fueled entirely by strong Rezdiffra sales growth in MASH.Rezdiffra reached 42,250 treated patients by March-end, up 2.5 times from Q1 2025 levels.Madrigal is advancing multiple late-stage Rezdiffra studies, with key data expected in 2027 and 2028. Madrigal Pharmaceuticals (MDGL - Free Report) reported first-quarter 2026 loss of $3.25 per share, narrower than the Zacks Consensus Estimate of a loss of $3.61. In the same quarter last year, the company had incurred a loss of $2.61 per share.

In the first quarter, MDGL generated total revenues of $311.3 million, up significantly year over year, entirely from product sales of its metabolic dysfunction-associated steatohepatitis (MASH) drug Rezdiffra (resmetirom), which was approved in 2024. The metric beat the Zacks Consensus Estimate of $301 million. Rezdiffra is the first marketed drug in MDGL’s portfolio, which was launched in April 2024 and posted significant year-over-year growth, driven by increased demand.

Madrigal shares gained 7.4% on Wednesday, as investors were impressed by the better-than-expected earnings results.

MDGL’s Q4 Results in DetailIn March 2024, the FDA granted accelerated approval to Rezdiffra, making it the first and currently the only approved therapy for the MASH indication. The eligible patient population includes adults with noncirrhotic MASH with moderate to advanced liver fibrosis. Rezdiffra has also received conditional approval as the first and only therapy in the EU to treat adults with noncirrhotic MASH with moderate-to-advanced liver fibrosis. Per Madrigal, more than 42,250patients are receiving the treatment as of March 31, 2026, up 2.5 times from first-quarter 2025, reflecting continued strong physician adoption and high patient demand.

During the quarter, research and development expenses more than doubled to $108.7 million in the first quarter of 2026. The massive increase can be primarily attributed to one-time, upfront business development expenses of $54.3 million.

Year to date, Madrigal shares have lost 7.3% against the industry’s 0.9% growth.

Image Source: Zacks Investment Research

Selling, general and administrative expenses also nearly doubled in the reported quarter to $268.5 million. This exponential rise was on account of increased commercial launch activities for Rezdiffra, including significant increases in headcount to support marketing efforts.

Madrigal had cash, cash equivalents and marketable securities worth $817.9 million as of March 31, 2026, compared with $988.6 million as of Dec. 31, 2025.

MDGL’s Pipeline & Other UpdatesAs the FDA and EU approved Rezdiffra under the accelerated pathway, the continued approval will be based on promising long-term safety and efficacy data from the pivotal phase III MAESTRO-NASH biopsy study. This late-stage study, which provided the data for the drug's accelerated approval for MASH, is ongoing as an outcomes study, with data expected in 2028. The goal is to generate confirmatory 54-month data to verify the drug's clinical benefits and support full approval for the noncirrhotic MASH indication.

In addition to the study, a second phase III outcomes study (MAESTRO-NASH OUTCOMES) is underway, evaluating the progression to liver decompensation events in patients with compensated MASH cirrhosis treated with Rezdiffra compared with placebo. Top-line data is expected in 2027. A positive outcome from this study is also expected to support the full approval of Rezdiffra for noncirrhotic MASH and expand the eligible patient population for Rezdiffra with an additional indication.

The open-label extension (OLE) arm of the MAESTRO-NAFLD-1 study is also currently evaluating the drug in patients with compensated MASH cirrhosis. In 2025, Madrigal reported positive two-year data from the OLE arm. The results reinforce Rezdiffra’s potential benefit for patients with compensated MASH cirrhosis and support the ongoing MAESTRO-NASH OUTCOMES study's potential success.

Earlier in 2026, Madrigal also added six preclinical siRNA programs to strengthen its pipeline and advance next-generation, genetically targeted MASH therapies alongside Rezdiffra. Such efforts demonstrate MDGL’s commitment to establishing the drug as the standard-of-care treatment for MASH.

Recently, Madrigal expanded its MASH pipeline through a licensing agreement with Arrowhead Pharmaceuticals for global rights to ARO-PNPLA3, a clinical-stage siRNA candidate targeting the genetically validated PNPLA3 mutation linked to MASH. The asset is aimed at a genetically defined patient population representing roughly 30% of moderate-to-advanced fibrosis cases, with phase I data showing up to a 46% reduction in liver fat after a single high dose in PNPLA3 homozygous patients.

MDGL’s Zacks Rank & Stocks to ConsiderMadrigal currently carries a Zacks Rank #3 (Hold).

Some better-ranked stocks in the biotech sector are Catalyst Pharmaceuticals (CPRX - Free Report) , Immatics (IMTX - Free Report) and Inovio Pharmaceuticals (INO - Free Report) , each carrying a Zacks Rank #2 (Buy) at present. You can see the complete list of today’s Zacks #1 Rank (Strong Buy) stocks here.

Over the past 60 days, estimates for Catalyst Pharmaceuticals’ 2026 EPS have declined from $2.82 to $2.79. CPRX shares have gained 30.8% year to date.

Catalyst Pharmaceuticals’ earnings beat estimates in each of the trailing four quarters, with the average surprise being 35.19%.

Over the past 60 days, estimates for Immatics’ 2026 loss per share have narrowed from $1.61 to $1.49. IMTX shares have gained 9.6% year to date.

Immatics’ earnings beat estimates in three of the trailing four quarters and missed on the remaining occasion, delivering an average negative surprise of 8.06%.

Over the past 60 days, estimates for Inovio Pharmaceuticals’ 2026 loss per share have narrowed from $1.26 to $1.06. INO shares have plunged 28.8% year to date.

Inovio Pharmaceuticals’ earnings beat estimates in each of the trailing four quarters, with the average surprise being 57.94%.
2026-06-12 15:51 2mo ago
2026-05-07 16:05 4mo ago
Madrigal Pharmaceuticals Announces Grants of Inducement Awards under Nasdaq Listing Rule 5635(c)(4)
MDGL Madrigal Pharmaceuticals
FMP Stock News
Original source text
May 07, 2026 16:05 ET  | Source: Madrigal Pharmaceuticals, Inc.

CONSHOHOCKEN, Pa., May 07, 2026 (GLOBE NEWSWIRE) -- Madrigal Pharmaceuticals, Inc. (NASDAQ:MDGL), a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), today announced that it granted equity awards on May 1, 2026 to 47 new non-executive employees as equity inducement awards under the terms of Madrigal’s 2025 Inducement Plan. The equity awards were approved by Madrigal’s independent Compensation Committee in accordance with Nasdaq Listing Rule 5635(c)(4).

The equity awards were granted as an inducement material to employees’ acceptance of employment with the company. The new employees received, in the aggregate, options to purchase 5,312 shares of Madrigal’s common stock, 17,589 time-based restricted stock units and 1,839 performance-based restricted stock units. Options have an exercise price of $513.72 per share, which is equal to the closing price of the company’s common stock on the grant date. Options vest as follows: (i) 25% of the option shares will vest on the first anniversary of the grant date and (ii) 6.25% of the option shares will vest on each quarterly anniversary following the first anniversary of the grant date. All restricted stock units granted vest in four equal installments on each of the first through fourth anniversaries of the grant date. Performance-based restricted stock units are earned based on the total shareholder return of Madrigal relative to a defined peer group over a three year period and, to the extent earned, will cliff vest in the first quarter of 2029. The vesting of all awards described above shall be subject to each such employee’s continued employment as of the applicable vesting date.

About Madrigal Pharmaceuticals

Madrigal Pharmaceuticals, Inc. (Nasdaq: MDGL) is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a liver disease with high unmet medical need. Madrigal’s medication, Rezdiffra (resmetirom), is a once-daily, oral, liver-directed THR-β agonist designed to target key underlying causes of MASH. Rezdiffra was the first medication approved by both the FDA and European Commission for the treatment of MASH with moderate to advanced fibrosis (F2 to F3). An ongoing Phase 3 outcomes trial is evaluating Rezdiffra for the treatment of compensated MASH cirrhosis (F4c). For more information, visit www.madrigalpharma.com.

Investor Contact
Tina Ventura, [email protected]

Media Contact
Christopher Frates, [email protected]
2026-06-12 15:51 2mo ago
2026-05-20 08:00 3mo ago
Madrigal to Present New Data from the Company's MASH Program at EASL 2026 Demonstrating the Effects of Rezdiffra on Markers of Cardiovascular and Portal Hypertension Risk
MDGL Madrigal Pharmaceuticals
FMP Stock News
Original source text
Secondary analysis from the Phase 3 MAESTRO-NASH and MAESTRO-NAFLD-1 trials examines improvements in lipid profiles for Lp(a), LDL-C and ApoB with Rezdiffra® (resmetirom)Analysis of two-year data in patients with compensated MASH cirrhosis (F4c) examines improvement in ANTICIPATE-NASH risk scores, a marker for clinically significant portal hypertensionAdditional abstracts focus on early real-world evidence with Rezdiffra and the ability of noninvasive biomarkers to predict fibrosis improvement in patients treated with Rezdiffra CONSHOHOCKEN, Pa., May 20, 2026 (GLOBE NEWSWIRE) -- Madrigal Pharmaceuticals, Inc. (NASDAQ: MDGL), a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), today announced that multiple abstracts from its Rezdiffra development and real-world evidence programs will be presented at the European Association for the Study of the Liver (EASL) Congress 2026, taking place May 27–30 in Barcelona, Spain.

The presentations highlight the breadth of evidence supporting Rezdiffra, including a secondary analysis on cardiometabolic risk in patients with MASH, non-invasive risk stratification in patients with compensated cirrhosis and early real-world evidence from routine clinical practice.

“The body of data presented at EASL 2026 reinforces Madrigal’s leadership in MASH and clearly supports the continued integration of Rezdiffra into clinical practice as a foundational therapy,” said David Soergel, M.D., Chief Medical Officer of Madrigal. “These analyses extend beyond liver-focused assessments to explore Rezdiffra’s effects on markers of cardiovascular risk and provide important new insights about noninvasive measures of treatment response in patients with moderate to advanced fibrosis (F2-F3) and well-compensated MASH cirrhosis (F4c).”

Madrigal Poster Presentations at the EASL Congress 2026:

TitlePresenterReducing CV risk in patients with MASH independent of baseline based on Lp(a) and LDL lowering by resmetiromMeena BansalBaseline ANTICIPATE score and response predicts liver outcome events in a 180 patient MASH cirrhosis cohort treated with resmetiromNaim AlkhouriIn F0-F1 and F2-F3 MASH, ≥5% weight loss significantly lowers VCTE and ELF independent of biopsy fibrosis improvement; resmetirom and not placebo reduction of ELF and VCTE are associated with biopsy improvement of fibrosis, independent of weight lossRohit LoombaEarly real-world effectiveness of resmetirom in adults with metabolic dysfunction associated steatohepatitis and moderate-to-advanced fibrosisNaim AlkhouriTwelve-month changes in liver function enzymes and lipids in patients receiving resmetiromChristina ParrinelloNon-invasive test-driven modeling of patient eligibility for resmetirom therapy in MASLD: Data from the German SLD-RegistryMaurice MichelEarly and Week 52 biomarker (MRI-PDFF, ALT, MRE and PRO-C3) responses to resmetirom predict improvements in MASH and liver fibrosisRohit LoombaMachine learning models of non-invasive tests to predict MASH and fibrosis stage based on MAESTRO-NAFLD-1 and MAESTRO-NASH liver biopsiesRohit Loomba Rezdiffra (resmetirom) is a once-daily, oral, liver-directed thyroid hormone receptor (THR)-β agonist designed to address key underlying causes of MASH. It was the first medication approved for the treatment of MASH in the U.S. and Europe. In the pivotal Phase 3 MAESTRO-NASH biopsy trial, Rezdiffra achieved both fibrosis improvement and MASH resolution primary endpoints. Rezdiffra also reduced liver stiffness, liver fat, liver enzymes and atherogenic lipids in the MAESTRO-NASH trial and improved health-related quality of life. At one year, 91% of patients treated with Rezdiffra 100mg achieved improvement or stabilization of liver stiffness as measured by vibrational-controlled transient elastography (VCTE), a test that is frequently used to monitor treatment response in clinical practice.

Rezdiffra is indicated in conjunction with diet and exercise for the treatment of adults with noncirrhotic MASH with moderate to advanced liver fibrosis (consistent with stages F2 to F3 fibrosis). Continued approval for this indication may be contingent upon verification and description of clinical benefit in ongoing confirmatory trials. Rezdiffra is not approved in any geography for the treatment of patients with cirrhosis.

About MASH
Metabolic dysfunction-associated steatohepatitis (MASH) is a serious liver disease that can progress to cirrhosis, liver failure, liver cancer, the need for liver transplantation and premature mortality. MASH is the leading cause of liver transplantation in women and the second leading cause of all liver transplantation in the U.S., and the fastest-growing indication for liver transplantation in Europe.

Once patients progress to MASH with moderate to advanced liver fibrosis (consistent with stages F2 to F3 fibrosis), the risk of adverse liver outcomes increases dramatically: these patients have a 10 to 17 times higher risk of liver-related mortality as compared to patients without fibrosis.

Patients with MASH who progress to cirrhosis face a 42 times higher risk of liver-related mortality, underscoring the need to treat MASH before complications of cirrhosis develop. MASH is also an independent driver of cardiovascular disease, the leading cause of mortality for patients.

As disease awareness improves and disease prevalence increases, the number of diagnosed patients F2 to F4c MASH is growing.

About Rezdiffra
What is Rezdiffra?
Rezdiffra is a prescribed medicine used along with diet and exercise to treat adults with metabolic dysfunction-associated steatohepatitis (MASH) with moderate to advanced liver scarring (fibrosis), but not with cirrhosis of the liver.

This indication is approved based on improvement of MASH and liver scarring (fibrosis). There are ongoing studies to confirm the clinical benefit of Rezdiffra.

Before you take Rezdiffra, tell your healthcare provider about all of your medical conditions, including if you:

have any liver problems other than MASH.have gallbladder problems or have been told you have gallbladder problems, including gallstones.are pregnant or plan to become pregnant. It is not known if Rezdiffra will harm your unborn baby. A pregnancy safety study for women who take Rezdiffra during pregnancy collects information about the health of you and your baby. You or your healthcare provider can report your pregnancy by visiting https://pregnancyregistry.madrigalpharma.com/ or calling 1-800-905-0324. are breastfeeding or plan to breastfeed. It is not known if Rezdiffra passes into your breast milk. Talk to your healthcare provider about the best way to feed your baby if you take Rezdiffra.
Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins and herbal supplements.

Rezdiffra and other medicines may affect each other, causing side effects. Rezdiffra may affect the way other medicines work, and other medicines may affect how Rezdiffra works.Especially tell your healthcare provider if you take medicines that contain gemfibrozil to help lower your triglycerides, because Rezdiffra is not recommended in patients taking these medicines.Tell your healthcare provider if you are taking medicines such as clopidogrel to thin your blood or statin medicines to help lower your cholesterol.Know the medicines you take. Keep a list of them to show your healthcare provider and pharmacist when you get a new medicine. What are the possible side effects of Rezdiffra?
Rezdiffra may cause serious side effects, including:

liver injury (hepatotoxicity). Stop taking Rezdiffra and call your healthcare provider right away if you develop the following signs or symptoms of hepatotoxicity: tiredness, nausea, vomiting, fever, rash, your skin or the white part of your eyes turns yellow (jaundice) or stomach pain/tenderness.gallbladder problems. Gallbladder problems such as gallstones, or inflammation of the gallbladder, or inflammation of the pancreas from gallstones can occur with MASH and may occur if you take Rezdiffra. Call your healthcare provider right away if you develop any signs or symptoms of these conditions including nausea, vomiting, fever, or pain in your stomach area (abdomen) that is severe and will not go away. The pain may be felt going from your abdomen to your back and the pain may happen with or without vomiting.The most common side effects of Rezdiffra include: diarrhea, nausea, itching, stomach pain, vomiting, dizziness and constipation.
These are not all the possible side effects of Rezdiffra. For more information, ask your healthcare provider or pharmacist.

Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. You may also report side effects to Madrigal at 1-800-905-0324.

Please see the full Prescribing Information, including Patient Information, for Rezdiffra.

About Madrigal
Madrigal Pharmaceuticals, Inc. (Nasdaq: MDGL) is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a liver disease with high unmet medical need. Madrigal’s medication, Rezdiffra (resmetirom), is a once-daily, oral, liver-directed THR-β agonist designed to target key underlying causes of MASH. Rezdiffra was the first medication approved by both the FDA and European Commission for the treatment of MASH with moderate to advanced fibrosis (F2 to F3). An ongoing Phase 3 outcomes trial is evaluating Rezdiffra for the treatment of compensated MASH cirrhosis (F4c). For more information, visit www.madrigalpharma.com and follow us on LinkedIn.

Forward-Looking Statements
This press release includes “forward-looking statements” made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995, as amended, including statements related to Rezdiffra’s effects on markers of cardiovascular risk and the potential benefit of Rezdiffra in patients with compensated MASH cirrhosis. Forward-looking statements are subject to a number of risks and uncertainties including, but not limited to: the assumptions underlying the forward-looking statements; our ability to successfully commercialize Rezdiffra in the U.S. and Europe; risks related to obtaining and maintaining regulatory approvals, including, but not limited to, potential regulatory delays or rejections; our history of operating losses and the possibility that we may never achieve or maintain profitability; risks associated with meeting the objectives of our clinical trials, including, but not limited to our ability to achieve enrollment objectives concerning patient numbers (including an adequate safety database), outcomes objectives and/or timing objectives for our trials; any delays or failures in enrollment, and the occurrence of adverse safety events; risks related to the effects of Rezdiffra’s (resmetirom’s) mechanism of action or of any other product candidate; market demand for and acceptance of Rezdiffra; our ability to service indebtedness and otherwise comply with debt covenants; outcomes or trends from competitors; future topline data timing or results; our ability to prevent and/or mitigate cyber-attacks; our ability to protect our intellectual property rights; the uncertainties inherent in clinical testing; uncertainties concerning analyses or assessments outside of a controlled clinical trial; and changes in laws and regulations applicable to our business and our ability to comply with such laws and regulations. Undue reliance should not be placed on forward-looking statements, which speak only as of the date they are made. Madrigal undertakes no obligation to update any forward-looking statements to reflect new information, events, or circumstances after the date they are made, or to reflect the occurrence of unanticipated events. Please refer to Madrigal’s submissions filed with the U.S. Securities and Exchange Commission (SEC) for more detailed information regarding these risks and uncertainties and other factors that may cause actual results to differ materially from those expressed or implied. Madrigal specifically discusses these risks and uncertainties in greater detail in the sections appearing in Part 1A of its Annual Report on Form 10-K for the year ended December 31, 2025, and as updated from time to time by Madrigal’s other filings with the SEC.

Madrigal may use its website to comply with its disclosure obligations under Regulation FD. Therefore, investors should monitor Madrigal’s website in addition to following its press releases, filings with the SEC, public conference calls, and webcasts.

Madrigal Pharmaceuticals, Rezdiffra® and associated logos are trademarks of Madrigal Pharmaceuticals, Inc.

Investor Contact
Tina Ventura, [email protected]

Media Contact
Christopher Frates, [email protected]
2026-06-12 15:51 2mo ago
2026-05-21 16:05 3mo ago
Madrigal Pharmaceuticals Announces Grants of Inducement Awards under Nasdaq Listing Rule 5635(c)(4)
MDGL Madrigal Pharmaceuticals
FMP Stock News
Original source text
May 21, 2026 16:05 ET  | Source: Madrigal Pharmaceuticals, Inc.

CONSHOHOCKEN, Pa., May 21, 2026 (GLOBE NEWSWIRE) -- Madrigal Pharmaceuticals, Inc. (NASDAQ:MDGL), a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), today announced that it granted equity awards on May 15, 2026 to 15 new non-executive employees as equity inducement awards under the terms of Madrigal’s 2025 Inducement Plan. The equity awards were approved by Madrigal’s independent Compensation Committee in accordance with Nasdaq Listing Rule 5635(c)(4).

The equity awards were granted as an inducement material to employees’ acceptance of employment with the company. The new employees received, in the aggregate, 5,308 time-based restricted stock units. All restricted stock units granted vest in four equal installments on each of the first through fourth anniversaries of the grant date. The vesting of all awards described above shall be subject to each such employee’s continued employment as of the applicable vesting date.

About Madrigal Pharmaceuticals

Madrigal Pharmaceuticals, Inc. (Nasdaq: MDGL) is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a liver disease with high unmet medical need. Madrigal’s medication, Rezdiffra (resmetirom), is a once-daily, oral, liver-directed THR-β agonist designed to target key underlying causes of MASH. Rezdiffra was the first medication approved by both the FDA and European Commission for the treatment of MASH with moderate to advanced fibrosis (F2 to F3). An ongoing Phase 3 outcomes trial is evaluating Rezdiffra for the treatment of compensated MASH cirrhosis (F4c). For more information, visit www.madrigalpharma.com.

Investor Contact
Tina Ventura, [email protected]

Media Contact
Christopher Frates, [email protected]
2026-06-12 15:51 2mo ago
2026-05-27 08:00 3mo ago
Madrigal Presents Data Demonstrating Rezdiffra Reduced Markers of Cardiovascular and Liver-Related Risk in Patients with MASH
MDGL Madrigal Pharmaceuticals
FMP Stock News
Original source text
Growing body of clinical and real-world evidence supports the role of Rezdiffra® (resmetirom) as the foundational therapy for patients with MASH Rezdiffra improved atherogenic lipid profiles associated with cardiovascular risk, including LDL-C, ApoB and Lp(a), in a secondary analysis from the Phase 3 MAESTRO program In patients with well-compensated MASH cirrhosis (F4c), Rezdiffra improved a risk score – ANTICIPATE-NASH – that predicts the probability of experiencing severe liver-related eventsMultiple real-world analyses evaluating the use of Rezdiffra in routine clinical practice demonstrated early and sustained improvements in cardiometabolic parameters, liver-related biomarkers, and liver stiffness measurements; 49% of patients achieved ≥25% reduction in liver stiffness over a nine-month follow-up period CONSHOHOCKEN, Pa., May 27, 2026 (GLOBE NEWSWIRE) -- Madrigal Pharmaceuticals, Inc. (NASDAQ: MDGL), a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), today announced new analyses of Phase 3 data and real-world evidence demonstrating Rezdiffra reduced markers of cardiovascular and liver-related risk in patients with MASH. The data are featured across eight poster presentations at the European Association for the Study of the Liver (EASL) Congress 2026, taking place May 27-30 in Barcelona, Spain.

“New analyses from the Phase 3 MAESTRO program and a growing body of real-world evidence reinforce Rezdiffra’s position as the foundational therapy for MASH,” said David Soergel, M.D., Chief Medical Officer of Madrigal. “The data we are presenting at the EASL Congress give us new insight into Rezdiffra’s potential to reduce clinically significant portal hypertension risk in patients with well-compensated MASH cirrhosis, a population with no approved therapies. Additionally, we continue to generate evidence supporting the medication’s broad and consistent effects on key biomarkers used to monitor treatment response in everyday clinical practice, as well as markers of cardiovascular risk.”

“Cardiovascular disease is the leading cause of death in people with MASH, so the secondary analysis from the Phase 3 MAESTRO program demonstrating that Rezdiffra improved LDL-C, ApoB and Lp(a) is highly relevant for clinicians and patients,” said Meena B. Bansal, M.D., F.A.A.S.L.D., System Chief, Division of Liver Diseases Director, MASH/NASH Center of Excellence, Icahn School of Medicine at Mount Sinai. “Patients achieved key MASH endpoints and significant improvements in multiple atherogenic lipids and lipoproteins regardless of baseline statin use. This is particularly important because statins are not known to meaningfully lower certain lipoproteins such as Lp(a). These results suggest Rezdiffra may provide additional cardiometabolic benefit for patients with MASH, whether or not they are receiving statin therapy. Further research is warranted to evaluate Rezdiffra’s potential to improve cardiovascular outcomes in patients with MASH.”

Key Madrigal Data Presentations at the EASL Congress 2026

Poster Presentation: Reducing CV risk in patients with MASH independent of baseline statin use: Lp(a) and LDL lowering by resmetirom [Abstract # ID-FRI-149, Presenter: Meena B. Bansal]

Data from a secondary analysis of the Phase 3 MAESTRO-NASH and MAESTRO-NAFLD-1 trials demonstrated that Rezdiffra improved key histologic MASH endpoints and significantly reduced multiple atherogenic lipids and lipoproteins associated with cardiovascular risk, including LDL-C and Lp(a), regardless of baseline statin use.

Among statin-treated patients (n=473) receiving Rezdiffra 100mg:

44.4% of patients with baseline LDL-C ≥70mg/dL shifted to <70mg/dL at week 52.50.0% of patients with baseline LDL-C ≥100mg/dL shifted to <100mg/dL at week 52.Among patients with elevated baseline Lp(a), 36.3% of patients with baseline Lp(a) ≥30mg/dL and 37.5% of patients with baseline Lp(a) ≥50mg/dL shifted below those thresholds.No significant statin-related safety signals were observed. Among patients receiving Rezdiffra 100mg and no statins (n=493):

13.8% of patients with baseline LDL-C ≥70mg/dL shifted to <70mg/dL at week 52.51.5% of patients with baseline LDL-C ≥100mg/dL shifted to <100mg/dL at week 52.Among patients with elevated baseline Lp(a), 45.4% of patients with baseline Lp(a) ≥30mg/dL and 62.5% of patients with baseline Lp(a) ≥50mg/dL shifted below those thresholds. These findings support the concomitant use of Rezdiffra with statin therapy and suggest the potential for Rezdiffra to address both liver disease and cardiometabolic risk in patients with MASH.

EASL Top Poster: Baseline ANTICIPATE score and response predicts liver outcome events in a 180 patient MASH cirrhosis cohort treated with resmetirom [Abstract # ID-TOP-177, Presenter: Naim Alkhouri]

In patients with compensated MASH cirrhosis, clinically significant portal hypertension (CSPH) is a key driver of disease progression and severe liver-related complications. While Baveno criteria are used to identify patients likely to have CSPH, ANTICIPATE-NASH is a noninvasive risk stratification model developed for MASH that integrates liver stiffness measurements, platelet count and body mass index (BMI) to estimate future CSPH risk and predict the likelihood of liver-related events over the subsequent three years.

The ANTICIPATE-NASH risk model was applied to the open-label extension (OLE) cohort from the MAESTRO-NAFLD-1 trial, which included patients with well-compensated MASH cirrhosis (F4c) treated with Rezdiffra for up to two years. Results demonstrated progressive improvements in ANTICIPATE-NASH risk scores over time:

The proportion of patients classified as high risk for CSPH decreased from 75% at baseline to 60.3% at Year 1 and 54.5% at Year 2.Mean ANTICIPATE-NASH scores declined by up to 37.6% over two years of treatment.Liver-related events were infrequent and occurred exclusively in patients with baseline ANTICIPATE-NASH scores associated with elevated CSPH risk. These findings support the potential use of ANTICIPATE-NASH as a risk stratification tool to identify patients with a high-risk of disease progression, informing prognosis and clinical decision-making.

Additional Poster Presentations (Real-World Data):

Early real-world effectiveness of resmetirom in adults with metabolic dysfunction associated steatohepatitis and moderate-to-advanced- fibrosis [Abstract #ID-FRI-141, Presenter: Naim Alkhouri]Twelve-month changes in liver function enzymes and lipids in patients receiving resmetirom [Abstract # ID-FRI-186, Presenter: Anthony Martinez]Non-invasive test-driven modeling of patient eligibility for resmetirom therapy in MASLD: Data from the German SLD-Registry [Abstract #ID-WED-155, Presenter: Maurice Michel] Multiple real-world studies evaluating patients treated with Rezdiffra for up to 12 months in routine clinical practice are also being presented at EASL. Collectively, these studies demonstrated that patients achieved clinically meaningful improvements in biomarkers of liver disease and cardiometabolic risk. Improvements were observed as early as approximately six months following treatment initiation and sustained through approximately 12 months. Rezdiffra was generally well tolerated, with low rates of treatment-related adverse events and discontinuations reported in routine clinical practice.

Abstract #ID-FRI-141: In an analysis of data from a large gastroenterology practice, Rezdiffra use was associated with clinically meaningful improvements in laboratory and non-invasive clinical measures. Over a mean follow-up period of approximately nine months, 48.6% of patients achieved ≥25% reduction in liver stiffness, a key measure of treatment response. Rezdiffra was well tolerated in this analysis, and discontinuation due to treatment-related adverse events was <1%.Abstract # ID-FRI-186: In another electronic health record analysis of 728 patients treated with Rezdiffra over 12 months, statistically significant reductions in ALT and AST were observed; these reductions in liver enzymes were consistent across all subgroups, irrespective of baseline type 2 diabetes status, obesity, GLP-1 and statin use. LDL-C levels also decreased significantly in the overall cohort and showed directional reductions across all subgroups.Abstract #ID-WED-155: A prospective registry study (Germany Steatotic Liver Disease [SLD]) aimed to characterize patients eligible for Rezdiffra treatment based on noninvasive tests (NITs) in a real-world cohort in Germany. Of the 1,308 patients analyzed, approximately one in five met the criteria for treatment. The treatment-eligible cohort showed a higher distribution of three or more metabolic comorbidities simultaneously. Identification of such patients using NITs such as liver stiffness may support risk stratification and inform treatment strategies in routine clinical practice. About Rezdiffra
Rezdiffra (resmetirom) is a once-daily, oral, liver-directed thyroid hormone receptor (THR)-β agonist designed to address key underlying causes of MASH. It was the first medication approved for the treatment of MASH in the U.S. and Europe. In the pivotal Phase 3 MAESTRO-NASH biopsy trial, Rezdiffra achieved both fibrosis improvement and MASH resolution primary endpoints. Rezdiffra also reduced liver stiffness, liver fat, liver enzymes and atherogenic lipids in the MAESTRO-NASH trial and improved health-related quality of life. At one year, 91% of patients treated with Rezdiffra 100mg achieved improvement or stabilization of liver stiffness.

Rezdiffra is indicated in conjunction with diet and exercise for the treatment of adults with noncirrhotic MASH with moderate to advanced liver fibrosis (consistent with stages F2 to F3 fibrosis). Continued approval for this indication may be contingent upon verification and description of clinical benefit in ongoing confirmatory trials. Rezdiffra is not approved in any geography for the treatment of patients with cirrhosis.

About MASH
Metabolic dysfunction-associated steatohepatitis (MASH) is a serious liver disease that can progress to cirrhosis, liver failure, liver cancer, the need for liver transplantation and premature mortality. MASH is the leading cause of liver transplantation in women and the second leading cause of all liver transplantation in the U.S., and the fastest-growing indication for liver transplantation in Europe.

Once patients progress to MASH with moderate to advanced liver fibrosis (consistent with stages F2 to F3 fibrosis), the risk of adverse liver outcomes increases dramatically: these patients have a 10 to 17 times higher risk of liver-related mortality as compared to patients without fibrosis.

Patients with MASH who progress to cirrhosis face a 42 times higher risk of liver-related mortality, underscoring the need to treat MASH before complications of cirrhosis develop. MASH is also an independent driver of cardiovascular disease, the leading cause of mortality for patients.

As disease awareness improves and disease prevalence increases, the number of diagnosed patients with F2 to F4c MASH is growing.

What is Rezdiffra?
Rezdiffra is a prescribed medicine used along with diet and exercise to treat adults with metabolic dysfunction-associated steatohepatitis (MASH) with moderate to advanced liver scarring (fibrosis), but not with cirrhosis of the liver.

This indication is approved based on improvement of MASH and liver scarring (fibrosis). There are ongoing studies to confirm the clinical benefit of Rezdiffra.

Before you take Rezdiffra, tell your healthcare provider about all of your medical conditions, including if you:

have any liver problems other than MASH.have gallbladder problems or have been told you have gallbladder problems, including gallstones.are pregnant or plan to become pregnant. It is not known if Rezdiffra will harm your unborn baby. A pregnancy safety study for women who take Rezdiffra during pregnancy collects information about the health of you and your baby. You or your healthcare provider can report your pregnancy by visiting https://pregnancyregistry.madrigalpharma.com/ or calling 1-800-905-0324. are breastfeeding or plan to breastfeed. It is not known if Rezdiffra passes into your breast milk. Talk to your healthcare provider about the best way to feed your baby if you take Rezdiffra. Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins and herbal supplements.

Rezdiffra and other medicines may affect each other, causing side effects. Rezdiffra may affect the way other medicines work, and other medicines may affect how Rezdiffra works.Especially tell your healthcare provider if you take medicines that contain gemfibrozil to help lower your triglycerides, because Rezdiffra is not recommended in patients taking these medicines.Tell your healthcare provider if you are taking medicines such as clopidogrel to thin your blood or statin medicines to help lower your cholesterol.Know the medicines you take. Keep a list of them to show your healthcare provider and pharmacist when you get a new medicine. What are the possible side effects of Rezdiffra?
Rezdiffra may cause serious side effects, including:

liver injury (hepatotoxicity). Stop taking Rezdiffra and call your healthcare provider right away if you develop the following signs or symptoms of hepatotoxicity: tiredness, nausea, vomiting, fever, rash, your skin or the white part of your eyes turns yellow (jaundice) or stomach pain/tenderness.gallbladder problems. Gallbladder problems such as gallstones, or inflammation of the gallbladder, or inflammation of the pancreas from gallstones can occur with MASH and may occur if you take Rezdiffra. Call your healthcare provider right away if you develop any signs or symptoms of these conditions including nausea, vomiting, fever, or pain in your stomach area (abdomen) that is severe and will not go away. The pain may be felt going from your abdomen to your back and the pain may happen with or without vomiting.The most common side effects of Rezdiffra include: diarrhea, nausea, itching, stomach pain, vomiting, dizziness and constipation. These are not all the possible side effects of Rezdiffra. For more information, ask your healthcare provider or pharmacist.

Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. You may also report side effects to Madrigal at 1-800-905-0324.

Please see the full Prescribing Information, including Patient Information, for Rezdiffra.

About Madrigal
Madrigal Pharmaceuticals, Inc. (Nasdaq: MDGL) is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a liver disease with high unmet medical need. Madrigal’s medication, Rezdiffra (resmetirom), is a once-daily, oral, liver-directed THR-β agonist designed to target key underlying causes of MASH. Rezdiffra was the first medication approved by both the FDA and European Commission for the treatment of MASH with moderate to advanced fibrosis (F2 to F3). An ongoing Phase 3 outcomes trial is evaluating Rezdiffra for the treatment of compensated MASH cirrhosis (F4c). For more information, visit www.madrigalpharma.com and follow us on LinkedIn.

Forward-Looking Statements
This press release includes “forward-looking statements” made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995, as amended, including statements related to Rezdiffra’s ability to potentially improve cardiovascular outcomes in patients with MASH and the potential benefit of Rezdiffra in patients with compensated MASH cirrhosis. Forward-looking statements are subject to a number of risks and uncertainties including, but not limited to: the assumptions underlying the forward-looking statements; our ability to successfully commercialize Rezdiffra in the U.S. and Europe; risks related to obtaining and maintaining regulatory approvals, including, but not limited to, potential regulatory delays or rejections; our history of operating losses and the possibility that we may never achieve or maintain profitability; risks associated with meeting the objectives of our clinical trials, including, but not limited to our ability to achieve enrollment objectives concerning patient numbers (including an adequate safety database), outcomes objectives and/or timing objectives for our trials; any delays or failures in enrollment, and the occurrence of adverse safety events; risks related to the effects of Rezdiffra’s (resmetirom’s) mechanism of action or of any other product candidate; market demand for and acceptance of Rezdiffra; our ability to service indebtedness and otherwise comply with debt covenants; outcomes or trends from competitors; future topline data timing or results; our ability to prevent and/or mitigate cyber-attacks; our ability to protect our intellectual property rights; the uncertainties inherent in clinical testing; uncertainties concerning analyses or assessments outside of a controlled clinical trial; and changes in laws and regulations applicable to our business and our ability to comply with such laws and regulations. Undue reliance should not be placed on forward-looking statements, which speak only as of the date they are made. Madrigal undertakes no obligation to update any forward-looking statements to reflect new information, events, or circumstances after the date they are made, or to reflect the occurrence of unanticipated events. Please refer to Madrigal’s submissions filed with the U.S. Securities and Exchange Commission (SEC) for more detailed information regarding these risks and uncertainties and other factors that may cause actual results to differ materially from those expressed or implied. Madrigal specifically discusses these risks and uncertainties in greater detail in the sections appearing in Part 1A of its Annual Report on Form 10-K for the year ended December 31, 2025, and as updated from time to time by Madrigal’s other filings with the SEC.

Madrigal may use its website to comply with its disclosure obligations under Regulation FD. Therefore, investors should monitor Madrigal’s website in addition to following its press releases, filings with the SEC, public conference calls, and webcasts.

Madrigal Pharmaceuticals, Rezdiffra® and associated logos are trademarks of Madrigal Pharmaceuticals, Inc.

Investor Contact
Tina Ventura, [email protected]

Media Contact
Christopher Frates, [email protected]
2026-06-12 15:51 2mo ago
2026-06-02 21:40 3mo ago
Madrigal Pharmaceuticals Could Become The Next Vertex
MDGL Madrigal Pharmaceuticals
FMP Stock News
Original source text
Madrigal Pharmaceuticals, Inc. is a high-risk/high-reward play, focused solely on MASH with its first-in-class drug Rezdiffra. Rezdiffra's initial U.S. TAM is expanding, with diagnosis rates and label extensions potentially driving revenue to double-digit billions over the next decade. Competition from Novo Nordisk's Wegovy and upcoming Efruxifermin poses significant long-term risk, but MDGL enjoys a near-term lead and first-mover advantage.
2026-06-12 15:51 2mo ago
2026-06-03 08:00 3mo ago
Madrigal Pharmaceuticals to Participate in the 47th Annual Global Goldman Sachs Health Care Conference 2026
MDGL Madrigal Pharmaceuticals
FMP Stock News
Original source text
June 03, 2026 08:00 ET  | Source: Madrigal Pharmaceuticals, Inc.

CONSHOHOCKEN, Pa., June 03, 2026 (GLOBE NEWSWIRE) -- Madrigal Pharmaceuticals, Inc. (NASDAQ: MDGL) today announced that the company will participate in the 47th Annual Global Goldman Sachs Health Care Conference 2026 on Wednesday, June 10, 2026, at 11:20 A.M. EDT.

The presentation will be webcast live and may be accessed here or by visiting Madrigal’s Investor Relations Events and Presentations page. A replay of the webcast will be available after the event.

About Madrigal
Madrigal Pharmaceuticals, Inc. (Nasdaq: MDGL) is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a liver disease with high unmet medical need. Madrigal’s medication, Rezdiffra (resmetirom), is a once-daily, oral, liver-directed THR-β agonist designed to target key underlying causes of MASH. Rezdiffra was the first medication approved by both the FDA and European Commission for the treatment of MASH with moderate to advanced fibrosis (F2 to F3). An ongoing Phase 3 outcomes trial is evaluating Rezdiffra for the treatment of compensated MASH cirrhosis (F4c). For more information, visit www.madrigalpharma.com and follow us on LinkedIn.

Investor Contact
Tina Ventura, [email protected]

Media Contact
Christopher Frates, [email protected]
2026-06-12 15:51 2mo ago
2026-06-04 16:05 3mo ago
Madrigal Pharmaceuticals Announces Grants of Inducement Awards under Nasdaq Listing Rule 5635(c)(4)
MDGL Madrigal Pharmaceuticals
FMP Stock News
Original source text
June 04, 2026 16:05 ET  | Source: Madrigal Pharmaceuticals, Inc.

CONSHOHOCKEN, Pa., June 04, 2026 (GLOBE NEWSWIRE) -- Madrigal Pharmaceuticals, Inc. (NASDAQ: MDGL), a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), today announced that it granted equity awards on June 1, 2026 to 20 new non-executive employees as equity inducement awards under the terms of Madrigal’s 2025 Inducement Plan. The equity awards were approved by Madrigal’s independent Compensation Committee in accordance with Nasdaq Listing Rule 5635(c)(4).

The equity awards were granted as an inducement material to employees’ acceptance of employment with the company. The new employees received, in the aggregate, 6,881 time-based restricted stock units. All restricted stock units granted vest in four equal installments on each of the first through fourth anniversaries of the grant date. The vesting of all awards described above shall be subject to each such employee’s continued employment as of the applicable vesting date.

About Madrigal Pharmaceuticals

Madrigal Pharmaceuticals, Inc. (Nasdaq: MDGL) is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a liver disease with high unmet medical need. Madrigal’s medication, Rezdiffra (resmetirom), is a once-daily, oral, liver-directed THR-β agonist designed to target key underlying causes of MASH. Rezdiffra was the first medication approved by both the FDA and European Commission for the treatment of MASH with moderate to advanced fibrosis (F2 to F3). An ongoing Phase 3 outcomes trial is evaluating Rezdiffra for the treatment of compensated MASH cirrhosis (F4c). For more information, visit www.madrigalpharma.com.

Investor Contact
Tina Ventura, [email protected]

Media Contact
Christopher Frates, [email protected]
2026-06-12 15:51 2mo ago
2026-06-05 12:35 3mo ago
Madrigal (MDGL) Down 7.9% Since Last Earnings Report: Can It Rebound?
MDGL Madrigal Pharmaceuticals
FMP Stock News
Original source text
A month has gone by since the last earnings report for Madrigal (MDGL - Free Report) . Shares have lost about 7.9% in that time frame, underperforming the S&P 500.

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

Madrigal Q1 Earnings Beat, MASH Drug Sales Drive Top Line, Stock UpMadrigal reported first-quarter 2026 loss of $3.25 per share, narrower than the Zacks Consensus Estimate of a loss of $3.61. In the same quarter last year, the company had incurred a loss of $2.61 per share.

In the first quarter, MDGL generated total revenues of $311.3 million, up significantly year over year, entirely from product sales of Rezdiffra. The metric beat the Zacks Consensus Estimate of $301 million. Rezdiffra is the first marketed drug in MDGL’s portfolio and posted significant year-over-year growth, driven by increased demand.

MDGL’s Q4 Results in DetailIn March 2024, the FDA granted accelerated approval to Rezdiffra, making it the first and currently the only approved therapy for the MASH indication. The eligible patient population includes adults with noncirrhotic MASH with moderate to advanced liver fibrosis. Rezdiffra has also received conditional approval as the first and only therapy in the EU to treat adults with noncirrhotic MASH with moderate-to-advanced liver fibrosis. Per Madrigal, more than 42,250patients are receiving the treatment as of March 31, 2026, up 2.5 times from first-quarter 2025, reflecting continued strong physician adoption and high patient demand.

During the quarter, research and development expenses more than doubled to $108.7 million in the first quarter of 2026. The massive increase can be primarily attributed to one-time, upfront business development expenses of $54.3 million.

Selling, general and administrative expenses also nearly doubled in the reported quarter to $268.5 million. This exponential rise was on account of increased commercial launch activities for Rezdiffra, including significant increases in headcount to support marketing efforts.

Madrigal had cash, cash equivalents and marketable securities worth $817.9 million as of March 31, 2026, compared with $988.6 million as of Dec. 31, 2025.

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

The consensus estimate has shifted -68.41% due to these changes.

VGM ScoresAt this time, Madrigal has a average Growth Score of C, though it is lagging a lot on the Momentum Score front with an F. Charting a somewhat similar path, the stock was allocated a grade of D on the value side, putting it in the bottom 40% for this investment strategy.

Overall, the stock has an aggregate VGM Score of F. 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 these revisions indicates a downward shift. Notably, Madrigal has a Zacks Rank #3 (Hold). We expect an in-line return from the stock in the next few months.
2026-06-12 15:51 2mo ago
2026-06-10 14:22 3mo ago
Madrigal Pharmaceuticals, Inc. (MDGL) Presents at Goldman Sachs 47th Annual Global Healthcare Conference 2026 Transcript
MDGL Madrigal Pharmaceuticals
FMP Stock News
Original source text
Madrigal Pharmaceuticals, Inc. (MDGL) Presents at Goldman Sachs 47th Annual Global Healthcare Conference 2026 Transcript
2026-06-12 15:51 2mo ago
2026-05-05 14:08 4mo ago
Live Nation to Report First Earnings Since Monopoly Ruling
LYV Live Nation Entertainment
FMP Stock News
Original source text
Ticketmaster's parent company is scheduled to report first-quarter financial results after the stock market closes Tuesday.
2026-06-12 15:51 2mo ago
2026-05-05 16:10 4mo ago
LIVE NATION ENTERTAINMENT REPORTS FIRST QUARTER 2026 RESULTS
LYV Live Nation Entertainment
FMP Stock News
Original source text
Q1'26 Banner Image , /PRNewswire/ --

"2026 is off to a powerful start, with first quarter revenue climbing 12% to $3.8 billion. In an increasingly digital and AI-driven world, the global desire for authentic human connection has never been stronger. We are seeing a fundamental shift as fans prioritize the 'live' experience—the chance to be physically present with their favorite artists and share that energy with friends and fellow fans in a way a screen simply cannot replicate.

This cultural demand is driving record-breaking activity across our business. We have already booked over 85% of our large-venue shows for the year, with show counts up year-over-year across stadiums, arenas, and amphitheaters. Our momentum is clear: we have sold over 107 million tickets to date—an 11% increase—and Venue Nation is on track to grow fan attendance at our owned and operated venues by double-digits. As we continue to expand our global footprint to meet this growing demand for physical connection, we are well positioned for long-term compounding double-digit growth." –Michael Rapino, President and CEO

LIVE NATION PACES FOR DOUBLE-DIGIT GROWTH IN 2026 (1Q26 vs. 1Q25)

Revenue of $3.8 billion, up 12% Operating loss of $371 million, impacted by a $450 million legal accrual Adjusted operating income (AOI) of $371 million, up 9% with operating strength across all segments: Concerts AOI of $3 million with fan attendance of 24 million, up 7% Ticketing AOI of $256 million, driven by 81 million fee-bearing tickets, up 4% Sponsorship AOI up 21% to $165 million, driven by brand demand to connect with our global fan base Q1 deferred revenue for Concerts and Ticketmaster at record levels: Event-related deferred revenue of $6.6 billion, up 22%—largest deferred revenue balance in company history Ticketing deferred revenue of $368 million, up 29%, accounting for $5.5 billion in deferred ticketing gross transaction value (GTV) While 2026 operating income will be impacted by a $450 million legal accrual, on pace to grow adjusted operating income by double-digits this year GLOBAL ARTIST AND TOURING MOMENTUM ACCELERATE 2026 CONCERTS PERFORMANCE 

Revenue of $2.8 billion, up 12% vs. 1Q25 Q1 AOI of $3 million and $12 million on a constant currency basis Over 85% of 2026 large venue shows booked (confirmed and offer-in) through the end of April, pacing up high-single digits so far this year, with stadium, arena, and amphitheater show count all up year-on-year Tickets sold through the end of April for 2026 Live Nation concerts up 11% to over 107 million, with consistent double-digit growth across key venue types—stadiums, arenas, amphitheaters, and festivals Full year fan attendance projected to grow high-single digits with timing shifts due to venue mix: Top driver of Q2 fan growth expected to be third-party arenas 70% of amphitheater fan growth expected to occur in Q3, in line with the summer calendar All stadium fan growth will occur in the second half For the full year, Concerts on track to deliver double-digit AOI growth with margins positioned to build on last year's VENUE NATION EXPANDS GLOBAL FOOTPRINT AND DELIVERS DEEPER FAN ENGAGEMENT 

Venues opened in 2025 on track to reach their run-rate annual AOI across Concerts and Sponsorship by 2028, delivering 20%+ IRRs: TD Coliseum in Hamilton, Canada delivered a strong Q1 with show count up double-digits and set to deliver 80 shows for the full year—surpassing initial projections At Rogers Stadium in Toronto, projected show count for the full-year is up 40% compared to its inaugural year in 2025 Ongoing roll out of premium hospitality, Live Nation's Vinyl Room, delivering strong results so far this year with onsite spending at the Hollywood Palladium over $100 per fan, and up 30% per fan at Ziggo Dome in Amsterdam Venue Nation on track to grow fans at owned or operated venues by double-digits in 2026: Recently completed three acquisitions: Movistar Arena Santiago, Unipol Forum in Milan, and IMPACT Arena in Bangkok, with a cumulative annual fan capacity of approximately four million 2026 major projects include two U.S. amphitheaters and one stadium in Guadalajara, Mexico 2026 preopening costs for all venues under development expected to remain at approximately $50 million Venues opening in 2026 are projected to reach their run-rate annual AOI across Concerts and Sponsorship by 2029, continuing to deliver 20%+ IRRs CONCERTS DEMAND DRIVES TICKETMASTER STRENGTH IN Q1 (vs. 1Q25 unless otherwise noted)

Revenue of $765 million, up 10% AOI of $256 million, up 1% $30 million in expenses related to legal and operational improvements Primary GTV grew 14%, with concerts delivering most of the growth Ticketmaster well positioned for sustained long-term growth: Ticketmaster total fee-bearing tickets transacted through April for 2026 up 9% to 138 million, with GTV of $17 billion, up 15% Primary fee-bearing ticket volume expected to grow mid-single digits for the full year  Ongoing efforts to reduce scalper activity expected to impact full-year Ticketmaster AOI by mid-single digits Full year AOI margin expected to be similar to last year THE POWER OF PRESENCE: BRANDS PRIORITIZE AUTHENTIC CONNECTION AS GLOBAL SPONSORSHIP ACTIVITY REACHES NEW HEIGHTS (vs. 1Q25 unless otherwise noted)

Revenue of $259 million, up 20% AOI of $165 million, up 21%, reflecting the strength of international festivals in South America and our growing venue portfolio 85% of 2026 sponsorship commitments booked as of end of April, up double-digits AOI expected to grow double-digits for the full year, driven by venue portfolio expansion including naming rights across major arenas and festivals globally Full year AOI margin expected to be similar to last year CAPITAL ALLOCATION SUPPORTS VENUE EXPANSION AND LONG-TERM GROWTH 

Q1 capital expenditures totaled $249 million; full year spend expected to be $1.1 to $1.2 billion:  Approximately $800 to $850 million of total capex is for venue expansion and enhancement projects Venue investment cash requirements expected to be reduced by approximately $250 million from funding by joint-venture partners, sponsorship agreements, and other sources Additional capex allocated to our ticketing and sponsorship growth initiatives, as well as ongoing maintenance at our venues Full year AOI to free cash flow—adjusted conversion expected to be in line with or higher than 2025 CONTINUED TO BOLSTER OUR BALANCE SHEET IN Q1

Cash and cash equivalents of $9.1 billion, up from $7.2 billion last year and free cash of $1.7 billion, up from $1.1 billion last year Leverage stands at 3.6x, in line with historical levels, with a weighted average cost of debt of 4.2% In April, raised approximately €610 million in long-term debt at 5.5% through an investment grade financing vehicle backed by a portfolio of major venues FULL-YEAR INCOME STATEMENT DETAILS (vs. FY25)

Depreciation and amortization expected to grow 12-15% Net interest expense is expected to be $280 million Income tax expense is expected to be 15-20% of AOI, with cash taxes projected to be 80% of that amount Below the line items: A $450 million legal accrual impacted Q1 operating income and earnings per share by $(1.93) Noncontrolling interest expense is expected to grow 25% driven by strong performance across our global partnerships Accretion expense is expected to be $160-180 million 2026 share count not expected to change materially from 2025 Compare Our Operating Results to Past Quarters In The Trended Results Grid:
https://investors.livenationentertainment.com/financial-information/financial-results

The company will webcast a teleconference today, May 5, 2026, at 2:00 p.m. Pacific Time to discuss its financial performance, operational matters and potentially other material developments. Interested parties should visit the "News / Events" section of the company's website at investors.livenationentertainment.com to listen to the webcast. Supplemental statistical and financial information to be provided on the call, if any, will be posted to the "Financial Info" section of the website. A replay of the webcast will also be available on the Live Nation website. The link to the 1Q26 Trended Results Grid is provided above for convenience and such grid is not a part of, or incorporated into, this press release or any SEC filings that include this press release.

Notice Regarding Financial Statements
The company has provided certain financial statements at the end of this press release for reference. These financial statements should be read in conjunction with the full financial statements, and the notes thereto, set forth in the company's Annual Report on Form 10-Q for the quarter ended March 31, 2026 to be filed with the Securities and Exchange Commission today and available on the SEC's website at sec.gov.

About Live Nation Entertainment:
Live Nation Entertainment, Inc. (NYSE: LYV) is the world's leading live entertainment company comprised of global market leaders: Ticketmaster, Live Nation Concerts, and Live Nation Media & Sponsorship. For additional information, visit investors.livenationentertainment.com.

FINANCIAL HIGHLIGHTS – FIRST QUARTER

(unaudited; $ in millions)

Q1 2026
Reported

Q1 2025

Reported

Change

Q1 2026

Currency
Impacts

Q1 2026
Constant
Currency

Change at
Constant
Currency

Revenue

Concerts

$      2,775.5

$       2,484.1

12 %

$     (89.9)

$      2,685.6

8 %

Ticketing

765.0

694.7

10 %

(19.0)

746.0

7 %

Sponsorship & Advertising

258.6

216.1

20 %

(12.3)

246.3

14 %

Other and Eliminations

(6.1)

(12.8)

*

0.0

(6.1)

*

$      3,793.0

$       3,382.1

12 %

$    (121.2)

$      3,671.8

9 %

Consolidated Operating

Income (Loss)

$       (370.5)

$         114.8

*

$       12.7

$       (357.8)

*

Adjusted Operating Income (Loss)

Concerts

$           2.9

$            6.6

(56) %

$        8.9

$          11.8

79 %

Ticketing

255.6

253.1

1 %

(6.6)

249.0

(2) %

Sponsorship & Advertising

164.6

136.0

21 %

(9.5)

155.1

14 %

Other and Eliminations

(4.2)

(5.9)

*

0.1

(4.1)

*

Corporate

(47.9)

(48.7)

2 %

0.0

(47.9)

2 %

$        371.0

$         341.1

9 %

$       (7.1)

$        363.9

7 %

* Percentages are not meaningful

Reconciliation of Operating Income (Loss) to Adjusted Operating Income

(unaudited; $ in millions)

Q1 2026

Q1 2025

Operating Income (Loss)

$            (370.5)

$              114.8

Acquisition expenses

69.4

29.7

Amortization of non-recoupable ticketing contract advances

26.0

24.7

Depreciation and amortization

169.3

149.5

Gain on sale of operating assets

(6.0)

(2.2)

Governmental Investigations and Litigation

450.0



Stock-based compensation expense

32.8

24.6

Adjusted Operating Income

$             371.0

$              341.1

Reconciliations of Certain Non-GAAP Measures to Their Most Directly Comparable GAAP Measures

(unaudited; $ in millions)

Reconciliation of Free Cash Flow — Adjusted to Net Cash Provided by Operating Activities

Q1 2026

Q1 2025

Net cash provided by operating activities

$            2,338.8

$            1,321.3

Changes in operating assets and liabilities (working capital)

(2,546.1)

(1,056.6)

Governmental Investigations and Litigation

450.0



Free cash flow from earnings

$              242.7

$              264.7

Less: Maintenance capital expenditures

(30.0)

(14.9)

          Distributions to noncontrolling interests

(38.0)

(33.7)

Free cash flow — adjusted

$              174.7

$              216.1

Net cash used in investing activities

$             (417.7)

$             (217.4)

Net cash provided by (used in) financing activities

$              117.5

$             (173.2)

Reconciliation of Free Cash to Cash and Cash Equivalents

($ in millions)

March 31,
2026

March 31,
2025

Cash and cash equivalents

$               9,077.8

$               7,158.7

Short-term investments

43.8

64.5

Client cash

(1,810.8)

(1,559.9)

Deferred revenue — event-related

(6,601.7)

(5,395.9)

Accrued artist fees

(173.8)

(125.5)

Collections on behalf of others

(164.5)

(140.5)

Prepaid expenses — event-related

1,336.6

1,117.5

Free cash

$               1,707.4

$               1,118.9

Forward-Looking Statements, Non-GAAP Financial Measures and Reconciliations:

Certain statements in this press release constitute "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements include, but are not limited to statements regarding the company's prospects for a record year in 2026 with anticipated double-digit growth, and its positioning for long-term compounding double-digit growth; expectations for operating income and adjusted operating income levels in 2026; expected Venue Nation fan growth at owned or operated venues in 2026; anticipated full year adjusted operating income growth for the company's concerts business, as well as expected full year fan attendance and anticipated shifts in seasonality by venue type, and full year margin expectations; pacing for venues opened in 2025 to reach their run-rate annual adjusted operating income across concerts and sponsorship by 2028 as well as expected IRRs, as well as expectations for show count at these venues; expectations for Venue Nation fan growth at owned or operated venues for 2026 versus 2025; expected 2026 Venue Nation new builds; anticipated 2026 preopening costs for venues under development; the projection that venues opening in 2026 will reach their run-rate annual adjusted operating income across concerts and sponsorship by 2029, as well as expected IRRs; Ticketmaster's positioning for sustained long-term growth, including full year expectations for growth in primary fee-bearing tickets, the impact to full year adjusted operating income from ongoing efforts to reduce scalper activity, and full year 2026 adjusted operating income margin expectations; expectations for full year 2026 adjusted operating income growth in the company's sponsorship & advertising business, as well as full year adjusted operating income margin for the business; expected capital expenditure levels in 2026; expectations for full year 2026 adjusted operating income to free cash flow—adjusted conversion rates; expectations for full year 2026 levels of depreciation and amortization, net interest expense, income tax expense as a percentage of adjusted operating income, accretion expense, noncontrolling interest expense, and share count.

Live Nation wishes to caution you that there are some known and unknown factors that could cause actual results to differ materially from any future results, performance or achievements expressed or implied by such forward-looking statements, including but not limited to operational challenges in achieving strategic objectives and executing on the company's plans, the risk that the company's markets do not evolve as anticipated, the potential impact of any economic slowdown and operational challenges associated with selling tickets and staging events.

Live Nation refers you to the documents it files from time to time with the U.S. Securities and Exchange Commission, or SEC, specifically the section titled "Item 1A. Risk Factors" of the company's most recent Annual Report filed on Form 10-K, and Quarterly Reports on Form 10-Q and its Current Reports on Form 8-K, which contain and identify other important factors that could cause actual results to differ materially from those contained in the company's projections or forward-looking statements. You are cautioned not to place undue reliance on these forward-looking statements which speak only as of the date on which they are made. All subsequent written and oral forward-looking statements by or concerning Live Nation are expressly qualified in their entirety by the cautionary statements above. Live Nation does not undertake any obligation to publicly update or revise any forward-looking statements because of new information, future events or otherwise.

This press release contains certain non-GAAP financial measures as defined by SEC Regulation G. A reconciliation of each such measure to its most directly comparable GAAP financial measure, together with an explanation of why management believes that these non-GAAP financial measures provide useful information to investors, is provided herein.

Adjusted Operating Income (Loss), or AOI, is a non-GAAP financial measure that we define as operating income (loss) before certain acquisition expenses (including ongoing legal costs stemming from the Ticketmaster merger, changes in the fair value of accrued acquisition-related contingent consideration obligations, and acquisition-related severance and compensation), amortization of non-recoupable ticketing contract advances, depreciation and amortization (including goodwill impairment), loss (gain) on disposal of operating assets, and stock-based compensation expense. Due to the significant and non-recurring nature of the matters, we also exclude from AOI the impact of realized liabilities for settlements and expenses for regulatory compliance matters associated with the provision for losses arising from certain significant governmental investigations and litigations under ASC 450 - Contingencies, which are described under the heading "Governmental Investigations and Litigation" in Note 6 of the Notes to the Consolidated Financial Statements in our Quarterly Report on Form 10-Q for the quarter ended March 31, 2026. Except as described above, ongoing legal costs associated with defense of these claims, such as attorney fees, are not excluded from AOI. We use AOI to evaluate the performance of our operating segments. We believe that information about AOI assists investors by allowing them to evaluate changes in the operating results of our portfolio of businesses separate from non-operational factors that affect net income (loss), thus providing insights into both operations and the other factors that affect reported results. AOI is not calculated or presented in accordance with GAAP. A limitation of the use of AOI as a performance measure is that it does not reflect the periodic costs of certain amortizing assets used in generating revenue in our business. Accordingly, AOI should be considered in addition to, and not as a substitute for, operating income (loss), net income (loss), and other measures of financial performance reported in accordance with GAAP. Furthermore, this measure may vary among other companies; thus, AOI as presented herein may not be comparable to similarly titled measures of other companies.

AOI margin is a non-GAAP financial measure that we calculate by dividing AOI by revenue. We use AOI margin to evaluate the performance of our operating segments. We believe that information about AOI margin assists investors by allowing them to evaluate changes in the operating results of our portfolio of businesses separate from non-operational factors that affect net income (loss), thus providing insights into both operations and the other factors that affect reported results. AOI margin is not calculated or presented in accordance with GAAP. A limitation of the use of AOI margin as a performance measure is that it does not reflect the periodic costs of certain amortizing assets used in generating revenue in our business. Accordingly, AOI margin should be considered in addition to, and not as a substitute for, operating income (loss) margin, and other measures of financial performance reported in accordance with GAAP. Furthermore, this measure may vary among other companies; thus, AOI margin as presented herein may not be comparable to similarly titled measures of other companies.

Constant Currency is a non-GAAP financial measure when applied to a GAAP financial measure. We calculate currency impacts as the difference between current period activity translated using the current period's currency exchange rates and the comparable prior period's currency exchange rates. We present constant currency information to provide a framework for assessing how our underlying businesses performed excluding the effect of foreign currency rate fluctuations.

Free Cash Flow — Adjusted, or FCF, is a non-GAAP financial measure that we define as net cash provided by (used in) operating activities less changes in operating assets and liabilities, less maintenance capital expenditures, less distributions to noncontrolling interest partners. We use FCF among other measures, to evaluate the ability of operations to generate cash that is available for purposes other than maintenance capital expenditures. We believe that information about FCF provides investors with an important perspective on the cash available to service debt, make acquisitions, and for revenue generating capital expenditures. FCF is not calculated or presented in accordance with GAAP. A limitation of the use of FCF as a performance measure is that it does not necessarily represent funds available for operations and is not necessarily a measure of our ability to fund our cash needs. Accordingly, FCF should be considered in addition to, and not as a substitute for, net cash provided by (used in) operating activities and other measures of financial performance reported in accordance with GAAP. Furthermore, this measure may vary among other companies; thus, FCF as presented herein may not be comparable to similarly titled measures of other companies.

Free Cash is a non-GAAP financial measure that we define as cash and cash equivalents less ticketing-related client funds, less event-related deferred revenue, less accrued expenses due to artists and cash collected on behalf of others, plus event-related prepaids. We use free cash as a proxy for how much cash we have available to, among other things, optionally repay debt balances, make acquisitions and fund revenue generating capital expenditures. Free cash is not calculated or presented in accordance with GAAP. A limitation of the use of free cash as a performance measure is that it does not necessarily represent funds available from operations and it is not necessarily a measure of our ability to fund our cash needs. Accordingly, free cash should be considered in addition to, and not as a substitute for, cash and cash equivalents and other measures of financial performance reported in accordance with GAAP. Furthermore, this measure may vary among other companies; thus, free cash as presented herein may not be comparable to similarly titled measures of other companies.

LIVE NATION ENTERTAINMENT, INC.

CONSOLIDATED BALANCE SHEETS

(unaudited)

March 31,
2026

December 31,
2025

(in thousands)

ASSETS

Current assets

    Cash and cash equivalents

$          9,077,847

$          7,094,200

    Accounts receivable, less allowance of $78,255 and $73,912, respectively

1,965,296

2,009,055

    Prepaid expenses

2,217,054

1,453,732

    Other current assets

381,342

417,405

Total current assets

13,641,539

10,974,392

Property, plant and equipment, net

3,664,231

3,415,771

Operating lease assets

1,910,332

1,869,753

Intangible assets

    Definite-lived intangible assets, net

1,071,290

1,078,453

    Indefinite-lived intangible assets, net

368,961

369,015

Goodwill

2,933,243

2,889,178

Long-term advances

667,912

631,071

Other long-term assets

1,810,584

1,684,900

Total assets

$         26,068,092

$         22,912,533

LIABILITIES AND EQUITY

Current liabilities

    Accounts payable, client accounts

$          2,174,981

$          1,941,389

    Accrued expenses and accounts payable

3,562,342

3,555,811

    Deferred revenue

7,410,720

4,461,959

    Current portion of long-term debt, net

1,800,776

587,630

    Other current liabilities

467,757

482,061

Total current liabilities

15,416,576

11,028,850

Long-term debt, net

6,709,420

7,612,018

Long-term operating lease liabilities

2,073,207

2,036,974

Other long-term liabilities

435,347

415,844

Commitments and contingent liabilities

Redeemable noncontrolling interests

951,724

924,472

Stockholders' equity

    Common stock

2,333

2,328

    Additional paid-in capital

1,405,279

1,455,925

    Accumulated deficit

(1,431,082)

(1,041,978)

    Cost of shares held in treasury

(30,396)

(30,396)

    Accumulated other comprehensive loss

(85,538)

(114,872)

Total Live Nation stockholders' equity

(139,404)

271,007

Noncontrolling interests

621,222

623,368

Total equity

481,818

894,375

Total liabilities and equity

$         26,068,092

$         22,912,533

LIVE NATION ENTERTAINMENT, INC.

CONSOLIDATED STATEMENTS OF OPERATIONS

(unaudited)

Three Months Ended March 31,

2026

2025

(in thousands except share and

per share data)

Revenue

$           3,793,029

$           3,382,117

Operating expenses:

Direct operating expenses

2,478,458

2,254,937

Selling, general and administrative expenses

961,519

778,922

Depreciation and amortization

169,296

149,455

Gain on disposal of operating assets

(6,022)

(2,202)

Corporate expenses

560,294

86,236

Operating income (loss)

(370,516)

114,769

Interest expense

90,522

80,343

Interest income

(39,467)

(34,061)

Equity in losses (earnings) of nonconsolidated affiliates

2,883

(479)

Other expense (income), net

(12,351)

2,953

Income (loss) before income taxes

(412,103)

66,013

Income tax expense (benefit)

(32,085)

19,711

Net income (loss)

(380,018)

46,302

Net income attributable to noncontrolling interests

9,086

23,099

Net income (loss) attributable to common stockholders of Live Nation

$            (389,104)

$               23,203

Basic and diluted net loss per common share available

to common stockholders of Live Nation

$                (1.85)

$                (0.32)

Weighted average common shares outstanding:

Basic and diluted

232,400,991

231,220,841

Reconciliation to net loss available to common stockholders of Live Nation:

Net income (loss) attributable to common stockholders of Live Nation

$            (389,104)

$               23,203

Accretion of redeemable noncontrolling interests

(41,279)

(98,094)

Net loss available to common stockholders of Live Nation—basic and diluted

$            (430,383)

$             (74,891)

LIVE NATION ENTERTAINMENT, INC.

CONSOLIDATED STATEMENTS OF CASH FLOWS

(unaudited)

Three Months Ended March 31,

2026

2025

(in thousands)

CASH FLOWS FROM OPERATING ACTIVITIES

Net income (loss)

$        (380,018)

$          46,302

Reconciling items:

Depreciation

99,565

89,462

Amortization of definite-lived intangibles

69,731

59,993

Amortization of non-recoupable ticketing contract advances

26,020

24,722

Deferred income taxes

(44,693)

4,271

Amortization of debt issuance costs and discounts

5,150

3,684

Stock-based compensation expense

32,777

24,550

Unrealized changes in fair value of contingent consideration

10,409

1,169

Equity in losses of nonconsolidated affiliates, net of distributions

4,553

3,480

Provision for uncollectible accounts receivable

(1,224)

3,574

Gain on mark-to-market of investments in nonconsolidated affiliates and crypto assets

(6,189)

(5,467)

Loss (gain) on forward currency exchange contracts

(17,306)

13,361

Other, net

(6,002)

(4,485)

Changes in operating assets and liabilities, net of effects of acquisitions and dispositions:

Decrease (increase) in accounts receivable

70,629

(70,535)

Increase in prepaid expenses and other assets

(783,967)

(592,946)

Increase (decrease) in accrued expenses, accounts payable and other liabilities

281,040

(545,945)

Increase in deferred revenue

2,978,360

2,266,061

Net cash provided by operating activities

2,338,835

1,321,251

CASH FLOWS FROM INVESTING ACTIVITIES

Advances of notes receivable

(1,944)

(6,403)

Collections of notes receivable

5,920

9,375

Investments made in nonconsolidated affiliates

(9,649)

(3,887)

Purchases of property, plant and equipment

(308,978)

(170,791)

Cash paid for acquisition of right-of-use assets



(20,800)

Cash paid for acquisitions, net of cash acquired

(113,203)

(31,346)

Other, net

10,115

6,457

Net cash used in investing activities

(417,739)

(217,395)

CASH FLOWS FROM FINANCING ACTIVITIES

Proceeds from debt, net of debt issuance costs

226,161

11,059

Payments on debt including extinguishment costs

(6,611)

(86,828)

Contributions from noncontrolling interests

11,349

4,612

Distributions to noncontrolling interests

(38,000)

(33,742)

Purchases of noncontrolling interests, net

(25,882)

(4,496)

Proceeds from exercise of stock options

783

2,606

Taxes paid for net share settlement of equity awards

(47,930)

(65,009)

Payments for deferred and contingent consideration

(1,530)

(1,242)

Other, net

(859)

(150)

Net cash provided by (used in) financing activities

117,481

(173,190)

Effect of exchange rate changes on cash, cash equivalents and restricted cash

(54,613)

131,471

Net increase in cash, cash equivalents and restricted cash

1,983,964

1,062,137

Cash, cash equivalents and restricted cash at beginning of period

7,106,986

6,106,109

Cash, cash equivalents and restricted cash at end of period

$       9,090,950

$       7,168,246

SOURCE Live Nation Entertainment
2026-06-12 15:51 2mo ago
2026-05-05 16:16 4mo ago
Live Nation posts upbeat quarterly revenue on steady demand for concerts
LYV Live Nation Entertainment
FMP Stock News
Original source text
A Live Nation sign and office building stand along Hollywood Blvd, in Los Angeles, California, U.S., May 23, 2024. REUTERS/Mike Blake Purchase Licensing Rights, opens new tab

May 5 (Reuters) - Live Nation Entertainment (LYV.N), opens new tab beat analysts' estimates for first-quarter revenue on Tuesday, underscoring steady demand for concerts and live ​events even as the Ticketmaster parent faces mounting ‌regulatory and legal scrutiny.

It posted quarterly revenue of $3.8 billion, above analysts' estimates of $3.57 billion, according to data compiled by LSEG.

The Reuters Inside Track newsletter is your essential guide during the World Cup. Sign up here.

Demand for live ​music has remained resilient as fans prioritize spending on ​experiences despite broader economic uncertainty.

Live Nation, the world's ⁠largest concert promoter, has leaned on blockbuster tours by ​major artists and higher ticket prices to drive growth.

"We have ​already booked over 85% of our large-venue shows for the year, with show counts up year-over-year across stadiums, arenas, and amphitheaters," Live Nation ​CEO Michael Rapino said.

The results come as Live Nation is ​under increasing pressure from U.S. regulators and lawmakers over competition concerns in ‌the ⁠live events industry.

Last month, a New York jury found that Live Nation holds illegal monopolies in the market for ticketing services to more than 200 major concert venues, and the ​market for dozens ​of large ⁠concert amphitheaters booked by artists.

Tickets sold through the end of April for 2026 Live Nation ​concerts were up 11% to over 107 million.

The ​company ⁠posted operating loss of $371 million, impacted by a $450 million legal accrual, and cautioned that 2026 operating income will be affected ⁠by ​the charge.

It reported a loss of $1.85 ​per share, compared with a loss of 32 cents per share a year ​earlier.

Reporting by Kritika Lamba in Bengaluru; Editing by Sahal Muhammed

Our Standards: The Thomson Reuters Trust Principles., opens new tab
2026-06-12 15:51 2mo ago
2026-05-05 17:27 4mo ago
Live Nation Swings to Loss Due to Legal Fees; Revenue Climbs on Concert Demand
LYV Live Nation Entertainment
FMP Stock News
Original source text
The company posted a first-quarter loss of $389.1 million, compared with a profit of $23.2 million a year earlier.
2026-06-12 15:51 2mo ago
2026-05-05 19:00 4mo ago
Live Nation (LYV) Q1 Earnings: Taking a Look at Key Metrics Versus Estimates
LYV Live Nation Entertainment
FMP Stock News
Original source text
Although the revenue and EPS for Live Nation (LYV) give a sense of how its business performed in the quarter ended March 2026, it might be worth considering how some key metrics compare with Wall Street estimates and the year-ago numbers.
2026-06-12 15:50 2mo ago
2026-05-05 19:10 4mo ago
Live Nation (LYV) Reports Q1 Loss, Beats Revenue Estimates
LYV Live Nation Entertainment
FMP Stock News
Original source text
Live Nation (LYV) came out with a quarterly loss of $0.32 per share versus the Zacks Consensus Estimate of a loss of $0.27. This compares to a loss of $0.32 per share a year ago.
2026-06-12 15:50 2mo ago
2026-05-05 19:31 4mo ago
Live Nation Entertainment, Inc. (LYV) Q1 2026 Earnings Call Transcript
LYV Live Nation Entertainment
FMP Stock News
Original source text
Live Nation Entertainment, Inc. (LYV) Q1 2026 Earnings Call Transcript
2026-06-12 15:50 2mo ago
2026-05-06 16:46 4mo ago
Why Live Nation Entertainment Stock Jumped 7% Today
LYV Live Nation Entertainment
FMP Stock News
Original source text
Live Nation Entertainment (LYV 0.25%) earned an encore on Wednesday. The Ticketmaster parent technically posted a mixed earnings report, hampered by a large legal expense. Investors applauded the results anyway, as management expects stronger profits in the upcoming quarters.

The stock closed Wednesday's trading at a 6.7% gain. It reached a peak of 8% near noon ET.

Today's Change

(

-0.25

%) $

-0.43

Current Price

$

171.90

Live Nation's Q1 by the numbers Q1 revenues rose 12% year-over-year to $3.8 billion. The analyst community had expected roughly $3.6 billion.

On the bottom line, Live Nation's net losses deepened from $0.32 to $1.85 per share, well below the Street estimate of $0.36 per share. However, these generally accepted accounting practices (GAAP) figures include a $450 million charge for legal fees. The company doesn't publish adjusted earnings figures, but if I do the math myself, Live Nation would have seen positive earnings of approximately $0.08 per share without those costly legal fees.

Image source: Getty Images.

Legal drama aside, ticket sales look strong Mind you, Live Nation hasn't entirely closed the books on that large legal expense. The company has appealed several pieces of the underlying jury verdict, so the lawsuit that the Department of Justice launched in May 2024 is still in play.

Looking beyond the courtroom drama, Live Nation sees healthy concert ticket sales as the summer season draws near. In particular, the low-priced amphitheater format is off to a strong start, which makes sense in this era of budget-pinching inflation.

"Consumers still consider the live show very important in their social calendar for the year," CEO Michael Rapino said on the earnings call. "We have seen broad, strong demand across the board."

With ticket sales up double digits and most large-venue shows already booked for 2026, Live Nation's core business appears healthy. The legal saga may drag on, but investors seem willing to look past it for now.

Anders Bylund has no position in any of the stocks mentioned. The Motley Fool recommends Live Nation Entertainment. The Motley Fool has a disclosure policy.
2026-06-12 15:50 2mo ago
2026-05-07 14:08 4mo ago
Ticketmaster Lays Off 8% Of Workforce Following Live Nation Q1 Report
LYV Live Nation Entertainment
FMP Stock News
Original source text
LYV stock is moving lower. See the chart and price action here. The layoffs primarily hit engineering, product and design roles, with contractors also reduced, according to Pollstar.

Ticketmaster Global President Saumil Mehta said the cuts were aimed at "stronger prioritization," including flattening layers, consolidating ownership and putting more energy behind specific initiatives.

The timing is notable because the reductions came just after Live Nation reported first-quarter results showing continued demand for concerts and ticketing.

Live Nation posted Q1 revenue of $3.79 billion, ahead of consensus estimates of $3.57 billion, for a revenue beat of $221.8 million, according to Benzinga Pro data.

Still, the company reported a Q1 operating loss of $370.5 million and diluted EPS of negative $1.85.

Live Nation said its results were impacted by a $450 million legal accrual related to government investigations and litigation.

Ticketmaster itself remained a bright spot in the quarter. Live Nation said Ticketing revenue rose 10% year-over-year to $765 million, while Ticketmaster fee-bearing tickets transacted through April rose 9% to 138 million and gross transaction value increased 15% to $17 billion.

Management framed the layoffs as a forward-looking move rather than a reaction to weak results. Mehta told Pollstar the strong performance reflected the past, while the cuts were designed to position Ticketmaster for the next 12 to 24 months.

LYV Price Action: Live Nation Entertainment shares were down 3.03% at $162.74 at the time of publication Thursday, according to Benzinga Pro.

Over the past month, LYV has gained about 5.1% versus a 11.3% rise in the S&P 500 and is up roughly 18% year-to-date compared to the index’s 6.6% gain.

Photo: Shutterstock

This content was partially produced with the help of AI tools and was reviewed and published by Benzinga editors.

Market News and Data brought to you by Benzinga APIs

© 2026 Benzinga.com. Benzinga does not provide investment advice. All rights reserved.

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2026-06-12 15:50 2mo ago
2026-05-11 08:05 4mo ago
Live Nation Entertainment Q1 Earnings Call Highlights
LYV Live Nation Entertainment
FMP Stock News
Original source text
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2026-06-12 15:50 2mo ago
2026-05-14 14:10 3mo ago
Live Nation Entertainment, Inc. (LYV) Presents at MoffettNathanson's Media, Internet & Communications Conference Transcript
LYV Live Nation Entertainment
FMP Stock News
Original source text
Live Nation Entertainment, Inc. (LYV) Presents at MoffettNathanson's Media, Internet & Communications Conference Transcript
2026-06-12 15:50 2mo ago
2026-05-20 15:00 3mo ago
Live Nation Entertainment, Inc. (LYV) Presents at J.P. Morgan 54th Annual Global Technology, Media and Communications Conference Transcript
LYV Live Nation Entertainment
FMP Stock News
Original source text
Live Nation Entertainment, Inc. (LYV) Presents at J.P. Morgan 54th Annual Global Technology, Media and Communications Conference Transcript
2026-06-12 15:50 2mo ago
2026-05-23 08:00 3mo ago
‘Blue dot fever'? What's really behind a tricky summer dynamic for live music
LYV Live Nation Entertainment
FMP Stock News
Original source text
This summer, mega artist Harry Styles will take the stage at Madison Square Garden in New York City for an exclusive 30-show residency – his only planned stop in the country and a show that's garnered intense attention since its announcement.

Despite her best efforts, Shira Elfassy won't be there.

"His tickets were absurd," Elfassy, 29, told CNBC. "It felt like an insult going in and seeing, like, not only can I not get in, not only are there no tickets left, but even then, the most basic price point is $500 for a nose-bleed seat — and this is becoming commonplace."

Instead, Elfassy said she got tickets to see other artists live, like Florence + the Machine and Olivia Rodrigo, at far lower price points. She said feeling "priced out" of some concerts is now a common occurrence.

"It's just a weird dynamic now. ... At this point, if I have to make the decision between making more summer plans or hanging out with my friends — or even just [to] pay rent — or I can go to this concert, it's a no-brainer," she said. "But it didn't used to be that way."

Elfassy represents a growing cohort of consumers who aren't willing to keep up with the rising prices for live music, creating a K-shaped demand curve where higher-income consumers are spending more — and keeping prices inflated — while lower-income consumers are pulling back.

That dynamic has played out across discretionary spending categories, like retail, dining and travel, as Americans grapple with persistent inflation, economic uncertainty and, now, soaring gas prices.

In live music, this K-shaped environment is spurring fears that the lower end of the market is falling out entirely.

Some are calling the demand shifts "blue dot fever," named for the blue dots on Ticketmaster seating maps that denote an unsold ticket. For some artists, it's forcing them to take a critical look at their performances. Post Malone, Zayn and The Pussycat Dolls are just a few examples of artists who have canceled shows or tours in recent months, with the last group openly admitting that poor ticket sales was the catalyst.

Last summer, even before the most recent pricing pressures, industry research suggested higher ticket prices were helping to prop up the overall health of the market. Goldman Sachs analysts wrote in a 2025 report that demand for live music was expected to grow at a 7.2% compounded annual growth rate between 2024 and 2030.

Average ticket price for a concert in one of the top 100 global tours, the report found, was $136 in 2024, up 50% from an average of $91 in 2019.

How inflation is changing concert spendingSeveral of the major ticketing companies told CNBC they're not seeing more show cancellations this summer than an average year.

"Of all the shows Live Nation has on the books this year, less than 1% have been cancelled," a spokesperson for the Ticketmaster parent said. "That's not 'blue dot fever' — it's a normal touring year; in fact, 2026 is shaping up to be a record with concert ticket sales up 11% for the year."

The spokesperson added that roughly 70% of tickets sold on its platform are priced under $100.

Live Nation and Ticketmaster have faced scrutiny over the company's ticketing practices and dominant influence in the music industry. The company faced legal challenges over alleged anticompetitive behavior and reached a settlement with the Department of Justice in March. A federal jury found last month that Live Nation held an anticompetitive monopoly, though the company said in a statement at the time, "The jury's verdict is not the last word on this matter."

StubHub, a ticket reseller, told CNBC that the company is seeing the K-shaped pattern take shape in live music, with demand diverging fast between various events.

While StubHub said overall concert demand is up nearly 10% year-over-year, it's not across the board. Ticket demand for stadium-scale events is up significantly, while demand for mid-size and smaller venues is waning.

The events that are struggling to sell are facing a "supply-sizing problem," according to Jill Gonzalez, head of consumer communications at StubHub. The events earning the strongest fan attention, she said, are stadium tours, residencies and marquee festivals.

"What our data makes clear is that fan demand for live music hasn't softened, but it's sharpened," Gonzalez told CNBC. "Fans are making deliberate choices about where they spend, and when they decide a show is worth it, the demand signal is as strong as anything we've seen on our platform."

Ticket platform SeatGeek said while more artists are announcing tours, the resale environment remains healthy.

"If you have more artists that are flooding the market with tours, you're going to have the gross number of cancellations pick up year-over-year, so that's expected," said Oliver Marvin, the company's senior director of strategic finance. "But the overall number, cancellations as a percentage of people who are out on tour, is not too much different than what we've seen in prior years."

He added that the company is seeing some consumers dive in for last-minute tickets out of hope the prices will drop for tours that aren't garnering as much immediate demand.

Why stadium tours still draw big demandExperts say dropping demand for some shows may be more nuanced than what meets the eye.

As prices everywhere rise, and consumers begin to be more intentional about how they're spending their money, the blame of unsold tickets may be more appropriately placed on the macroeconomic environment rather than on the artists themselves, according to Sam Howard-Spink, the director of music business at New York University.

"It's really mostly to do with the economics of live performance and touring right now, which is also at the moment, I would say, very closely tied to economic conditions and cost-of-living questions," Howard-Spink said.

Tighter spending among fans can turn a tour misstep into a disaster, he suggested, like if an artist plans dates at an inappropriately sizes venue or in an off-base market. While nostalgia for older acts can occasionally draw crowds, it's struggling to outweigh all other factors.

And while bigger artists can still sell out a stadium, less-popular acts are falling short.

"Harry Styles, Bad Bunny, Lady Gaga, Ariana Grande — these are acts of, 'I'm not really going to have too much trouble,'" he said. "But if you're talking about like ... an early 2000s band that might not just be able to pull in those crowds, maybe they are overconfident in the kinds of venues that they think that they can fill up."

Howard-Spink added that the business of music has long been considered largely "recession-resistant," even weathering the pandemic well. But because concert tickets are a scarce resource, as opposed to music streaming, it's allowed the prices to rise rapidly.

Music publicist Eric Alper noted artists couldn't have foreseen these macroeconomic factors currently at play when booking out their tours months in advance. There's also more artists on tour this year than past years, he said, crowding the schedule.

With prices broadly higher, fans are also seeking out more experiences that give them a bang for their buck, he added, as the live music scene sees a rise in residencies, along with unique new venues like The Sphere in Las Vegas.

"What people want, they want the choreography, they want the lights, they want the superior sound, they want great sightlines," Alper said. "They're not just going to sit there and spend $150 to go watch a band play with very bare bones."

Still, Alper said, he believes the diehard fans are willing to pay up.

"If you're a fan of an artist, I don't think you care about the high ticket prices as much as people think that they do," Alper said. "People want the experience, and they also want to tell people that they were there."
2026-06-12 15:50 2mo ago
2026-05-26 08:23 3mo ago
Why the Warner Bros. Discovery Merger Is Suddenly Facing New Pressure
LYV Live Nation Entertainment
FMP Stock News
Original source text
Warner Bros. Discovery (WBD) shares slipped on Friday after a report said Paramount Skydance (PSKY) hired a prominent lawyer to help defend its planned takeover
2026-06-12 15:50 2mo ago
2026-06-04 12:36 3mo ago
Live Nation (LYV) Down 2.1% Since Last Earnings Report: Can It Rebound?
LYV Live Nation Entertainment
FMP Stock News
Original source text
Live Nation (LYV) reported earnings 30 days ago. What's next for the stock?
2026-06-12 15:50 2mo ago
2026-06-05 15:40 3mo ago
Did Live Nation Entertainment, Inc. Insiders Breach their Fiduciary Duties to Shareholders?
LYV Live Nation Entertainment
FMP Stock News
Original source text
Shareholders are encouraged to contact the firm to discuss their rights and options at no cost or obligation. We would handle any matter on a contingent fee basis, whereby you would not be responsible for out-of-pocket payment of our legal fees or expenses.

Shareholders should contact the firm immediately as there may be limited time to enforce your rights. 

, /PRNewswire/ -- Halper Sadeh LLC, an investor rights law firm, is investigating whether certain officers and directors of Live Nation Entertainment, Inc. (NYSE: LYV) breached their fiduciary duties to shareholders.

If you currently own Live Nation stock and are a long-term shareholder, you may be able to seek corporate governance reforms, the return of funds back to the company, a court-approved financial incentive award, or other relief and benefits. Please click here to learn more about your legal rights and options or contact Daniel Sadeh or Zachary Halper at (212) 763-0060 or [email protected] or [email protected].

Why Your Participation Matters:

Shareholder involvement can help improve a company's policies, practices, and oversight mechanisms to create a more transparent, accountable, and effectively managed organization, which can enhance shareholder value.

Halper Sadeh LLC represents investors all over the world who have fallen victim to securities fraud and corporate misconduct. Our attorneys have been instrumental in implementing corporate reforms and recovering millions of dollars on behalf of defrauded investors.

Attorney Advertising. Prior results do not guarantee a similar outcome.

Contact Information:
Halper Sadeh LLC
One World Trade Center
85th Floor
New York, NY 10007
Daniel Sadeh, Esq.
Zachary Halper, Esq.
(212) 763-0060
[email protected]
[email protected]
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SOURCE Halper Sadeh LLP
2026-06-12 15:50 2mo ago
2026-06-08 18:29 3mo ago
New York Knicks Could Win First NBA Title In 53 Years: What That Means For Live Nation Stock
LYV Live Nation Entertainment
FMP Stock News
Original source text
For the first time since 1999, the New York Knicks have a home NBA Finals game at the iconic Madison Square Garden arena.

The team is up 2-0 on the San Antonio Spurs, two wins away from claiming its first NBA championship in 53 years, an event that could happen before the public company that owns the team is split up.

• Madison Square Garden stock is showing positive momentum. What should traders watch with MSGE?

New York Knicks Tickets in Hot Demand  The Knicks are in one of the largest TV markets and population areas for a professional sports team, making its championship run a huge revenue booster for several parties. Fans are paying up for tickets, with prices rivaling those of some Super Bowls.

Madison Square Garden Entertainment (NYSE:MSGE) owns the iconic namesake arena and is benefiting from home playoff games this season.

Madison Square Garden Sports (NYSE:MSGS) owns the New York Knicks, NHL's New York Rangers and other sports assets.

The Knicks have made the playoffs five of the past six seasons, including four straight postseasons. This marks the furthest the Knicks have made it in years, with an appearance in the NBA Finals. Last year, the team lost in the conference finals.

While the two Madison Square Garden public entities could win from the Knicks success in the playoffs, ticket companies are also benefiting from huge upfront demand for tickets and demand for resale tickets.

Ticketmaster helped the Knicks sell tickets for Game 3, set for Monday night, with hundreds of thousands of people joining a virtual line to pay thousands of dollars for tickets.

At the time of writing, the cheapest resale tickets were $4,850 on Ticketmaster and $5,197 on Stubhub.

Some Knicks fans made the trip to San Antonio for Game 1 or Game 2, where the cost to fly and buy a ticket was less expensive than what they will pay Monday for Game 3.

Live Nation could end up being one of the bigger winners from the Knicks’ postseason run, able to capture service fees and additional revenue on the tickets sold at face value by the team to the public, tickets sold to season ticket holders and the tickets sold on the resale market.

While Knicks fans could be rooting for a sweep and the team to win in four games in the best-of-seven series, investors in Live Nation or Madison Square Garden stocks may be hoping the series gets extended.

A sweep would mean only two home games in the finals, while going to Game 6 in New York would mean three home games in the finals.

The Knicks swept their opponents in the last two rounds, knocking out potential revenue by having fewer games. This year's postseason has included seven home games ahead of Monday's game. Last year, the Knicks had nine home playoff games without reaching the finals for comparison.

Madison Square Garden Sports to Get Boost TooSeaport Research Partners analyst David Joyce estimates the Knicks could get a $145 million revenue boost for its 2026 postseason success, as reported by FrontOfficeSports.

The analyst said the sweeps and fewer home games may have cost the team $29 million in missed revenue for the postseason, though.

Finals games are worth an estimated $20.3 million in revenue for the analyst, which means a sweep would be $40.6 million from the Finals, while having a third home game would mean $60.9 million in revenue.

That $145 million figure is extra revenue, as not reaching the postseason would have meant no revenue for the team over the last several weeks outside of low merchandise sales.

The analyst said the Knicks often raise their season ticket prices after making the playoffs, which could boost ticketing revenue next season. A championship could also make the team more popular and valued higher ahead of a potential spinoff by the parent company.

Analysts have been raising their price targets on Madison Square Garden Sports stock in recent weeks, potentially recognizing the extra revenue from the postseason run or seeing the boost in valuation the team could have ahead of next season.

Photo: Shutterstock

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© 2026 Benzinga.com. Benzinga does not provide investment advice. All rights reserved.

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2026-06-12 15:50 2mo ago
2026-06-11 08:00 3mo ago
Lowe's Introduces Exclusive Live Music Benefits and Experiences for Loyalty Members
LYV Live Nation Entertainment
FMP Stock News
Original source text
Across select amphitheaters nationwide, Lowe's is giving loyalty members exclusive perks and new ways to connect through live music all year long

, /PRNewswire/ -- Lowe's is bringing MyLowe's Rewards* and MyLowe's Pro Rewards* members exclusive live music experiences through a new multi-year partnership with Live Nation. Members can access exclusive concert perks throughout the season, including discounted kids tickets† with purchase of an adult lawn ticket, complimentary lawn chair rentals at select shows for the first fifty eligible members^ and sweepstakes for a chance to win free tickets all year long. Helping members get more from the experiences they value most, these exclusive offers unlock more ways to enjoy live music with friends and family.

Lowe’s is bringing MyLowe’s Rewards and MyLowe’s Pro Rewards members exclusive live music experiences through a new multi-year partnership with Live Nation. The partnership also makes Lowe's the first presenting partner of a new amphitheater tailgate experience Live Nation is introducing at select venues this summer. Creating a new way for fans to kick off their night out, the spaces will bring together live entertainment, food and beverage offerings and programming from select Lowe's vendor partners, with specific experiences tailored by venue at North Island Credit Union Amphitheatre, Ruoff Music Center and Jiffy Lube Live. Tailgates begin when general parking lots open, with space available on a first-come, first-served basis.

Through the partnership, Lowe's is meeting customers where they already love to spend time, creating new ways to connect through live music and shared experiences. Designed to deliver both everyday value and meaningful moments, rewards members also get additional ways to save and earn. The free MyLowe's Rewards and MyLowe's Pro Rewards programs, now with more than 30 million members combined, offer personalized savings, bonus points and access to exclusive products and seasonal perks.

Each year, millions of fans return to amphitheaters as part of their summer routines, with 80% saying their local live music venues play a role in the moments they look forward to most with family and friends.

"Music is one of the things that brings people together — families, friends and entire communities — and we love being part of the moments people look forward to all year long," said Jen Wilson, Lowe's senior vice president and chief marketing officer. "Through this partnership, we're leveraging live music to reach new and younger audiences while giving our existing members exclusive perks that make these experiences even more rewarding. It's all about helping families make the most of a night out and rewarding loyalty by showing up in meaningful ways beyond the home."

"When fans come out to a show, they want the whole night to feel special," said Russell Wallach, Global President, Media & Sponsorship at Live Nation. "Jen and the Lowe's team really understood that from the start. We saw an opportunity to build around the moments fans already love during the summer and create more ways for people to spend time together before the music even starts through our new tailgate spaces presented by Lowe's."

MyLowe's Rewards and MyLowe's Pro Rewards members can access these benefits starting this summer at participating amphitheaters, with additional perks to come throughout the year. Learn more at https://www.lowes.com/concertperks.

*Loyalty Programs subject to Terms & Conditions. See Lowes.com/Terms for full program details. Subject to change. MyLowe's Rewards Program subject to terms & conditions. Visit Lowes.com/Terms for details. Subject to change.   
†MyLowe's Rewards members who receive a unique code via MyLowe's Rewards communications may purchase "2 for 1" lawn tickets (1 adult ticket and 1 child ticket) to participating concerts, while supplies last. For each participating concert, the first fifty (50) Members 18 years of age or older who enter their code at ticket check out will be able to purchase two (2) discounted tickets. Must purchase two (2) tickets and enter an eligible code to receive the offer. Ticket prices are "all in" pricing. The child using a ticket must be 12 years of age or younger and accompanied at all times at the concert by a parent or legal guardian. Offer is limited to one (1) per customer. Any customer found violating the terms of the Offer may be disqualified. Offer cannot be combined with other offers or discounts, cannot be used on past purchases, and is void where prohibited.
^The first fifty (50) MyLowe's Rewards members ("Members") at each participating concert who go to the chair rental location and show their Member ID in the Lowe's app will receive a complimentary chair rental, while supplies last. Members must be 18 years of age or older. Must have a valid concert ticket to claim offer. Offer is limited to one (1) complimentary chair per Member per concert. Offer has no cash value and is void where prohibited. Check venue policy for chair usage terms and return instructions. Sponsor may cancel or suspend the Offer at any time without notice or liability. Sponsor: Lowe's Companies, Inc. 

About Live Nation Entertainment
Live Nation Entertainment (NYSE: LYV) is the world's leading live entertainment company comprised of global market leaders: Ticketmaster, Live Nation Concerts, and Live Nation Sponsorship. For additional information, visit www.livenationentertainment.com.

About Lowe's
Lowe's Companies, Inc. (NYSE: LOW) is a FORTUNE® 100 home improvement company with total fiscal year 2025 sales of more than $86 billion. Lowe's employs approximately 300,000 associates and operates over 1,750 home improvement stores, 540 branches and 120 distribution centers. Based in Mooresville, N.C., Lowe's supports the communities it serves through programs focused on creating safe, affordable housing, improving community spaces, helping to develop the next generation of skilled trade experts and providing disaster relief to communities in need. For more information, visit Lowes.com.

Contact:
Lowe's Media Team
Amanda Caskey
[email protected]

Live Nation Media Team
Danika Azzarelli
[email protected]

SOURCE Lowe's Companies, Inc.
2026-06-12 15:50 2mo ago
2026-06-12 07:26 2mo ago
American Express, Live Nation And A Health Care Stock: CNBC's 'Final Trades'
LYV Live Nation Entertainment
FMP Stock News
Original source text
On the earnings front, American Express reported upbeat first-quarter 2026 results on April 23. The company reported quarterly revenue (net of interest expense) growth of 10% year-over-year to $18.91 billion, topping the analyst consensus estimate of $18.62 billion.

Higher Card Member spending drove the increase, along with higher net interest income, growth in card balances and strong card fee growth.

Don't forget to check out our premarket coverage here

Rob Sechan, CEO of NewEdge Wealth, named Eli Lilly and Company (NYSE:LLY) as his final trade.

According to recent news, Eli Lilly announced on June 9 that the U.S. Food and Drug Administration has approved the company's EBGLYSS (lebrikizumab-lbkz) for one maintenance dose every eight weeks in patients with moderate-to-severe atopic dermatitis.

Joshua Brown, co-founder and CEO of Ritholtz Wealth Management, said Live Nation Entertainment, Inc. (NYSE:LYV) is on the verge of a new 52-week high.

Morgan Stanley analyst Cameron Mansson-Perrone, on Wednesday, maintained Live Nation Entertainment with an Overweight rating and raised the price target from $185 to $200.

Price Action Eli Lilly shares gained 2.2% to close at $1,160.95 on Thursday. American Express shares rose 1.6% to settle at $318.49 during the session. Live Nation shares climbed 2.9% to close at $172.33 on Thursday. Photo via Shutterstock

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2026-06-12 15:50 2mo ago
2026-03-23 09:00 5mo ago
China SXT Pharmaceuticals, Inc. Announces Share Re-classification
SXT Sensient Technologies
FMP Stock News
Original source text
TAIZHOU, China, March 23, 2026 (GLOBE NEWSWIRE) -- China SXT Pharmaceutics, Inc. (Nasdaq: SXTC) (the “Company” or “SXTC”),  a specialty pharmaceutical company focusing on the research, development, manufacturing, marketing, and sales of Traditional Chinese Medicine Pieces (“TCMPs”), including Advanced TCMPs (Directly-Oral TCMP and After-Soaking-Oral TCMP), fine TCMPs, regular TCMPs, and TCM Homologous Supplements (“TCMHS”), today announced that upon the market opening on March 24, 2026, the Company’s Class A Ordinary Shares will be traded on The Nasdaq Stock Market under the symbol “SXTC”.

On July 28, 2025, the Company held a special meeting of shareholders (the “Meeting”). At the Meeting, shareholders approved a change to the Company’s authorized share capital to establish a dual class share structure by (i) creating a new class of shares consisting of unlimited Class B Ordinary Shares, which entitle the holder to fifty (50) votes per Class B Ordinary Share on any resolution of shareholders, and (ii) designating the Company’s existing Ordinary Shares as Class A Ordinary Shares, each with no par value (the “Share Re-classification”). The Share Re-classification became effective upon filing of the Amended and Restated Memorandum and Articles of Association with the Companies Registry of the British Virgin Islands by the Company. The Company is authorized to issue an unlimited number of shares, divided into two Classes consisting of Class A Ordinary Shares with no par value and Class B Ordinary Shares with no par value.

Upon the effectuation of the Share Re-classification, shareholders holding shares through a bank, broker or other nominee will have their shares automatically adjusted to reflect the Share Re-classification.  Beneficial holders may contact their bank, broker or nominee for more information. Please direct any questions to your broker or the Company's transfer agent, Transhare Corporation, by calling +1 303-662-1122.

About China SXT Pharmaceuticals, Inc.

Founded in 2005 and headquartered in Taizhou City, Jiangsu Province, China, China SXT Pharmaceuticals, Inc. is an innovative pharmaceutical company focusing on the research, development, manufacture, marketing and sales of traditional Chinese medicine pieces, which is a type of Traditional Chinese Medicine that has been processed to be ready for use. For more information, please visit www.sxtchina.com.

Safe Harbor Statement

This press release contains forward-looking statements. Forward-looking statements include statements concerning plans, objectives, goals, strategies, future events or performance, and underlying assumptions and other statements that are other than statements of historical facts. The Company’s actual results may differ materially from those expressed in any forward-looking statements as a result of various factors and uncertainties. The reports filed by the Company with the Securities and Exchange Commission discuss these and other important factors and risks that may affect the Company’s business, results of operations and financial conditions. For these reasons, among others, investors are cautioned not to place undue reliance upon any forward-looking statements in this press release. The Company undertakes no obligation to publicly revise these forward-looking statements to reflect events or circumstances that arise after the date hereof.

For more information, please contact:

Feng Zhou, Chief Executive Officer

Email: [email protected]
2026-06-12 15:50 2mo ago
2026-03-24 13:39 5mo ago
Congress Asset Management Co. Has $69.01 Million Stake in Sensient Technologies Corporation $SXT
SXT Sensient Technologies
FMP Stock News
Original source text
Congress Asset Management Co. grew its position in Sensient Technologies Corporation (NYSE: SXT) by 2.5% during the fourth quarter, according to the company in its most recent disclosure with the Securities and Exchange Commission (SEC). The institutional investor owned 734,573 shares of the specialty chemicals company's stock after purchasing an additional 17,935 shares
2026-06-12 15:49 2mo ago
2026-03-26 08:00 5mo ago
Sensient Scales Up Natural Color Production to Fuel U.S. Shift from Synthetic Dyes
SXT Sensient Technologies
FMP Stock News
Original source text
Unprecedented demand for natural colors spurs significant capital investment in Sensient's Natural Color Manufacturing Capacity, including expansion of largest production site in St. Louis, Missouri

, /PRNewswire/ -- On March 23rd, Sensient Food Colors, a division of Sensient Technologies (NYSE: SXT), officially celebrated the commencement of a major expansion at its largest natural color plant, which is located in St. Louis, Missouri. The expansion, coined Project Prism, is one of the many capital investments planned by Sensient to support the food and beverage industry's rapid transition away from artificial colors in the United States. Sensient expects to spend up to $250 million in the coming years to expand its natural color manufacturing capacity, supply chain, and personnel.

Sensient Project Prism Groundbreaking Event, March 2026

Sensient Project Prism Groundbreaking Event, March 2026

Sensient Project Prism Groundbreaking Event, March 2026

Sensient Project Prism Groundbreaking Event, March 2026

Sensient Project Prism Groundbreaking Event, March 2026

Sensient Project Prism Groundbreaking Event, March 2026

Sensient Project Prism Groundbreaking Event, March 2026

The St. Louis natural colors plant expansion is being done in partnership with Burns & McDonnell and will add 28,800 square feet of specialized processing and production capacity onto Sensient's existing 500,000 square foot manufacturing facility.

"Sensient has taken a defining role in accelerating the industry's transition to natural color solutions. We are reinforcing our leadership position by making significant investments in capacity and infrastructure to facilitate the natural color conversion in the United States. The groundbreaking ceremony marks a pivotal milestone in our mission to better serve customers and lead this industry-wide change," stated Sensient Colors President, Steve Morris.

The groundbreaking ceremony was attended by distinguished guests, including Missouri Lieutenant Governor David Wasinger, and the President and CEO of the Regional Business Council of St. Louis, Karen Branding, and received coverage from local media outlets.

Sensient's St. Louis plant expansion is a testament to the company's service-first model and commitment to customer satisfaction and natural color innovation.

About Sensient Colors LLC

Sensient Colors brings life to products, adding color and visual enjoyment to food and beverage applications worldwide. Offering unparalleled color innovation and proprietary technologies, Sensient Food Colors applies industry defining color expertise, enhancing brand value through premium sensory appeal and performance. Sensient Colors LLC is headquartered in St. Louis, Missouri.

About Sensient Technologies

Sensient Technologies Corporation is a leading global manufacturer and marketer of colors, flavors, and other specialty ingredients. Sensient uses advanced technologies and robust global supply chain capabilities to develop specialized solutions for food and beverages, as well as products that serve the pharmaceutical, nutraceutical, and personal care industries. Sensient's customers range in size from small entrepreneurial businesses to major international manufacturers representing some of the world's best-known brands. Sensient is headquartered in Milwaukee, Wisconsin. www.sensient.com

Media Contact Information: 

Brittany V. Jones
Sensient Food Colors
Director of Marketing
[email protected]
+1 (557) 213-7278

SOURCE Sensient Food Colors
2026-06-12 15:49 2mo ago
2026-03-30 05:13 5mo ago
JPMorgan Chase & Co. Purchases 31,777 Shares of Sensient Technologies Corporation $SXT
SXT Sensient Technologies
FMP Stock News
Original source text
Posted by Defense World Staff on Mar 30th, 2026

JPMorgan Chase & Co. increased its position in shares of Sensient Technologies Corporation (NYSE:SXT – Free Report) by 47.5% in the third quarter, according to its most recent 13F filing with the Securities & Exchange Commission. The institutional investor owned 98,683 shares of the specialty chemicals company’s stock after purchasing an additional 31,777 shares during the quarter. JPMorgan Chase & Co. owned approximately 0.23% of Sensient Technologies worth $9,261,000 at the end of the most recent quarter.

Several other institutional investors have also recently added to or reduced their stakes in SXT. Eminence Capital LP acquired a new stake in shares of Sensient Technologies during the second quarter worth approximately $99,117,000. Westwood Holdings Group Inc. bought a new position in shares of Sensient Technologies in the second quarter valued at approximately $91,280,000. Congress Asset Management Co. boosted its holdings in shares of Sensient Technologies by 4.4% in the 3rd quarter. Congress Asset Management Co. now owns 716,638 shares of the specialty chemicals company’s stock worth $67,257,000 after acquiring an additional 29,901 shares in the last quarter. Norges Bank acquired a new position in shares of Sensient Technologies in the 2nd quarter worth approximately $50,728,000. Finally, Parsifal Capital Management LP bought a new stake in Sensient Technologies during the 3rd quarter worth approximately $46,784,000. 90.86% of the stock is owned by institutional investors.

Sensient Technologies Price Performance Shares of SXT stock opened at $86.83 on Monday. Sensient Technologies Corporation has a 1 year low of $67.79 and a 1 year high of $121.54. The company has a current ratio of 4.10, a quick ratio of 1.53 and a debt-to-equity ratio of 0.59. The firm’s 50 day moving average is $93.39 and its 200-day moving average is $94.75. The firm has a market capitalization of $3.69 billion, a price-to-earnings ratio of 27.48 and a beta of 0.55.

Sensient Technologies (NYSE:SXT – Get Free Report) last issued its quarterly earnings results on Friday, February 13th. The specialty chemicals company reported $0.72 earnings per share for the quarter, missing analysts’ consensus estimates of $0.78 by ($0.06). Sensient Technologies had a net margin of 8.34% and a return on equity of 12.82%. The company had revenue of $393.45 million during the quarter, compared to analyst estimates of $395.70 million. During the same period in the prior year, the business earned $0.70 EPS. The business’s revenue for the quarter was up 4.5% on a year-over-year basis. Sensient Technologies has set its FY 2026 guidance at 3.600-3.800 EPS. Sell-side analysts forecast that Sensient Technologies Corporation will post 3.1 EPS for the current fiscal year.

Sensient Technologies Announces Dividend The company also recently announced a quarterly dividend, which was paid on Monday, March 2nd. Stockholders of record on Tuesday, February 3rd were given a dividend of $0.41 per share. The ex-dividend date was Tuesday, February 3rd. This represents a $1.64 dividend on an annualized basis and a dividend yield of 1.9%. Sensient Technologies’s payout ratio is presently 51.90%.

Analyst Ratings Changes Several brokerages have issued reports on SXT. Weiss Ratings reiterated a “hold (c+)” rating on shares of Sensient Technologies in a research report on Monday, December 29th. Zacks Research cut Sensient Technologies from a “hold” rating to a “strong sell” rating in a report on Tuesday, February 17th. One equities research analyst has rated the stock with a Buy rating, two have issued a Hold rating and one has assigned a Sell rating to the company. According to MarketBeat, Sensient Technologies currently has a consensus rating of “Hold” and an average target price of $110.00.

Check Out Our Latest Analysis on SXT

Sensient Technologies Profile (Free Report)

Sensient Technologies Corporation is a global leader in the manufacture and supply of colors, flavors and fragrances for a broad range of end-markets. The company develops and produces ingredients that enhance the appearance, taste and scent of products in the food, beverage, nutraceutical, pharmaceutical, personal care and household sectors. Its portfolio includes natural and synthetic colorants, botanical and artificial flavor systems, fragrance compounds and specialty chemical offerings tailored to customer specifications.

Within its flavor and fragrance division, Sensient provides custom formulations for sweet, savory and umami taste profiles along with fragrance blends for personal care and cosmetic applications.

Further Reading Five stocks we like better than Sensient Technologies Want to see what other hedge funds are holding SXT? Visit HoldingsChannel.com to get the latest 13F filings and insider trades for Sensient Technologies Corporation (NYSE:SXT – Free Report).

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