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2025-11-25 13:54 5mo ago
2025-11-25 08:16 5mo ago
VanEck quietly backpedals on BNB ETF staking in latest SEC filing cryptonews
BNB
Asset manager VanEck backed away from its earlier plans to stake assets in its proposed spot BNB exchange-traded fund, despite offering staking in its recently launched Solana product.

In its updated S-1 filing to the US Securities and Exchange Commission (SEC) on Friday, VanEck said “the Trust will not employ its BNB in Staking Activities and accordingly will not earn any form of staking rewards or income of any kind from Staking Activities” at the time of listing. The filing further warns that “there can be no assurance that the Trust will engage in any Staking Activities” in the future, either.

The company acknowledged that avoiding staking could cause the ETF’s performance to lag that of holding BNB (BNB) directly, noting that investors would forgo potential staking rewards.

This follows VanEck filing for a spot BNB exchange-traded fund (ETF) in May. The filing noted at the time that it “may, from time to time, stake a portion of the assets through one or more trusted staking providers.” Earlier this month, VanEck also launched the US’s third Solana (SOL) ETF, offering staking yields.

VanEck’s BNB ETF S1 filing. Source: SECVanEck hints at BNB’s regulatory woesIn its updated filing, VanEck distanced itself from any potential staking efforts and stated that it would be implemented through one or more third-party “Staking Services Providers.” Furthermore, the company clearly stated that there was no guarantee that any staking with ETF assets would ever take place, and if they were to engage in such activity, they would first file a prospectus with the SEC.

“The Trust is not permitted to engage in Staking Activities, which could negatively affect the value of the Shares.”Still, the filing fails to clearly state the rationale for its cautious approach to BNB staking, but it hints at concerns regarding regulatory troubles. A section of the filing clearly states that a determination by the SEC that BNB is a security may adversely affect the value of the shares and the termination of the trust.

“The test for determining whether a particular digital asset is a ‘security’ is complex and difficult to apply, and the outcome is difficult to predict,” VanEck said. The fund manager “acknowledges that BNB may currently be a security, based on the facts as they exist today, or may in the future be found by the SEC or a federal court to be a security.”

In such a case, VanEck may dissolve the ETF — either of its own volition by autonomously determining that BNB is a security or after the SEC or a federal court concludes that it is. “For so long as the Sponsor believes there to be good faith grounds to conclude that the Trust’s BNB is not a security, the Sponsor does not intend to dissolve the Trust on the basis that BNB could at some future point be determined to be a security,” the filing said.

BNB’s past brushes with the SECAs VanEck pointed out, in 2023, the SEC filed lawsuits against crypto exchange Binance, its US-based competitor, Coinbase, and Kraken for facilitating the trading of unregistered securities. The regulator deemed 68 digital assets to be securities at the time, including BNB. Still, in early July last year, a US federal court found that secondary sales of the BNB token did not constitute security transactions.

Whether staking and cryptocurrencies that employ it fall under securities law has been subject to intense debate. Back in late May, the SEC’s Division of Corporation Finance said in a statement that “Protocol Staking Activities” such as crypto staked in a proof-of-stake blockchain, “don’t need to register with the Commission transactions under the Securities Act,” or fall within “one of the Securities Act’s exemptions from registration.”

Still, this did not settle the debate. At the time, Caroline Crenshaw was the sole commissioner who opposed the guidance, saying it “fails to deliver a reliable roadmap for determining whether a staking service” is an investment contract under securities laws.

Magazine: Ethereum’s Fusaka fork explained for dummies: What the hell is PeerDAS?
2025-11-25 13:54 5mo ago
2025-11-25 08:18 5mo ago
Metaplanet Secures $130M Loan to Expand Bitcoin Holdings cryptonews
BTC
Key NotesAsian MicroStrategy, Metaplanet, has secured $130 million loan for the acquisition of more Bitcoin.This follows an initial $100 million loan, which was also directed to BTC purchase.These loans were secured by the Bitcoin already held by the company.
Asian financial firm Metaplanet has secured $130 million in loans to acquire more Bitcoin

BTC
$87 051

24h volatility:
0.9%

Market cap:
$1.74 T

Vol. 24h:
$71.37 B

.

This move reflects its commitment to boosting its BTC holdings and establishing the company’s position in the broader crypto industry.

The secured credit facility has a total limit of $500 million, and $230 million have already been drawn.

Metaplanet Reaffirms Strong Bitcoin Position
On November 21, Metaplanet executed a new loan, worth $130 million, under its credit facility. This facility has a total limit of $500 million, with $230 million already drawn.

The loan was secured by the BTC held by the company, and the identity of the lender was not disclosed in the published document. The loan features daily automatic renewal.

The loan can be repaid at any time, at the discretion of Metaplanet with no fixed maturity date.

The company plans to direct a portion of this capital to the acquisition of more Bitcoin. In addition, it would expand Bitcoin-based revenue operations and repurchase shares when market conditions allow.

Metaplanet already holds 30,823 BTC, worth $3.1 billion as of Nov. 19, and is sufficient to cover collateral requirements.

This is just one of the numerous times that Metaplanet has secured a loan to pursue a large BTC acquisition. On Nov. 5, it executed a $100 million loan secured by its Bitcoin holdings.

The loan was finalized on Oct. 31 under a credit facility agreement established Oct. 28. Like in the case of the recent loan, the lender was not disclosed at the request of the counterparty.

Metaplanet Commits $119 Million to BTC Purchase
Only a few days ago, Metaplanet committed $119 million out of its $151 million preferred share raise to boost its Bitcoin-related operations.

This represents 73% of the total proceeds. The fund is meant for purchases scheduled between December 2025 and March 2026.

Of the total, $107 million will be used to buy Bitcoin, while the remaining $12 million is set aside for options trading.

Looking ahead, Metaplanet aims to hold one of the largest Bitcoin positions in the industry, likely competing with Strategy, which currently holds 649,870 BTC.

Disclaimer: Coinspeaker is committed to providing unbiased and transparent reporting. This article aims to deliver accurate and timely information but should not be taken as financial or investment advice. Since market conditions can change rapidly, we encourage you to verify information on your own and consult with a professional before making any decisions based on this content.

Cryptocurrency News, News

Benjamin Godfrey is a blockchain enthusiast and journalist who relishes writing about the real life applications of blockchain technology and innovations to drive general acceptance and worldwide integration of the emerging technology. His desire to educate people about cryptocurrencies inspires his contributions to renowned blockchain media and sites.

Godfrey Benjamin on X
2025-11-25 13:54 5mo ago
2025-11-25 08:19 5mo ago
XRP Price Holds Above Key Support as ETF Launch Generates $85.7M in First-Day Volume—What's Next? cryptonews
XRP
XRP’s long-awaited ETF debut has delivered a stronger-than-expected first push, with the four newly listed funds generating $85.7 million in opening-day trading volume. The inflows are already reshaping intraday price behavior—even as XRP price hovers in a tight technical range and tests a critical support zone.

Bitwise led convincingly with $36.6M, Franklin Templeton followed at $23.6M, Canary posted $18.7M, and Grayscale trailed at $6.7M, signaling an early demand imbalance that traders will be watching closely through the week.

XRP Price Analysis: Support Holds, but Breakout Requires a Key TriggerOn the charts, XRP continues to respect the micro-support band around $1.9, bouncing precisely from the 38.2% Fibonacci retracement at $2.22. This level remains the immediate demand zone, preventing deeper downside.

For the bullish structure to stay intact, XRP must continue printing higher lows above $2.27–$2.18. So far, price action remains constructive, but momentum is capped below the $2.69–$2.84 resistance, which is the key breakout trigger for a trend reversal.

A daily close above this range would shift the medium-term outlook decisively bullish and open the path toward higher Fibonacci targets.

XRP ETF Demand Strengthens as Volume Hits $85.7MIn the past 24 hours, XRP ETFs have generated $85.7 million in combined trading volume, marking one of the strongest openings for a newly listed crypto fund group. Bitwise led decisively with $36.6M, followed by Franklin Templeton at $23.6M, Canary at $18.7M, and Grayscale trailing at $6.7M. 

This early distribution highlights concentrated institutional confidence in Bitwise’s product. Intraday flow shows clear strength during U.S. ETF trading hours, suggesting these vehicles are increasingly shaping XRP’s liquidity profile. If demand holds through the week, ETF momentum could act as the catalyst for a broader breakout—especially if price moves closer to the key $2.69–$2.84 resistance zone.

ConclusionXRP is holding its ground at a crucial support zone while ETF-driven interest injects steady liquidity into the market. The first day’s $85.7M volume signals that institutional curiosity is stronger than sentiment suggests.

All eyes now turn to the $2.69–$2.84 resistance. A breakout above this zone would confirm a shift in the trend and potentially accelerate XRP toward a new medium-term rally.

Trust with CoinPedia:CoinPedia has been delivering accurate and timely cryptocurrency and blockchain updates since 2017. All content is created by our expert panel of analysts and journalists, following strict Editorial Guidelines based on E-E-A-T (Experience, Expertise, Authoritativeness, Trustworthiness). Every article is fact-checked against reputable sources to ensure accuracy, transparency, and reliability. Our review policy guarantees unbiased evaluations when recommending exchanges, platforms, or tools. We strive to provide timely updates about everything crypto & blockchain, right from startups to industry majors.

Investment Disclaimer:All opinions and insights shared represent the author's own views on current market conditions. Please do your own research before making investment decisions. Neither the writer nor the publication assumes responsibility for your financial choices.

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2025-11-25 13:54 5mo ago
2025-11-25 08:22 5mo ago
Stellar ($XLM) Price Prediction 2025 cryptonews
XLM
Stellar sits near $0.248 after a tough month that pushed the token into a familiar support region. The $0.22–$0.20 zone triggered three major surges in the past and those rallies measured 32%, 53%, and an explosive 138%. Traders now wonder if history plans a repeat as Stellar X-Ray enters the spotlight and draws fresh interest into the project’s long-term roadmap.

X-Ray in Protocol 25: Zero-Knowledge Arrives on StellarProtocol 25 marks a major step in Stellar’s infrastructure story. The upgrade introduces X-Ray, a cryptographic toolkit designed for configurable privacy. Developers gain new power to build compliance-aligned privacy apps through zero-knowledge proofs. The upgrade stays aligned with Stellar’s transparency rules while still creating room for advanced privacy design.

Two cryptographic pillars define X-Ray. The first is BN254, a pairing-friendly curve used across many ZK systems. This curve powers privacy pools, ZK Email, Starknet, and many SNARK-based projects. Before Protocol 25, developers faced friction. They rewrote applications or used expensive workarounds. With support for bn254_g1_add, bn254_g1_mul, and bn254_multi_pairing_check, Stellar removes those barriers and matches Ethereum’s well-known precompiles.

The second pillar is Poseidon and Poseidon2, two ZK-optimized hash systems. These primitives unlock faster proof generation and smooth off-chain and on-chain alignment. Anyone building commitment structures, Merkle trees, or advanced ZK circuits gains new performance. It raises a question: how fast will developers migrate projects to Stellar now that feature parity improves?

Protocol 25 arrives with a clear timeline:

Testnet vote: January 7, 2026

Mainnet vote: January 22, 2026

The message from the Stellar Development Foundation is clear. Zero-knowledge is no longer a distant roadmap concept. It starts now.

Wirex and Stellar Activate Visa Stablecoin SettlementStellar’s privacy evolution arrives as adoption grows. Wirex launched dual-stablecoin Visa settlement using USDC and EURC for more than seven million users. The integration covers 130 countries, removes bank intermediaries and pushes settlement closer to real time.

This shift improves settlement flow in several ways:

Lower fees

Faster processing

Full 24/7 availability

Clearer USD and EUR tracking on-chain

The feature uses Wirex Pay’s stablecoin engine and aligns with broader payment plans. Users do nothing. The rollout follows Visa’s regional rules and keeps the same card experience. Stellar wants stablecoin settlement to become a natural part of global spending, and this update brings it a step closer.

Technical Setup: XLM Fights to Hold the 0.22 SupportStellar tapped $0.5 in July 2025 before price collapsed into a long bearish stretch. The descending trendline guided the drop until XLM broke it and retested the $0.3 level. The rejection sent price toward $0.22, the zone that now acts as a key pivot.

Source: X

This area has held through recent volatility. If buyers control it, the chart sets up a move toward $0.31. A clean break of that resistance has the potential to send XLM back to this year’s highs. Traders watch two clear conditions:

Hold $0.22 - Rally toward $0.31 resistance 

Break $0.22 - Decline toward $0.168 previous lows

Here is the part many traders find interesting. $XLM just tapped the same $0.22–$0.20 zone that triggered 32%, 53%, and 138% rallies. Will the level hold this time?  If this region holds, the reaction could be powerful.

XLM Price Prediction Table (2025)Month (2025)MinimumAverageMaximumOctober 2025$0.22$0.26$0.31November 2025$0.23$0.28$0.34December 2025$0.24$0.30$0.38Stellar now balances between powerful fundamentals and a technical zone with history. Protocol 25 unlocks real ZK potential. Wirex delivers real payments adoption. If price respects support, and bulls gain their momentum, they may regain control sooner than expected.
2025-11-25 13:54 5mo ago
2025-11-25 08:23 5mo ago
Solana DAT backs ‘double disinflation' plan amid 30% token decline cryptonews
SOL
Solana Digital Asset Treasury (DAT) DeFi Development Corp. (DFDV) expressed its support for a sweeping proposal aimed at accelerating the network’s disinflation schedule. 

On Tuesday, DFDV became the first Solana treasury to publicly endorse Solana Improvement Document (SIMD)-0411, a proposal to double Solana's annual disinflation rate from 15% to 30%, thereby reducing projected future emissions by over 22 million SOL over the next six years. 

“This proposal may come as a surprise to some, but its timing makes sense,” DFDV wrote. “The ecosystem has grown increasingly vocal about Solana’s current inflation schedule and its impact on SOL’s price.” 

Solana Strategic Reserve data shows that DFDV holds nearly 2.2 million Solana (SOL), worth about $300 million at the time of writing. This makes the company the third-largest corporate holder of SOL tokens. 

While DFDV’s support adds institutional weight to the high-stakes discussion, other DATs, such as Forward Industries or Solana Company, haven’t weighed in on the topic. 

Source: Mert MumtazProposal seeks to accelerate Solana disinflationHelius Labs developers introduced SIMD-0411 on Saturday, marking one of the most significant monetary policy proposals for Solana since its launch. 

The draft recommends doubling Solana’s annual disinflation rate from 15% to 30%, which would bring the network to its long-standing 1.5% terminal inflation rate in just three years rather than six. 

Proposal seeks to speed up Solana disinflation. Source: GitHubAccording to the modeling shared in the proposal, the change would reduce projected emissions by about 22 million SOL tokens, equivalent to about $3 billion, over a six-year period. 

The developers said that the existing inflation curve no longer reflected the network’s maturity, pointing toward network revenue, user activity and decentralized finance (DeFi) throughput. 

By trimming the issuance, proponents said that the network could reduce structural sell pressure and align it more closely with what institutional investors expect from a modern crypto asset. 

Solana price slide puts pressure on DATsCoinGecko data shows that SOL fell from $197 on Oct. 26 to $136 at the time of writing, a 30% decline in the past month. The sharp downturn added urgency to the inflation debate, with some of the top corporate holders sitting on heavy losses. 

According to CoinGecko, Forward Industries, the largest corporate SOL holder, faces an unrealized loss of about $646.6 million, representing a 41% decline from its aggregate purchase price.

Upexi, the fifth-largest corporate holder, also sits in the red, with about $31 million in unrealized losses, marking a 10% decline from its entry prices. 

DFDV, which publicly endorsed the proposal, is still in profit. CoinGecko data showed that the company remained up by about $62 million, reflecting a 26.6% unrealized gain on its SOL purchases to date.

Magazine: Ethereum’s Fusaka fork explained for dummies: What the hell is PeerDAS?
2025-11-25 13:54 5mo ago
2025-11-25 08:23 5mo ago
Solana treasury backs ‘double disinflation' plan amid 30% price decline cryptonews
SOL
Solana Digital Asset Treasury (DAT) DeFi Development Corp. (DFDV) expressed its support for a sweeping proposal aimed at accelerating the network’s disinflation schedule. 

On Tuesday, DFDV became the first Solana treasury to publicly endorse Solana Improvement Document (SIMD)-0411, a proposal to double Solana's annual disinflation rate from 15% to 30%, thereby reducing projected future emissions by over 22 million SOL over the next six years. 

“This proposal may come as a surprise to some, but its timing makes sense,” DFDV wrote. “The ecosystem has grown increasingly vocal about Solana’s current inflation schedule and its impact on SOL’s price.” 

Solana Strategic Reserve data shows that DFDV holds nearly 2.2 million Solana (SOL), worth about $300 million at the time of writing. This makes the company the third-largest corporate holder of SOL tokens. 

While DFDV’s support adds institutional weight to the high-stakes discussion, other DATs, such as Forward Industries or Solana Company, haven’t weighed in on the topic. 

Source: Mert MumtazProposal seeks to accelerate Solana disinflationHelius Labs developers introduced SIMD-0411 on Saturday, marking one of the most significant monetary policy proposals for Solana since its launch. 

The draft recommends doubling Solana’s annual disinflation rate from 15% to 30%, which would bring the network to its long-standing 1.5% terminal inflation rate in just three years rather than six. 

Proposal seeks to speed up Solana disinflation. Source: GitHubAccording to the modeling shared in the proposal, the change would reduce projected emissions by about 22 million SOL tokens, equivalent to about $3 billion, over a six-year period. 

The developers said that the existing inflation curve no longer reflected the network’s maturity, pointing toward network revenue, user activity and decentralized finance (DeFi) throughput. 

By trimming the issuance, proponents said that the network could reduce structural sell pressure and align it more closely with what institutional investors expect from a modern crypto asset. 

Solana price slide puts pressure on DATsCoinGecko data shows that SOL fell from $197 on Oct. 26 to $136 at the time of writing, a 30% decline in the past month. The sharp downturn added urgency to the inflation debate, with some of the top corporate holders sitting on heavy losses. 

According to CoinGecko, Forward Industries, the largest corporate SOL holder, faces an unrealized loss of about $646.6 million, representing a 41% decline from its aggregate purchase price.

Upexi, the fifth-largest corporate holder, also sits in the red, with about $31 million in unrealized losses, marking a 10% decline from its entry prices. 

DFDV, which publicly endorsed the proposal, is still in profit. CoinGecko data showed that the company remained up by about $62 million, reflecting a 26.6% unrealized gain on its SOL purchases to date.

Magazine: Ethereum’s Fusaka fork explained for dummies: What the hell is PeerDAS?
2025-11-25 13:54 5mo ago
2025-11-25 08:27 5mo ago
XRP Rallies as Franklin Templeton and Grayscale Roll Out Spot ETFs cryptonews
XRP
XRP just had a monster day, jumping over 9% to $2.21 after Franklin Templeton and Grayscale both launched spot XRP ETFs on Monday.
2025-11-25 13:54 5mo ago
2025-11-25 08:29 5mo ago
Berachain Founder Disputes Refund Report, Labels It “Inaccurate and Incomplete” cryptonews
BERA
TL;DR

Recent reporting claims that Nova Digital holds a potential $25 million refund right tied to its Series B investment.
Berachain co-founder Smokey the Bera rejects the allegation, arguing that the report omits critical contractual details.
Meanwhile, the BERA token trades far below institutional entry prices, putting pressure on investors as the network works to regain momentum after a difficult market phase.

Berachain is facing scrutiny over its fundraising terms after published documents suggested that Nova Digital obtained a unique refund option linked to its Series B participation. Smokey the Bera strongly disputes the interpretation, insisting that the report misrepresents both the clause and Nova’s exposure to market risk. The controversy has attracted attention from traders, analysts, and regulatory observers who now monitor the chain’s financial agreements more closely.

Berachain Funding Debate and Transparency Claims
Smokey states that Nova Digital remains a major token holder and continues to support the project, even as it separates from Brevan Howard. He explains that the clause referenced in the report relates to regulatory compliance requirements, not price protection. According to Smokey, these mechanisms address eligibility issues around holding locked digital assets in certain institutional strategies, and do not shield investors from losses. 

He rejects the notion of unfair advantages and highlights his own market exposure, claiming he has taken seven-figure losses on secondary purchases of BERA, which he presents as proof of commitment. Smokey also emphasizes that Nova agreed to provide liquidity support for the network after launch, reinforcing that its role extends beyond speculative positioning. Supporters of Berachain argue that the project continues to attract institutional interest despite volatile market performance.

Dispute Over Refund Terms in the Series B Round
The original investigation alleges that other investors were not informed of Nova’s clause. Smokey counters that all participants signed the same documentation, denying that any exclusive benefits were granted. However, some backers cited in the report insist they were unaware of protections tied to Nova’s investment, extending the controversy over disclosures.

This dispute emerges while BERA trades significantly below its previous highs, affecting portfolios that entered the round at much higher valuations. Despite the downturn and a temporary network halt triggered by a protocol vulnerability, Berachain restored operations without user losses and has moved forward with initiatives to expand liquidity and strengthen the network.

Although disagreement persists regarding the alleged refund arrangement, Berachain maintains that it operates with commercial legitimacy and real market exposure from both leadership and institutional partners. 
2025-11-25 13:54 5mo ago
2025-11-25 08:30 5mo ago
Metaplanet sets up for new BTC purchases with $130M loan announcement cryptonews
BTC
Metaplanet announced another $130M loan, with the potential to acquire more BTC. The loan is backed by Metaplanet's treasury, and is part of a $500M facility, of which the company has borrowed $230M to date.
2025-11-25 13:54 5mo ago
2025-11-25 08:32 5mo ago
Morning Minute: Monad's $4B Debut cryptonews
MON
Morning Minute is a daily newsletter written by Tyler Warner. The analysis and opinions expressed are his own and do not necessarily reflect those of Decrypt. Subscribe to the Morning Minute on Substack.

GM!

Today’s top news:

Crypto majors rallied hard on Monday along with stocks; BTC at $87,400
White House launched Genesis Project as Manhattan Project for AI
Monad debuted its MON token + mainnet; MON at $3.9B fdv
Saylor’s Strategy did not announce any buys; BMNR passed 3% of ETH supply
MetaMask introduced equity perps trading on mobile
🚀 Monad Launches Its MainnetA new high-performance layer-1 just went live.

Is the market ready for it?

📌 What HappenedMonad officially launched its public mainnet on Monday, kicking off one of the most anticipated Layer 1 debuts of the year.

For those unfamiliar, the Monad chain is built around a simple pitch: Ethereum-style development with much higher performance.

The team aims for massive throughput, low-latency block times, and parallel execution, all wrapped inside a fully EVM-compatible environment so developers don’t need to learn anything new.

The ecosystem was ready at launch.

Early apps included gaming, wagering, Telegram-native tools, and DeFi-adjacent consumer products, giving users something to actually do on day one. And there was a virtual beer pong game allowing real wagering (shout out to Bro.fun).

From a trading perspective, day 1 was volatile.

MON dropped to $0.025 ($2.5B FDV) quickly on open, going as low as $0.023 as people raced to sell their airdrops (ranging from $1k+ to $6k+ for most who were eligible). Then it rebounded over 50% to $0.038 before falling back towards the $0.03 range, before rallying back to $0.039 overnight.

🗣️ What Are They Saying“Monad’s founding thesis is that decentralized systems have superpowers of resilience, trustlessness, and and resistance to central control. But they need to further scale.

The result is a unique network that’s starting to accomplish this!” - Keone, Monad co-founder

"Excited for Monad to go live because it's one of the few tech-first chain launches. The EVM has the best tooling and developer ecosystem, but has been hamstrung by poorly-performing node and consensus implementations. Very cool to see a grounds-up rewrite" - 0xFoobar on X

🧠 Why It MattersMonad enters an L1 market that is more competitive than ever.

Performance alone isn’t enough anymore.

Users (and investors) care about what they can do on the chain. What apps are there?

And Monad did launch with a decent list of curated apps for day one (easily discoverable in their portal landing page, similar to how Abstract launched).

The billion-dollar question, though, will users remain past day one?

Well, the team has $1B+ to incentivize teams to build apps to attract those users.

The Monad ecosystem development budget is 38.5% of the 100B token supply. That’s $1.15B at the time of writing. And the team will dangle those tokens as carrots for teams to come and build on Monad over the coming months and years.

That token allotment is a bit part of the longer-term Monad bull case. But it’s also a big part of the near-term bull case.

Very few of those tokens have been given out. So what tokens are out there in the wild?

Only the 3.3% from the airdrop and 7.5% from the ICO sale are substantially a part of the “float.” And every other token bucket has at least a 1-year lock on it. So MON will be a very low float (~12%) token for the foreseeable future.

But for the bull case to be realized, users still have to come and transact on Monad.

We will find out soon enough if they are able to pull that off…

🌎 Macro Crypto and MemesA few Crypto and Web3 headlines that caught my eye:

Crypto majors are very green tailing stocks on a very green day for markets; BTC +2% at $87,400; ETH +4% at $2,920, BNB +1% at $850, SOL +5% at $136
KAS (+22%), ENA (+13%), and SUI (+11%) led top movers
The NASDAQ jumped 2.7% yesterday as stocks like GOOG (+6%) and TSLA (+7%) soared
The White House launched the “Genesis Mission” as a Manhattan Project for AI
Binance and CZ are accused of enabling crypto transactions for Hamas in a new lawsuit
Kraken teased a debit card launch coming today
Tether bought another 1M Rumble shares, sending the YouTube rival’s stock sharply higher
The European Central Bank repeated warnings that rapidly growing stablecoins could pose “stability risks” to the broader financial system
In Corporate Treasuries / ETFs

Strategy (MSTR) skipped its latest weekly Bitcoin buy announcement for the first time in weeks (MSTR -67% from peak)
BitMine Immersion Technologies bought $195M of Ethereum, lifting its holdings to about 3% of supply (BMNR +10%)
Franklin Templeton launched its Franklin XRP ETF on NYSE Arca
Grayscale rolled out new DOGE and XRP ETFs on NYSE Arca
In Memes / Onchain Movers

Memecoin leaders are green led by Fartcoin again; DOGE +3%, Shiba +3%, PEPE +6%, PENGU +10%, BONK +9%, TRUMP +1%, SPX +8%, and FARTCOIN +23%
SPSC jumped 98% leading onchain movers; arc (+65%), 67 (+30%) and chillguy (+23%) were other notable movers
💰 Token, Airdrop & Protocol TrackerHere’s a rundown of major token, protocol and airdrop news from the day:

Monad debuted its mainnet and MON token, opening at $3.6B fdv after nearly a day of trading
MetaMask introduced new equity perps on mobile, allowing users to go long or short stocks like NVDA or TSLA
MegaUSD deposits go live today at 9 am ET, meant to seed USDm supply in the ecosystem (capped at $250M)
The Virtuals team promised refunds after a bad actor from the Basis OS team stole user funds in a security breach
🚚 What is happening in NFTs?Here is the list of other notable headlines from the day in NFTs:

NFT leaders were very green on Monday; Punks +3% at 31 ETH, Pudgy +7% at 5.7, BAYC +1% at 5.94 ETH; Hypurr’s +10% at 700 HYPE
Autoglyphs (+20%) were notable movers
Art Blocks announced its final 3 projects for AB 500, featuring the original 3 artists Snowfro, Daniel Calderon and Jeff Davis
Jack Butcher teased ‘Self Checkout’ as an IRL mint experience at Art Basel
Daily Debrief NewsletterStart every day with the top news stories right now, plus original features, a podcast, videos and more.
2025-11-25 13:54 5mo ago
2025-11-25 08:35 5mo ago
Bitcoin Decline Exposes FDV Forecast Flaws, Monad's Debut Underscores the Risk cryptonews
BTC MON
TL;DR:

Monad’s MON token launched with 10% of total supply, anchoring FDV at $3.2 billion amid Bitcoin’s drop.
Low-float structure caused misaligned trader expectations, illustrating FDV’s limitations in bearish markets.
Small price moves reflected headline valuations, not liquidity, emphasizing that scarcity and macro volatility can break FDV forecasts.

Monad launched its MON token on Monday with only a small fraction of the total supply in circulation, highlighting a key challenge in crypto valuation. With Bitcoin dropping from roughly $120,000 to below $85,000 in the weeks leading to the listing, the market environment was already bearish, making Monad’s debut a critical test of fully diluted valuation (FDV) metrics.

FDV forecasts break amid low-float launch
The MON token debuted with just over 10.8 billion tokens circulating, about 10% of the total 100 billion supply. This thin float anchored the FDV at $3.2 billion, regardless of actual market demand. Traders had previously speculated on an $8 billion outcome, but bearish sentiment paired with the limited float created a valuation that appeared inflated, demonstrating how FDV can become an optical illusion rather than a true signal of market appetite.

The launch exposed how low-float tokenomics distort trader expectations. Small price movements in such launches can produce headline valuations that seem massive, but the underlying liquidity remains shallow. Despite concerns about slow sales momentum, large team allocations, and potential airdrop selling, the structure maintained FDV above $3 billion unless the price sharply dropped. This misalignment illustrated that macro factors, like Bitcoin’s decline, were often overweighted in trader forecasts, while the token’s supply mechanics were underappreciated.

For short-term traders, Monad’s listing underscored that FDV forecasts can fail when scarcity and volatility collide. The listing did not reflect overwhelming demand but instead a valuation anchored by supply constraints. Long-term holders must also consider dilution risk from locked tokens, which will continue through 2026. The episode reinforces the importance of analyzing supply mechanics alongside market sentiment, particularly in launches with delayed unlocks and engineered scarcity.

Monad’s debut serves as a reference point for the limitations of FDV in low-float environments. When token distribution models favor small circulating supplies and slow unlock schedules, pricing frameworks can easily deviate from fundamentals. This event emphasizes that market mood often drives short-term pricing, while the math of supply plays catch-up later, highlighting the complex interplay between sentiment and tokenomics in crypto valuations.
2025-11-25 13:54 5mo ago
2025-11-25 08:39 5mo ago
Satoshi-Era Bitcoin Holder Rakes in 965,517,137% Profit After Recent Sell-Off cryptonews
BTC
Cover image via U.Today

Disclaimer: The opinions expressed by our writers are their own and do not represent the views of U.Today. The financial and market information provided on U.Today is intended for informational purposes only. U.Today is not liable for any financial losses incurred while trading cryptocurrencies. Conduct your own research by contacting financial experts before making any investment decisions. We believe that all content is accurate as of the date of publication, but certain offers mentioned may no longer be available.

A Satoshi-era Bitcoin (BTC) holder has cashed out 965,517,137% in profits following a recent sell-off. CryptoQuant analyst Maartunn spotlighted the news, describing it as a "wild on-chain story of the day."
 

Old Bitcoin trader cashes out from BTC salesMaartunn explained in an X post that a Bitcoin trader in the Satoshi era sold old coins that had not moved in years.

The wallet address originally held 13 BTC, and the owner has been systematically selling about 1 BTC per year since 2018.

Three days ago, the smart trader sold 1.02 BTC for roughly $84,000. These coins were mined in 2013 via Slush Pool, now Braiins, the very first mining pool ever created.

The realized price for those coins was $0.0087, less than one cent. Therefore, selling 1 BTC for about $84,000 means the trader gained more than 9.6 million times his initial investment. This translates to returns of 965,517,137%.

🧵 Wild on-chain story of the day

Long-Term Holder SOPR just flashed a massive spike: 80,472.

At a BTC price of ~$84K, that means someone just moved coins with a cost basis of about $1.00 each.

I dug into it… and found the transaction:
📅 22 Nov 2025 – 02:36:54
⛓️ Block… pic.twitter.com/OBW2gXlFFi

— Maartunn (@JA_Maartun) November 25, 2025 This trade is legendary on the market because the trader is an early miner who actually held and is now living the dream. They basically mined BTC when the difficulty was trivial, and electricity was the only cost.

The Satoshi-era holder never sold during the 2011, 2013, 2017 and 2021 bull runs. They also were not shaken out during bear markets.

Now, they are cashing out one single Bitcoin per year, and the remaining stack is still appreciating.

Institutions show less interest in BTCAlongside the BTC sell-off by the old miner, institutions like BlackRock have continued to move their holdings.

On Monday, Nov. 24, BlackRock deposited 2,822 BTC into Coinbase Prime. The move appeared as another of its repeated sales attempts, sparking discussions across the crypto community.

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Meanwhile, the latest sell-off attempt comes at a time when the market is showing signs of a potential rebound. The rapid price correction is slowing down as BTC recovered from the recent lows toward $87,500.

Despite the rebound, BlackRock is not willing to pause its selling streak. Just last week, the asset manager dumped more than $2 billion in Bitcoin and Ethereum.

Amid the market collapse, Strategy also failed to announce another BTC purchase. Famed short seller Jim Chanos has mocked Strategy Chairman Michael Saylor for this decision.

Chanos said Saylor did not buy Bitcoin following a major price correction, which appears to be counterintuitive.
2025-11-25 13:54 5mo ago
2025-11-25 08:39 5mo ago
Will CME's New Futures Impact the SOL Price Positively? Or Fall To $70 Coming? cryptonews
SOL
The SOL price is facing a decisive moment as it tests the upper boundary of its two-week horizontal range near $120. This level acts as the key pivot for bullish or bearish continuation.
2025-11-25 13:54 5mo ago
2025-11-25 08:44 5mo ago
Ripple Price Analysis: Has XRP Turned Bullish After Surge to Crucial Zone? cryptonews
XRP
Ripple’s XRP has printed its first meaningful relief bounce after a prolonged selloff, reclaiming the $2.10–$2.20 zone. Despite the short-term strength, the broader structure remains intact on the downside, and the reaction from the current resistance cluster will determine whether this move is merely a corrective retracement or the beginning of a deeper recovery.

XRP Price Analysis
By Shayan

The Daily Chart
The daily timeframe shows XRP rebounding firmly from the $1.90 demand block, a level that has acted as multi-month structural support. The move higher has now carried the price back into the multi-month flag pattern, indicating a bear trap.

This bounce is the first clean retest of the broken lower boundary of the flag. Historically, these retests often serve as decision points before continuation. Unless the asset can reclaim the $2.40–$2.50 region, the broader trend remains bearish, as this zone contains both a major order block and the region where multiple previous daily highs were swept before continuation to the downside.

RSI shows modest bullish momentum, rising from oversold conditions toward mid-range, but has not yet broken its multi-week ceiling. This suggests that while downward exhaustion is present, momentum is not yet strong enough to confirm a macro reversal.

A daily close above the $2.45 pivot would be the first indication of a structural shift. Failure to break through would keep downside targets open toward $1.80 and potentially the deeper demand zone around $1.60 should the broader market weaken again.

The 4-Hour Chart
The 4-hour timeframe highlights a sharp V-shaped rebound, driven initially by short-covering in the $1.95 region. The asset has now reached the confluence of the descending trendline and the red supply block at $2.30–$2.40, where early signs of exhaustion are visible.

RSI is hovering near 70, approaching intraday overbought levels while facing the most significant resistance of the past month. This increases the probability of a short-term pullback into the $2.15–$2.20 area, which has flipped into a temporary support level.

The main factor to watch is whether XRP can break and consolidate above the descending trendline. If this occurs, the next liquidity pockets sit around $2.55 and $2.75. Otherwise, rejection from here would raise the likelihood of another sweep of the $2.00 region before any larger recovery attempt.

Overall, the 4-hour market structure remains bearish until XRP closes decisively above the $2.40–$2.50 region.

Tags:
2025-11-25 13:54 5mo ago
2025-11-25 08:45 5mo ago
8% of Bitcoin changed hands in a week as markets on ‘knife's edge': Analysts cryptonews
BTC
8 minutes ago

Bitcoin saw one of its largest supply migrations ever as traders braced for the US Federal Reserve’s December rate decision and shifting expectations toward a rate cut.

90

A historic shift in Bitcoin ownership unfolded during the latest market downturn, while the broader crypto market remained tied to uncertainty over a possible US Federal Reserve rate cut in December.

Over 8% of the total Bitcoin (BTC) supply changed hands in the past seven days, making the current market decline “one of the most significant onchain events” in Bitcoin history, according to Joe Burnett, analyst and director of Bitcoin Strategy at Semler Scientific.

During previous significant Bitcoin supply movements, Bitcoin traded at about $5,000 in March 2020 and around $3,500 in December 2018, said Burnett in a Tuesday X post.

Both occasions marked a local bottom ahead of an accumulation phase that ultimately led to new all-time highs.

Still, up to half of the current Bitcoin supply movement may be attributed to a Coinbase Wallet Migration announced on Saturday, added Burnett.

Source: Joe BurnettBitcoin, crypto markets on “knife’s edge” ahead of Fed interest rate decision in DecemberMeanwhile, Bitcoin's price and investor sentiment remain on a “knife’s edge” due to mixed messages about December’s interest rate cut decisions, according to Nic Puckrin, digital asset analyst and co-founder of educational platform The Coin Bureau.

“What is more certain, though, is that the Fed holds the key to the market’s end-of-year finale, and its next rate decision will determine whether we get a Santa rally or a Santa dump,” he told Cointelegraph.

“As we get closer to Dec. 10, I expect market jitters to continue, and the Fed’s press conference will certainly have traders on the edge of their seats.”Interest rate cut expectations for the Federal Reserve’s Dec. 10 meeting have changed drastically during the past week

Interest rate cut probabilities. Source: CMEgroup.comMarkets are pricing in an 82% chance of a 25 basis point interest rate cut, up from 50% a week ago, according to the CME Group’s FedWatch tool.

The growing interest rate cut expectations were the main fuel leading to Bitcoin’s recovery from $81,000 to $87,000, according to Puckrin.

Magazine: Bitcoin is ‘funny internet money’ during a crisis: Tezos co-founder
2025-11-25 13:54 5mo ago
2025-11-25 08:47 5mo ago
None of Bitcoin's bull market peak indicators have been triggered yet, Coinglass cryptonews
BTC
Bitcoin has yet to flash a single confirmed market-top warning signal even after dwindling down 30.7% from its all-time high in early October, according to data from analytics platform Coinglass reviewed on Tuesday.
2025-11-25 13:54 5mo ago
2025-11-25 08:50 5mo ago
New York Times Square Turns “Ripple Square” as Franklin Templeton Elevates XRP to Icon Status cryptonews
XRP
Ripple Lights Up Times Square as Amonyx Declares the Dawn of the XRP EraTimes Square’s latest brand takeover has sent shockwaves through the crypto community. Market analyst Amonyx declared, “Times Square just turned into Ripple Square. When the billboards go blue, you know the XRP era has begun.” 

The remark comes as institutional interest in Ripple accelerates and market sentiment around XRP strengthens.

The towering blue-lit Ripple billboards electrifying Times Square couldn’t have arrived at a more pivotal moment. 

After years of regulatory battles, market volatility, and a resurgence of global interest in blockchain infrastructure, XRP’s takeover of one of the world’s most iconic advertising hubs signals far more than marketing hype. 

Therefore, it marks a clear narrative shift, Ripple is re-entering the spotlight with the confidence of a project gearing up for major, real-world adoption.

Notably, Amonyx’s remarks have intensified the buzz, framing the Times Square takeover as a clear signal of shifting market psychology. Analysts note that such high-profile visibility often foreshadows institutional moves, strategic partnerships, or major ecosystem updates. 

For XRP, the timing is pivotal, Ripple is rapidly scaling its global payments network while advancing real-world asset tokenization initiatives, making this moment more than just a marketing splash.

What next? Well, The Times Square display may not predict immediate price action, but it unmistakably elevates XRP’s cultural and institutional profile. 

This level of visibility signals Ripple’s push into the mainstream conversation, laying the groundwork for broader adoption, stronger market confidence, and a new phase of ecosystem momentum.

As Amonyx notes, when Times Square goes blue, it signals more than spectacle, it hints at a shift in momentum. Whether it marks the true beginning of the ‘XRP era’ is uncertain, but the message is unmistakable: Ripple is positioning for a major push, and the market is watching.

Franklin Templeton Declares XRP a “Foundational Building Block” in Digital PortfoliosGlobal asset manager Franklin Templeton is deepening its digital asset focus, highlighting XRP as pivotal to blockchain-driven investment strategies. 

Roger Bayston, Head of Digital Assets, noted that blockchain technology is transforming high-growth industries, with XRP at the forefront of this shift.

According to Bayston, 

“Blockchain innovation is driving fast-growing businesses, and digital asset tokens like XRP serve as powerful incentive mechanisms that help bootstrap decentralized networks and align stakeholder interests.” 

He further highlighted XRP’s role within sophisticated digital portfolios, stating that “within a diversified digital portfolio, we view XRP as a foundational building block.”

Franklin Templeton’s new XRP ETF, XRPZ, delivers institutional-grade exposure with regulated custody, full daily transparency, and deep liquidity, simplifying XRP investment while removing the complexities of direct on-chain management.

XRPZ marks a major step in bridging traditional finance and blockchain. By wrapping XRP into a regulated investment vehicle, Franklin Templeton opens access to investors drawn to XRP’s utility but wary of managing private keys, exchanges, or custody. The move also solidifies XRP’s standing as one of the few digital assets embraced through a long-term institutional lens.

Well, Franklin Templeton’s endorsement of XRP as a foundational digital portfolio asset highlights the rising view that select blockchain tokens can underpin next-generation financial systems. 

With a proven role in cross-border payments and expanding enterprise adoption, XRP is capturing the attention of asset managers navigating the convergence of decentralized and traditional finance.

With institutional adoption rising and regulated investment products expanding, Franklin Templeton’s XRPZ ETF could be a milestone for XRP’s mainstream legitimacy. For investors seeking transparent, regulated access to the digital economy, XRPZ provides a streamlined gateway to one of the most widely used blockchain assets.

ConclusionRipple’s takeover of Times Square is more than a visual spectacle, it signals XRP’s leap into a new era of visibility, confidence, and real-world relevance. 

As Amonyx notes, when one of the world’s busiest intersections turns Ripple blue, it reflects not just market excitement, but a decisive shift in narrative and momentum.

On the other hand, as digital assets reshape investing, Franklin Templeton’s endorsement of XRP as a foundational building block signals rising institutional confidence in blockchain. 

Through the XRPZ ETF, investors gain regulated, transparent, and liquid access to decentralized networks, reducing complexity and risk. This move underscores XRP’s growing role in the digital economy and highlights the potential of blockchain assets as key components of diversified, forward-looking portfolios.
2025-11-25 12:53 5mo ago
2025-11-25 07:30 5mo ago
Dragonfly Energy Broadens Product Lineup to Drive Growth Beyond Batteries stocknewsapi
DFLI
RENO, Nev., Nov. 25, 2025 (GLOBE NEWSWIRE) -- Dragonfly Energy Holdings Corp. (Nasdaq: DFLI) (“Dragonfly Energy” or the “Company”), an industry leader in energy storage and maker of Battle Born Batteries®, today announced a major expansion of its Battle Born® product portfolio. The Company is introducing new inverter/chargers, Base Series batteries, and a redesigned mobile app, strengthening its position as a complete power solutions provider across off-grid, RV, marine, and commercial markets.

The expansion includes the new Battle Born Inverter/Charger Series, which features pure sine wave models equipped with advanced power control and inverter assist functions for efficient and intelligent power management. Each unit is equipped with Dragonfly IntelLigence® technology and is compatible with the Battle Born mobile app, enabling real-time system monitoring, control, and visibility across multiple system components.

The Company is also launching the Battle Born Base Series Batteries bringing Battle Born reliability to a broader, value-conscious market. These smaller-capacity batteries are well-suited for a wide range of portable and auxiliary power needs, offering a modern LiFePO₄ alternative to traditional sealed lead-acid units.

In addition, Dragonfly Energy will release the Battle Born Mobile App V2.0. The updated app features a completely redesigned interface and an optimized backend for more accurate and intuitive system control. Users can view all Battle Born–branded components and batteries in one place, adjust settings in real time, and access detailed insights into system performance and battery health. The update expands compatibility across the ecosystem, supporting Battle Born batteries, inverter/chargers, and alternator regulators such as the Company’s Wakespeed® lineup. This new update introduces RV-C integration via the Battle Born HUB, a significant enhancement that enables seamless interoperability with major third-party platforms.

“Expanding our product ecosystem marks a pivotal moment in Dragonfly Energy’s evolution,” said Dr. Denis Phares, chief executive officer of Dragonfly Energy. “With our new inverter/chargers, Base Series batteries, and the redesigned Battle Born app, we are strengthening the capabilities of the entire Battle Born platform. Our focus is on delivering a fully integrated power system that we believe gives customers greater control, simplicity of use, and confidence in every application. This portfolio reflects the next chapter of the Battle Born brand and our commitment to long-term scalability and innovation.”

The new inverter/chargers and Base Series batteries are available for sale now as part of the Company’s annual Black Friday sales event. The Battle Born Mobile App V2.0 will launch on November 28, 2025, with additional product releases planned throughout 2026.

For more information about Dragonfly Energy and its innovative energy solutions, visit DragonflyEnergy.com. 

To shop and learn about the new Battle Born products, visit Battle-Born.com.

About Dragonfly Energy
Dragonfly Energy Holdings Corp. (Nasdaq: DFLI) is a comprehensive lithium battery technology company, specializing in cell manufacturing, battery pack assembly, and full system integration. Through its renowned Battle Born Batteries® brand, Dragonfly Energy has established itself as a frontrunner in the lithium battery industry, with hundreds of thousands of reliable battery packs deployed in the field through top-tier OEMs and a diverse retail customer base. At the forefront of domestic lithium battery cell production, Dragonfly Energy's patented dry electrode manufacturing process can deliver chemistry-agnostic power solutions for a broad spectrum of applications, including energy storage systems, electric vehicles, and consumer electronics. The Company's overarching mission is the future deployment of its proprietary, nonflammable, all-solid-state battery cells.

To learn more about Dragonfly Energy and its commitment to clean energy advancements, visit investors.dragonflyenergy.com.

Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the United States Private Securities Litigation Reform Act of 1995. Forward-looking statements include all statements that are not historical statements of fact and statements regarding the Company's intent, belief, or expectations, including, but not limited to, statements regarding the Company’s expansion of its Battle Born® product portfolio, Battle Born Batteries with Dragonfly IntelLigence, the Company's future results of operations and financial position, planned products and services, business strategy and plans, market size and growth opportunities, competitive position and technological and market trends. Some of these forward-looking statements can be identified by the use of forward-looking words, including "may," "should," "expect," "intend," "will," "estimate," "anticipate," "believe," "predict," "plan," "targets," "projects," "could," "would," "continue," "forecast" or the negatives of these terms or variations of them or similar expressions.

These forward-looking statements are subject to risks, uncertainties, and other factors (some of which are beyond the Company's control) which could cause actual results to differ materially from those expressed or implied by such forward-looking statements. Such factors include those set forth in the sections entitled "Risk Factors" and "Cautionary Note Regarding Forward-Looking Statements" in the Company's Annual Report on Form 10-K for the year ended December 31, 2024, and in the Company's subsequent filings with the SEC available at www.sec.gov. If any of these risks materialize or any of the Company's assumptions prove incorrect, actual results could differ materially from the results implied by these forward-looking statements. There may be additional risks that the Company presently does not know or that it currently believes are immaterial that could also cause actual results to differ from those contained in the forward-looking statements. All forward-looking statements contained in this press release speak only as of the date they were made. Except to the extent required by law, the Company undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made.

Photos:

Investor Relations
Eric Prouty
Szymon Serowiecki
AdvisIRy Partners
[email protected]

Media Relations
Margaret Skillicorn
RAD Strategies Inc.
[email protected]

Source: Dragonfly Energy Holdings Corp.
2025-11-25 12:53 5mo ago
2025-11-25 07:30 5mo ago
Parsons to Present at Goldman Sachs Industrials and Materials Conference stocknewsapi
PSN
November 25, 2025 07:30 ET

 | Source:

Parsons Services Company

CHANTILLY, Va., Nov. 25, 2025 (GLOBE NEWSWIRE) -- Parsons Corporation (NYSE: PSN) announced today that Carey Smith, chair, president, and chief executive officer, and Matt Ofilos, chief financial officer, will participate in a fireside chat question and answer session at the Goldman Sachs Industrials and Materials Conference on Wednesday, December 3, 2025, at approximately 2:10 p.m. Eastern Time.

The presentation will be available live via webcast on the investor relations section of Parsons’ website (https://investors.parsons.com). A replay of the webcast will be available on the website following the presentation for 30 days.

About Parsons Corporation

Parsons (NYSE: PSN) is a leading disruptive technology provider in the national security and global infrastructure markets, with capabilities across cyber and electronic warfare, space and missile defense, transportation, water and environment, urban development, and critical infrastructure protection. Please visit Parsons.com and follow us on LinkedIn to learn how we’re making an impact.

Contacts:
2025-11-25 12:53 5mo ago
2025-11-25 07:30 5mo ago
BriaCell to Highlight Positive Phase 2 & Phase 3 Clinical Data at SABCS® 2025 stocknewsapi
BCTX
November 25, 2025 07:30 ET

 | Source:

BriaCell Therapeutics Corp.

Three poster presentations at the San Antonio Breast Cancer Symposium (December 10, 2025) will highlight positive Phase 2 safety and efficacy signals and positive biomarker findings in both the Phase 2 and the pivotal Phase 3 studies The pivotal Phase 3 study of Bria-IMT+CPI is ongoing with an interim analysis expected in H1-2026The Bria-IMT regimen has received Fast Track Designation from US FDA
PHILADELPHIA and VANCOUVER, British Columbia, Nov. 25, 2025 (GLOBE NEWSWIRE) -- BriaCell Therapeutics Corp. (Nasdaq: BCTX, BCTXW) (TSX: BCT) (“BriaCell” or the “Company”), a clinical-stage biotechnology company developing novel immunotherapies to transform cancer care, will present positive biomarker and survival data across three clinical posters at the 2025 San Antonio Breast Cancer Symposium (SABCS®) taking place December 9-12, 2025 at Henry B. Gonzalez Convention Center, 900 E. Market Street, San Antonio, Texas.

“Positive clinical data from our Phase 2 study, together with differentiated biomarker findings from our Phase 3 program reinforce our confidence in our pivotal Phase 3 study in metastatic breast cancer,” stated William V. Williams, MD, BriaCell’s President & CEO. “Together with our pipeline of novel off-the-shelf cell-based immunotherapies, we remain committed to advancing breakthroughs in cancer immunotherapy as we work to improve survival and clinical outcomes in cancer patients with unmet medical needs.”

“Our biomarker data provides important insights into the mechanism of action of our novel immunotherapy with the goal of delivering more precisely targeted treatment options for oncologists, physicians, and patients,” commented Miguel A. Lopez-Lago, PhD, BriaCell’s Chief Scientific Officer.

Late-Breaking Abstract Number: 3688
Presentation Number: PS1-13-22
Presentation Title: Impact of Prior Therapy, Genotype Matching, and Biomarkers in the Bria-ABC Phase 3 Trial
Poster Presentation Date/Time: Wednesday, December 10, 2025, 12:30 PM - 2:00 PM CST

Late-Breaking Abstract Number: 3713
Presentation Number: PS1-13-23
Presentation Title: Survival Results of Phase II Bria-IMT Allogenic Whole Cell-Based Cancer Vaccine
Poster Presentation Date/Time: Wednesday, December 10, 2025, 12:30 PM - 2:00 PM CST

Abstract Number: 1614
Presentation Number: PS2-09-03
Presentation Title: Th1-biased cytokine signatures as biomarkers of clinical benefit following SV-BR-1-GM cancer vaccination in breast cancer.
Poster Presentation Date/Time: Wednesday, December 10, 2025, 5:00 PM - 6:30 PM CST

Copies of the abstracts and posters will be made available at https://briacell.com/scientific-publications/.

About BriaCell Therapeutics Corp.

BriaCell is a clinical-stage biotechnology company that develops novel immunotherapies to transform cancer care. More information is available at https://briacell.com/.

Safe Harbor

This press release contains “forward-looking statements” that are subject to substantial risks and uncertainties. All statements, other than statements of historical fact, contained in this press release are forward-looking statements. Forward-looking statements contained in this press release may be identified by the use of words such as “anticipate,” “believe,” “contemplate,” “could,” “estimate,” “expect,” “intend,” “seek,” “may,” “might,” “plan,” “potential,” “predict,” “project,” “target,” “aim,” “should,” “will,” “would,” or the negative of these words or other similar expressions, although not all forward-looking statements contain these words. Forward-looking statements, including those about presenting three posters at the 2025 SABCS, and the contents of such posters, are based on BriaCell’s current expectations and are subject to inherent uncertainties, risks, and assumptions that are difficult to predict. Further, certain forward-looking statements are based on assumptions as to future events that may not prove to be accurate. These and other risks and uncertainties are described more fully under the heading “Risks and Uncertainties” in the Company's most recent Management’s Discussion and Analysis, under the heading "Risk Factors" in the Company's most recent Annual Information Form, and under “Risks and Uncertainties” in the Company's other filings with the Canadian securities regulatory authorities and the U.S. Securities and Exchange Commission, all of which are available under the Company's profiles on SEDAR+ at www.sedarplus.ca and on EDGAR at www.sec.gov. Forward-looking statements contained in this announcement are made as of this date, and BriaCell Therapeutics Corp. undertakes no duty to update such information except as required under applicable law.

Neither the Toronto Stock Exchange nor its Regulation Services Provider (as that term is defined in the policies of the Toronto Stock Exchange) accepts responsibility for the adequacy or accuracy of this release.

Contact Information

Company Contact:
William V. Williams, MD
President & CEO
1-888-485-6340
[email protected] 

Investor Relations Contact:
[email protected]
2025-11-25 12:53 5mo ago
2025-11-25 07:30 5mo ago
Abercrombie & Fitch Co. Reports Third Quarter Fiscal 2025 Results stocknewsapi
ANF
Record third quarter net sales of $1.3 billion, up 7% from last year, 12th consecutive quarter of growthNet sales growth led by Americas up 7%, EMEA up 7%, partially offset by 6% decline in APACBrand performance led by Hollister brands growth of 16%, with Abercrombie brands down 2%Operating margin of 12.0%, with earnings per diluted share of $2.36 exceeding outlook range$100 million in shares repurchased in the quarter; Year-to-date share repurchases of $350 million, 9% of shares outstanding at beginning of the yearNarrows full-year outlook to net sales growth of 6% to 7%, net income per diluted share of $10.20 to $10.50 NEW ALBANY, Ohio, Nov. 25, 2025 (GLOBE NEWSWIRE) -- Abercrombie & Fitch Co. (NYSE: ANF) today announced results for the third quarter ended November 1, 2025. These compare to results for the third quarter ended November 2, 2024. Descriptions of the use of non-GAAP financial measures and reconciliations of GAAP and non-GAAP financial measures accompany this release.

Fran Horowitz, Chief Executive Officer, said, “We achieved three years of consecutive quarterly sales growth, delivering record third quarter net sales, with 7% growth to last year. Hollister brands grew 16% on a strong finish to back-to-school and fall seasonal transition. Abercrombie brands made sequential progress in-line with our expectations, and we are tightly managing inventory as we aim for fourth quarter brand net sales to be approximately flat to last year’s record. On the bottom line, we delivered a 12.0% operating margin including important investments in marketing, digital and technology, in addition to 210 basis points of adverse tariff impact. We exceeded our expectations on earnings per share, while also returning $100 million to shareholders in the third quarter, our seventh consecutive quarter of share repurchases.  

As we enter the holiday season, our global teams are energized and ready to deliver exceptional experiences for our customers across brands and regions. We remain on track toward record net sales for fiscal 2025, on the foundation of consistent quarterly top-line growth, top-tier profitability, and healthy cash flow. Our results reinforce the strength of our operating model and give us confidence in our ability to drive sustainable, long-term shareholder value.”

Details related to reported net income per diluted share and adjusted net income per diluted share for the third quarter are as follows:

   2025  2024 GAAP $2.36 $2.50 Impact from changes in foreign currency exchange rates(1)  —  (0.03)Adjusted non-GAAP constant currency $2.36 $2.47  (1)  The estimated impact from foreign currency is calculated by applying current period exchange rates to prior year results using a 26% tax rate.

A summary of results for the third quarter ended November 1, 2025 as compared to the third quarter ended November 2, 2024:

Net sales of $1.3 billion, up 7% as compared to last year, with comparable sales of 3%.Operating income of $155 million as compared to operating income last year of $179 million.Operating margin as a percent of sales of 12.0% as compared to 14.8% last year.Net income per diluted share of $2.36 as compared to net income per diluted share last year of $2.50. Net Sales

Net sales by segment and brand for the third quarter are as follows:

(in thousands) 2025  2024 1 YR % Change Comparable sales(2)Net sales by segment:(1)       Americas(3)$1,057,448 $986,449 7% 4%EMEA(4) 194,510  181,592 7% 2%APAC(5) 38,661  40,925 (6)% (12)%Total company$1,290,619 $1,208,966 7% 3%          2025  2024 1 YR % Change Comparable sales(2)Net sales by brand family:       Abercrombie$617,345 $629,835 (2)% (7)%Hollister 673,274  579,131 16% 15%Total company$1,290,619 $1,208,966 7% 3% (1) Net sales by segment are presented by attributing revenues to a physical store location or geographical region that fulfills the order.
(2) Comparable sales are calculated on a constant currency basis. Refer to "REPORTING AND USE OF GAAP AND NON-GAAP MEASURES," for further discussion.
(3) The Americas segment includes the results of operations in North America and South America.
(4) The EMEA segment includes the results of operations in Europe, the Middle East and Africa.
(5) The APAC segment includes the results of operations in the Asia-Pacific region, including Asia and Oceania.

Financial Position and Liquidity

As of November 1, 2025 the company had:

Cash and equivalents of $606 million compared to $773 million and $683 million as of February 1, 2025 and November 2, 2024, respectively.Marketable securities of $25 million compared to $116 million and $56 million as of February 1, 2025 and November 2, 2024, respectively. The decrease from February 1, 2025 was due to $105 million of maturities in Fiscal 2025.Inventories of $730 million compared to $575 million and $693 million as of February 1, 2025 and November 2, 2024, respectively.Borrowing capacity of $500 million under the senior-secured asset-based revolving credit facility (the “ABL Facility”) with net borrowing available of $450 million after minimum excess availability requirement.Liquidity comprised of cash and equivalents and borrowing available under the ABL Facility, of approximately $1.1 billion as of November 1, 2025. This compares to liquidity of $1.2 billion and $1.1 billion as of February 1, 2025 and November 2, 2024, respectively. Cash Flow and Capital Allocation

Details related to the company’s cash flows for the year-to-date period ended November 1, 2025 are as follows:

Net cash provided by operating activities of $313 million.Net cash used for investing activities of $95 million, primarily reflecting capital expenditures, partially offset by maturities of marketable securities.Net cash used for financing activities of $395 million, primarily reflecting share repurchases.
During the third quarter of 2025, the company repurchased 1.2 million shares for approximately $100 million. For the year-to-date period ended November 1, 2025, the company repurchased 4.5 million shares for $350 million, representing a 9% reduction in shares outstanding from the beginning of the year. The company has $950 million remaining on the share repurchase authorization established in March 2025.

Depreciation and amortization was $115 million for the year-to-date period ended November 1, 2025.

Fiscal 2025 Outlook

The following outlook replaces all previous full year guidance. For fiscal 2025, the company now expects: Current Full Year Outlook(1) (2)Previous Full Year Outlook(2)(3)Net salesGrowth In The Range of 6% to 7%Growth In The Range of 5% to 7%Operating marginIn The Range of 13.0% to 13.5%In The Range of 13.0% to 13.5%Effective tax rate(4)Around 30%Around 30%Net income per diluted share(5) (6)In The Range of $10.20 to $10.50In The Range of $10.00 to $10.50Share repurchases(6)Around $450 millionAround $400 millionDiluted weighted average shares(5) (6)Around 48 millionAround 49 millionCapital expenditures~$225 million~$225 millionReal estate activity
~40 Net Store Openings~40 Net Store Openings(all approximate)60 Openings, 20 Closures60 Openings, 20 Closures 40 Remodels And Right-Sizes40 Remodels And Right-Sizes     FourthQuarter Outlook(1) Net salesGrowth In The Range of 4% to 6% Operating marginAround 14% Effective tax rate(4)Around 30% Net income per diluted share(5) (6)In The Range of $3.40 to $3.70 Share repurchases(6)Around $100 million Diluted weighted average shares(5) (6)Around 47 million  (1) Includes the estimated impact from the tariffs on goods imported into the United States in accordance with trade policies as of November 21, 2025. This excludes any other potential future trade policy changes imposed by the United States or other countries. Net of planned mitigation efforts, the full year outlook assumes approximately $90 million of tariff expense, or 170 basis points as a percent of net sales.
(2) Includes $39 million net benefit on a pre-tax basis, or $29 million on a tax-adjusted basis, from a litigation settlement.
(3) Released August 27, 2025.
(4) The current outlook for effective tax rate is sensitive to the jurisdictional mix and level of income and does not include the impact of potential future tax policy or legislative changes.
(5) The current outlook for net income per diluted share and diluted weighted average shares includes the anticipated impact to shares outstanding from potential share repurchase activity in fiscal 2025.
(6) The timing and amount of any such repurchases will be determined based on an evaluation of market conditions, the company’s share price, legal requirements, and other factors.

Conference Call

Today at 8:30 a.m. ET, the company will conduct a conference call and provide additional details around its quarterly results and its outlook for the fourth quarter. To access the call by phone, participants will need to register at the following URL address to obtain a dial-in number and passcode:

https://register-conf.media-server.com/register/BI2e64b4f132384c58afdebae36de224c2 

A presentation of third quarter results will be available in the “Investors” section at corporate.abercrombie.com at approximately 7:30 a.m. ET, today. Important information may be disseminated initially or exclusively via the website; investors should consult the site to access this information.

Safe Harbor Statement Under the Private Securities Litigation Reform Act of 1995

This Press Release and related statements by management or spokespeople of Abercrombie & Fitch Co. (A&F) contain forward-looking statements (as such term is defined in the Private Securities Litigation Reform Act of 1995). These statements, including, without limitation, statements regarding our fourth quarter and annual fiscal 2025 results, relate to our current assumptions, projections and expectations about our business and future events. Any such forward-looking statements involve risks and uncertainties and are subject to change based on various important factors, many of which may be beyond the company’s control. The inclusion of such information should not be regarded as a representation by the company, or any other person, that the objectives of the company will be achieved. Words such as “estimate,” “project,” “plan,” “goal,” “believe,” “expect,” “anticipate,” “intend,” “should,” “are confident,” “will,” “could,” “outlook,” and similar expressions may identify forward-looking statements. Except as may be required by applicable law, we assume no obligation to publicly update or revise any forward-looking statements, including any financial targets, estimates, or performance outlooks whether as a result of new information, future events, or otherwise. Factors that may cause results to differ from those expressed in our forward-looking statements include, but are not limited to, the factors disclosed in Part I, Item 1A. “Risk Factors” of the company’s Annual Report on Form 10-K for the fiscal year ended February 1, 2025, and in our subsequent reports and filings with the Securities and Exchange Commission, as well as the following factors: risks and uncertainties related to global trade policy and global trade disputes, including the impact of the imposition or threat of imposition of new or increased tariffs by the United States or foreign governments or other changes to trade policies and arrangements; risks related to changes in global economic and financial conditions, including inflation, and the resulting impact on consumer spending and our operating results, financial condition, and expense management; risks related to global operations, including changes in the economic or political conditions where we sell or source our products; risks related to the geopolitical landscape and ongoing armed conflicts, acts of terrorism, mass casualty events, social unrest, civil disturbance or disobedience and the impact of such conflicts or events on international trade, supplier delivery or increased freight costs; risks related to natural disasters and other unforeseen catastrophic events; risks related to our failure to engage our customers, anticipate customer demand, expectations, and changing fashion trends, and manage our inventory and product delivery; risks related to our failure to operate effectively in a highly competitive and constantly evolving industry; risks related to our ability to successfully invest in and execute on our customer, digital and omnichannel initiatives; risks related to our ability to successfully execute technology initiatives and partnerships, such as those relating to artificial intelligence technology; risks related to our ability to execute on, and maintain the success of, our strategic and growth initiatives; risks related to fluctuations in foreign currency exchange rates; risks related to fluctuations in our tax obligations and effective tax rate, including as a result of earnings and losses generated from our global operations, may result in volatility in our results of operations; risks and uncertainty related to adverse public health developments; risks associated with climate change and other corporate responsibility issues; risks related to reputational harm to the company, its officers, and directors; risks related to actual or threatened litigation; risks related to cybersecurity threats and privacy or data security breaches, and the potential loss or disruption to our information systems, and uncertainties related to future legislation, regulatory reform, policy changes, or interpretive guidance on existing laws and regulations.

Other Information

This document includes certain adjusted non-GAAP financial measures, which are not calculated in accordance with accounting principles generally accepted in the United States of America (“GAAP”) and exclude the impact of certain items. Management uses these non-GAAP financial measures to evaluate the company’s performance and manage its operations, and believes such measures to be helpful in understanding the company's results of operations or financial position. These non-GAAP financial measures are intended to complement, and are not considered as alternatives to, the most directly comparable GAAP financial measures, as reconciled in the above table. Also, such non-GAAP financial measures may not be comparable to similarly titled measures used by other entities. Additional details about non-GAAP financial measures and a reconciliation of GAAP financial measures to non-GAAP financial measures can be found in the “Reporting and Use of GAAP and Non-GAAP Measures” section. Sub-totals and totals may not foot due to rounding. Net income and net income per share financial measures included herein are attributable to Abercrombie & Fitch Co., excluding net income attributable to noncontrolling interests.

As used in this document, references to “Americas” includes North America and South America, “EMEA” includes Europe, the Middle East and Africa and “APAC” includes the Asia-Pacific region, including Asia and Oceania.

About Abercrombie & Fitch Co.

Abercrombie & Fitch Co. (NYSE: ANF) is a global, digitally led, omnichannel specialty retailer of apparel and accessories catering to kids through millennials with assortments curated for their specific lifestyle needs.

The company operates a family of brands, including Abercrombie brands and Hollister brands, each sharing a commitment to offer products of enduring quality and exceptional comfort that support global customers on their journey to being and becoming who they are. Abercrombie & Fitch Co. operates approximately 830 stores under these brands across North America, Europe, Asia and the Middle East, as well as the e-commerce sites abercrombie.com, abercrombiekids.com, and HollisterCo.com.

Investor Contact:Media Contact:  Mo GuptaKate WagnerAbercrombie & Fitch Co.Abercrombie & Fitch Co.(614) 283-6751(614) [email protected][email protected] Abercrombie & Fitch Co.Condensed Consolidated Statements of Operations(in thousands, except per share data)(Unaudited)         Thirteen Weeks Ended Thirteen Weeks Ended November 1, 2025 % of
Net Sales November 2, 2024 % of
Net SalesNet sales$1,290,619  100.0% $1,208,966  100.0%Cost of sales, exclusive of depreciation and amortization 483,670  37.5%  422,034  34.9%Selling expense 459,548  35.6%  420,990  34.8%General and administrative expense 193,402  15.0%  188,246  15.6%Other operating income, net (1,022) (0.1)%  (1,586) (0.1)%Operating income 155,021  12.0%  179,282  14.8%Interest expense 550  —%  569  —%Interest income (6,491) (0.5)%  (9,302) (0.8)%Interest income, net (5,941) (0.5)%  (8,733) (0.7)%Income before income taxes 160,962  12.5%  188,015  15.6%Income tax expense 45,862  3.6%  54,151  4.5%Net income 115,100  8.9%  133,864  11.1%Less: Net income attributable to noncontrolling interests 2,105  0.2%  1,885  0.2%Net income attributable to A&F$112,995  8.8% $131,979  10.9%        Net income per share attributable to A&F       Basic$2.41    $2.59   Diluted$2.36    $2.50           Weighted-average shares outstanding:       Basic 46,842     50,951   Diluted 47,881     52,869    Abercrombie & Fitch Co.Condensed Consolidated Statements of Operations(in thousands, except per share data)(Unaudited)         Thirty-Nine Weeks Ended Thirty-Nine Weeks Ended November 1, 2025 % of
Net Sales November 2, 2024 % of
Net SalesNet sales$3,596,490  100.0% $3,363,670  100.0%Cost of sales, exclusive of depreciation and amortization 1,352,393  37.6%  1,163,019  34.6%Selling expense 1,234,841  34.3%  1,163,565  34.6%General and administrative expense 543,652  15.1%  555,941  16.5%Other operating loss (income), net 2,392  0.1%  (3,611) (0.1)%Operating income 463,212  12.9%  484,756  14.4%Interest expense 1,831  0.1%  11,538  0.3%Interest income (17,029) (0.5)%  (30,497) (0.9)%Interest income, net (15,198) (0.4)%  (18,959) (0.6)%Income before income taxes 478,410  13.3%  503,715  15.0%Income tax expense 138,183  3.8%  119,394  3.5%Net income 340,227  9.5%  384,321  11.4%Less: Net income attributable to noncontrolling interests 5,436  0.2%  5,324  0.2%Net income attributable to A&F$334,791  9.3% $378,997  11.3%        Net income per share attributable to A&F       Basic$6.99    $7.43   Diluted$6.83    $7.13           Weighted-average shares outstanding:       Basic 47,869     51,030   Diluted 49,022     53,141    Reporting and Use of GAAP and Non-GAAP Measures

The company believes that each of the non-GAAP financial measures presented are useful to investors as they provide a measure of the company’s operating performance excluding the effect of certain items which the company believes do not reflect its future operating outlook, therefore supplementing investors’ understanding of comparability of operations across periods. Management used these non-GAAP financial measures during the periods presented to assess the company’s performance and to develop expectations for future operating performance. Non-GAAP financial measures should be used supplementally to, and not as an alternative to, the company’s GAAP financial results, and may not be calculated in the same manner as similar measures presented by other companies.

The company provides comparable sales, defined as the percentage year-over-year change in the aggregate of: (1) sales for stores that have been open as the same brand at least one year and whose square footage has not been expanded or reduced by more than 20% within the past year, with prior year’s net sales converted at the current year’s foreign currency exchange rate to remove the impact of foreign currency rate fluctuation, and (2) digital net sales with prior year’s net sales converted at the current year’s foreign currency exchange rate to remove the impact of foreign currency rate fluctuation.

The company also provides certain financial information on a constant currency basis to enhance investors’ understanding of underlying business trends and operating performance, by removing the impact of foreign currency exchange rate fluctuations. The effect from foreign currency, calculated on a constant currency basis, is determined by applying current year average exchange rates to prior year results and is net of the year-over-year impact from hedging. The per diluted share effect from foreign currency is calculated using a 26% tax rate.

In addition, the company provides EBITDA and Adjusted EBITDA as supplemental measures used by the company’s executive management to assess the company’s performance. We also believe these supplemental performance measures are meaningful information for investors and other interested parties to use in computing the company’s core financial performance over multiple periods and with other companies by excluding the impact of differences in tax jurisdictions, debt service levels and capital investment.

Abercrombie & Fitch Co.Schedule of Non-GAAP Financial MeasuresThirty-Nine Weeks Ended November 1, 2025(in thousands, except per share data)(Unaudited)           GAAP(1) % of
Net Sales Excluded item(2) Adjusted
non-GAAP % of
Net SalesLitigation settlement$(38,574)   $(38,574) $—  Operating income 463,212  12.9%  38,574   424,638 11.8%Income before income taxes 478,410  13.3%  38,574   439,836 12.2%Income tax expense(3) 138,183  3.8%  9,829   128,354 3.6%Net income attributable to A&F 334,791  9.3%  28,745   306,046 8.5%          Net income per diluted share attributable to A&F$6.83    $0.59  $6.24  Diluted weighted-average shares outstanding 49,022       49,022   (1) “GAAP” refers to accounting principles generally accepted in the United States of America.
(2) Excluded item consists of a favorable settlement, net of legal fees, of payment card interchange fee litigation
(3) The tax effect of excluded items is the difference between the tax provision calculated on a GAAP basis and an adjusted non-GAAP basis.

Abercrombie & Fitch Co.Reconciliation of Constant Currency Financial MeasuresThirteen Weeks Ended November 1, 2025 and November 2, 2024(in thousands, except percentage and basis point changes and per share data)(Unaudited)        2025  2024  % ChangeNet sales     GAAP(1)$1,290,619 $1,208,966   7% Impact from changes in foreign currency exchange rates(2) —  5,834   — Net sales on a constant currency basis$1,290,619 $1,214,800   6%       Operating income 2025  2024  BPS Change(3)GAAP(1)$155,021 $179,282   (280) Impact from changes in foreign currency exchange rates(2) —  (1,852)  20 Non-GAAP constant currency basis$155,021 $177,430   (260)       Net income per share attributable to A&F 2025  2024  $ ChangeGAAP(1)$2.36 $2.50  $(0.14) Impact from changes in foreign currency exchange rates(2) —  (0.03)  0.03 Non-GAAP constant currency basis$2.36 $2.47  $(0.11)  (1) “GAAP” refers to accounting principles generally accepted in the United States of America.
(2) The estimated impact from foreign currency is determined by applying current period exchange rates to prior year results and is net of the year-over-year impact from hedging. The per diluted share estimated impact from foreign currency is calculated using a 26% tax rate.
(3) The estimated basis point change has been rounded based on the percentage change.

Abercrombie & Fitch Co.Reconciliation of EBITDA and Adjusted EBITDAThirteen Weeks Ended November 1, 2025 and November 2, 2024(in thousands)(Unaudited)         2025  % of
Net Sales 2024  % of
Net SalesNet income$115,100  8.9%$133,864  11.1%Income tax expense 45,862  3.6  54,151  4.5 Interest income, net (5,941) (0.5) (8,733) (0.7)Depreciation and amortization 38,566  3.0  39,566  3.2 EBITDA$193,587  15.0%$218,848  18.1%              Abercrombie & Fitch Co.Reconciliation of EBITDA and Adjusted EBITDAThirty-Nine Weeks Ended November 1, 2025 and November 2, 2024(in thousands)(Unaudited)         2025  % of
Net Sales 2024  % of
Net SalesNet income$340,227  9.5%$384,321  11.4%Income tax expense 138,183  3.8  119,394  3.5 Interest (income) expense, net (15,198) (0.4) (18,959) (0.6)Depreciation and amortization 114,566  3.2  116,610  3.6 EBITDA(1)$577,778  16.1%$601,366  17.9%       Adjustments to EBITDA      Litigation settlement (38,574) (1.1)% —  —%Adjusted EBITDA(1)$539,204  15.0%$601,366  17.9% (1) EBITDA and Adjusted EBITDA are supplemental financial measures that are not defined or prepared in accordance with GAAP. EBITDA is defined as net income before interest, income taxes and depreciation and amortization. Adjusted EBITDA is EBITDA adjusted for a favorable settlement, net of legal fees, of payment card interchange fee litigation.

Abercrombie & Fitch Co.Condensed Consolidated Balance Sheets(in thousands)(Unaudited)       November 1, 2025 February 1, 2025 November 2, 2024Assets     Current assets:     Cash and equivalents$605,783 $772,727 $683,089Marketable securities 25,255  116,221  55,790Receivables 131,741  105,324  111,583Inventories 730,453  575,005  692,596Other current assets 116,303  104,154  112,709Total current assets 1,609,535  1,673,431  1,655,767Property and equipment, net 661,646  575,773  570,440Operating lease right-of-use assets 965,919  803,121  798,290Other assets 242,818  247,562  245,375Total assets$3,479,918 $3,299,887 $3,269,872      Liabilities and stockholders’ equity     Current liabilities:     Accounts payable$461,528 $364,532 $466,303Accrued expenses 458,075  504,922  469,148Short-term portion of operating lease liabilities 225,847  211,600  210,335Income taxes payable 17,557  45,890  36,303Total current liabilities$1,163,007 $1,126,944 $1,182,089Long-term liabilities:     Long-term portion of operating lease liabilities$905,041 $740,013 $734,918Other liabilities 80,460  81,607  92,405Total long-term liabilities 985,501  821,620  827,323Total Abercrombie & Fitch Co. stockholders’ equity 1,316,843  1,335,628  1,247,133Noncontrolling interests 14,567  15,695  13,327Total stockholders’ equity 1,331,410  1,351,323  1,260,460Total liabilities and stockholders’ equity$3,479,918 $3,299,887 $3,269,872 Abercrombie & Fitch Co.Condensed Consolidated Statements of Cash Flows(in thousands, except per share data)(Unaudited)         Thirty-Nine Weeks Ended November 1, 2025 November 2, 2024Operating activities   Net cash provided by operating activities$313,000  $402,756     Investing activities   Purchases of marketable securities$(15,000) $(55,000)Proceeds from maturities of marketable securities 105,000   — Purchases of property and equipment (185,212)  (132,040)Net cash used for investing activities$(95,212) $(187,040)    Financing activities   Redemption of senior secured notes$—  $(223,331)Payment of debt modification costs and fees —   (3,273)Purchases of common stock (351,224)  (129,807)Acquisition of common stock for tax withholding obligations (36,181)  (69,613)Other financing activities (7,149)  (6,546)Net cash used for financing activities$(394,554) $(432,570)    Effect of foreign currency exchange rates on cash$8,930  $(1,834)Net decrease in cash and equivalents, and restricted cash and equivalents$(167,836) $(218,688)Cash and equivalents, and restricted cash and equivalents, beginning of period$780,395  $909,685 Cash and equivalents, and restricted cash and equivalents, end of period$612,559  $690,997 
2025-11-25 12:53 5mo ago
2025-11-25 07:30 5mo ago
Eisai Completes Rolling Submission to US FDA for LEQEMBI® IQLIK™ (lecanemab-irmb) Supplemental Biologics License Application as a Subcutaneous Starting Dose for the Treatment of Early Alzheimer's Disease Under Fast Track Status stocknewsapi
BIIB
LEQEMBI IQLIK, if approved for initiation dosing, would be the first and only anti-amyloid treatment to offer at-home injection from the start of therapy to help patients and care partners treat this progressive, relentless disease

November 25, 2025 07:30 ET

 | Source:

Biogen Inc.; Eisai Co., Ltd.

TOKYO and CAMBRIDGE, Mass., Nov. 25, 2025 (GLOBE NEWSWIRE) -- Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo Naito, “Eisai”) and Biogen Inc. (Nasdaq: BIIB, Corporate headquarters: Cambridge, Massachusetts, CEO: Christopher A. Viehbacher, “Biogen”) announced today that Eisai has completed the rolling submission of the Supplemental Biologics License Application (sBLA) to the U.S. Food and Drug Administration (FDA) for lecanemab-irmb (U.S. brand name: LEQEMBI®) subcutaneous autoinjector (SC-AI), LEQEMBI IQLIK, as a weekly starting dose after the FDA granted Fast Track Status. LEQEMBI is indicated for the treatment of Alzheimer’s disease (AD) in patients with Mild Cognitive Impairment (MCI) or mild dementia stage of disease (collectively referred to as early AD). Upon acceptance of the sBLA, the FDA will set a Prescription Drug User Fee Act (PDUFA) action date (target date for review completion).

The sBLA is supported by data evaluating subcutaneous (SC) administration of lecanemab across a range of doses and as part of sub-studies within the Phase 3 Clarity AD open-label extension (OLE) following the 18-month core study in individuals with early AD. Data show that once-weekly administration of the 500 mg of SC-AI achieved equivalent exposure to once every two weeks intravenous (IV) administration and similar clinical and biomarker benefits. Subcutaneous administration demonstrated a safety profile similar to IV administration, with less than 2% incidence of systemic injection/infusion-related reactions.

Should the FDA approve the LEQEMBI IQLIK 500 mg SC dosing regimen (two 250 mg injections), the autoinjector could be used to administer a once-weekly starting dose, as an alternative to the current bi-weekly (every two weeks) intravenous (IV) dosing. This would enable patients and care partners to choose SC administration at home for both initial treatment and the currently approved maintenance therapy, offering the option of SC or IV administration throughout the entire treatment journey. The injection time for each LEQEMBI IQLIK autoinjector takes approximately 15 seconds. The SC formulation also has the potential to reduce healthcare resources associated with IV dosing, such as preparation for infusion and nurse monitoring, while streamlining the overall AD treatment pathway.

AD is a progressive, relentless disease, with amyloid beta (Aβ) and tau as hallmarks, that is caused by a continuous underlying neurotoxic process driven by protofibrils* that begins before amyloid plaque accumulation and continues after plaque removal.1,2,3 Only LEQEMBI fights AD in two ways – targeting both protofibrils and amyloid plaque, which can impact tau downstream.

LEQEMBI is currently approved in 51 countries and regions and is under regulatory review in 9 countries. In August 2025, the US FDA approved LEQEMBI IQLIK 360 mg for weekly subcutaneous maintenance dosing after 18 months of IV treatment every two weeks.

Eisai serves as the lead for lecanemab’s development and regulatory submissions globally with Eisai and Biogen co-commercializing and co-promoting the product and Eisai having final decision-making authority.

*Protofibrils are believed to contribute to the brain injury that occurs with AD and are considered to be the most toxic form of Aβ, having a primary role in the cognitive decline associated with this progressive, debilitating condition.1 Protofibrils cause injury to neurons in the brain, which in turn, can negatively impact cognitive function via multiple mechanisms, not only increasing the development of insoluble Aβ plaques but also increasing direct damage to brain cell membranes and the connections that transmit signals between nerve cells or nerve cells and other cells. It is believed the reduction of protofibrils may prevent the progression of AD by reducing damage to neurons in the brain and cognitive dysfunction.2 

INDICATION
LEQEMBI® is indicated for the treatment of Alzheimer’s disease (AD). Treatment with LEQEMBI should be initiated in patients with mild cognitive impairment (MCI) or mild dementia stage of disease, the population in which treatment was initiated in clinical trials.

IMPORTANT SAFETY INFORMATION

WARNING: AMYLOID-RELATED IMAGING ABNORMALITIES (ARIA) Monoclonal antibodies directed against aggregated forms of beta amyloid, including LEQEMBI, can cause ARIA, characterized as ARIA with edema (ARIA-E) and ARIA with hemosiderin deposition (ARIA-H). Incidence and timing of ARIA vary among treatments. ARIA usually occurs early in treatment and is usually asymptomatic, although serious and life-threatening events, including seizure and status epilepticus, can occur. ARIA can be fatal. Serious intracerebral hemorrhages (ICH) >1 cm, some of which have been fatal, have been observed with this class of medications. Because ARIA-E can cause focal neurologic deficits that can mimic an ischemic stroke, consider whether such symptoms could be due to ARIA-E before giving thrombolytic therapy to a patient being treated with LEQEMBI. Apolipoprotein E ε4 (ApoE ε4) Homozygotes: Patients who are ApoE ε4 homozygotes (~15% of patients with AD) treated with this class of medications have a higher incidence of ARIA, including symptomatic, serious, and severe radiographic ARIA, compared to heterozygotes and noncarriers. Testing for ApoE ε4 status should be performed prior to initiation of treatment to inform the risk of developing ARIA. Prior to testing, prescribers should discuss with patients the risk of ARIA across genotypes and the implications of genetic testing results. Prescribers should inform patients that if genotype testing is not performed, they can still be treated with LEQEMBI; however, it cannot be determined if they are ApoE ε4 homozygotes and at higher risk for ARIA. Consider the benefit of LEQEMBI for the treatment of AD and the potential risk of serious ARIA events when deciding to initiate treatment with LEQEMBI.   CONTRAINDICATION
Contraindicated in patients with serious hypersensitivity to lecanemab-irmb or to any of the excipients. Reactions have included angioedema and anaphylaxis.

WARNINGS AND PRECAUTIONS

Amyloid-Related Imaging Abnormalities
Medications in this class, including LEQEMBI, can cause ARIA-E, which can be observed on MRI as brain edema or sulcal effusions, and ARIA-H, which includes microhemorrhage and superficial siderosis. ARIA can occur spontaneously in patients with AD, particularly in patients with MRI findings suggestive of cerebral amyloid angiopathy (CAA), such as pretreatment microhemorrhage or superficial siderosis. ARIA-H generally occurs with ARIA-E. Reported ARIA symptoms may include headache, confusion, visual changes, dizziness, nausea, and gait difficulty. Focal neurologic deficits may also occur. Symptoms usually resolve over time.

Incidence of ARIA
Symptomatic ARIA occurred in 3% and serious ARIA symptoms in 0.7% with LEQEMBI. Clinical ARIA symptoms resolved in 79% of patients during the period of observation. ARIA, including asymptomatic radiographic events, was observed: LEQEMBI, 21%; placebo, 9%. ARIA-E was observed: LEQEMBI, 13%; placebo, 2%. ARIA-H was observed: LEQEMBI, 17%; placebo, 9%. No increase in isolated ARIA-H was observed for LEQEMBI vs placebo.

Incidence of ICH
ICH >1 cm in diameter was reported in 0.7% with LEQEMBI vs 0.1% with placebo. Fatal events of ICH in patients taking LEQEMBI have been observed.

Risk Factors of ARIA and ICH

ApoE ε4 Carrier Status
Of the patients taking LEQEMBI, 16% were ApoE ε4 homozygotes, 53% were heterozygotes, and 31% were noncarriers. With LEQEMBI, ARIA was higher in ApoE ε4 homozygotes (LEQEMBI: 45%; placebo: 22%) than in heterozygotes (LEQEMBI: 19%; placebo: 9%) and noncarriers (LEQEMBI: 13%; placebo: 4%). Symptomatic ARIA-E occurred in 9% of ApoE ε4 homozygotes vs 2% of heterozygotes and 1% of noncarriers. Serious ARIA events occurred in 3% of ApoE ε4 homozygotes and in ~1% of heterozygotes and noncarriers. The recommendations on management of ARIA do not differ between ApoE ε4 carriers and noncarriers.

Radiographic Findings of CAA
Neuroimaging findings that may indicate CAA include evidence of prior ICH, cerebral microhemorrhage, and cortical superficial siderosis. CAA has an increased risk for ICH. The presence of an ApoE ε4 allele is also associated with CAA.

The baseline presence of at least 2 microhemorrhages or the presence of at least 1 area of superficial siderosis on MRI, which may be suggestive of CAA, have been identified as risk factors for ARIA. Patients were excluded from Clarity AD for the presence of >4 microhemorrhages and additional findings suggestive of CAA (prior cerebral hemorrhage >1 cm in greatest diameter, superficial siderosis, vasogenic edema) or other lesions (aneurysm, vascular malformation) that could potentially increase the risk of ICH.

Concomitant Antithrombotic or Thrombolytic Medication
In Clarity AD, baseline use of antithrombotic medication (aspirin, other antiplatelets, or anticoagulants) was allowed if the patient was on a stable dose. Most exposures were to aspirin. Antithrombotic medications did not increase the risk of ARIA with LEQEMBI. The incidence of ICH: 0.9% in patients taking LEQEMBI with a concomitant antithrombotic medication vs 0.6% with no antithrombotic and 2.5% in patients taking LEQEMBI with an anticoagulant alone or with antiplatelet medication such as aspirin vs none in patients receiving placebo.

Fatal cerebral hemorrhage has occurred in 1 patient taking an anti-amyloid monoclonal antibody in the setting of focal neurologic symptoms of ARIA and the use of a thrombolytic agent.

Additional caution should be exercised when considering the administration of antithrombotics or a thrombolytic agent (e.g., tissue plasminogen activator) to a patient already being treated with LEQEMBI. Because ARIA-E can cause focal neurologic deficits that can mimic an ischemic stroke, treating clinicians should consider whether such symptoms could be due to ARIA-E before giving thrombolytic therapy in a patient being treated with LEQEMBI.

Caution should be exercised when considering the use of LEQEMBI in patients with factors that indicate an increased risk for ICH and, in particular, patients who need to be on anticoagulant therapy or patients with findings on MRI that are suggestive of CAA.

Radiographic Severity With LEQEMBI
Most ARIA-E radiographic events occurred within the first 7 doses, although ARIA can occur at any time, and patients can have >1 episode. Maximum radiographic severity of ARIA-E with LEQEMBI was mild in 4%, moderate in 7%, and severe in 1% of patients. Resolution on MRI occurred in 52% of ARIA-E patients by 12 weeks, 81% by 17 weeks, and 100% overall after detection. Maximum radiographic severity of ARIA-H microhemorrhage with LEQEMBI was mild in 9%, moderate in 2%, and severe in 3% of patients; superficial siderosis was mild in 4%, moderate in 1%, and severe in 0.4% of patients. With LEQEMBI, the rate of severe radiographic ARIA-E was highest in ApoE ε4 homozygotes (5%) vs heterozygotes (0.4%) or noncarriers (0%). With LEQEMBI, the rate of severe radiographic ARIA-H was highest in ApoE ε4 homozygotes (13.5%) vs heterozygotes (2.1%) or noncarriers (1.1%).

Monitoring and Dose Management Guidelines
Baseline brain MRI and periodic monitoring with MRI are recommended. Enhanced clinical vigilance for ARIA is recommended during the first 14 weeks of treatment. Depending on ARIA-E and ARIA-H clinical symptoms and radiographic severity, use clinical judgment when considering whether to continue dosing or to temporarily or permanently discontinue LEQEMBI. If a patient experiences ARIA symptoms, clinical evaluation should be performed, including MRI if indicated. If ARIA is observed on MRI, careful clinical evaluation should be performed prior to continuing treatment.

Hypersensitivity Reactions
Hypersensitivity reactions, including angioedema, bronchospasm, and anaphylaxis, have occurred with LEQEMBI. Promptly discontinue the infusion upon the first observation of any signs or symptoms consistent with a hypersensitivity reaction and initiate appropriate therapy.

Infusion-Related Reactions (IRRs)
IRRs were observed—LEQEMBI: 26%; placebo: 7%—and most cases with LEQEMBI (75%) occurred with the first infusion. IRRs were mostly mild (69%) or moderate (28%). Symptoms included fever and flu-like symptoms (chills, generalized aches, feeling shaky, and joint pain), nausea, vomiting, hypotension, hypertension, and oxygen desaturation.

IRRs can occur during or after the completion of infusion. In the event of an IRR during the infusion, the infusion rate may be reduced or discontinued, and appropriate therapy initiated as clinically indicated. Consider prophylactic treatment prior to future infusions with antihistamines, acetaminophen, nonsteroidal anti-inflammatory drugs, or corticosteroids.

ADVERSE REACTIONS

The most common adverse reactions reported in ≥5% with LEQEMBI infusion every 2 weeks and ≥2% higher than placebo were IRRs (LEQEMBI: 26%; placebo: 7%), ARIA-H (LEQEMBI: 14%; placebo: 8%), ARIA-E (LEQEMBI: 13%; placebo: 2%), headache (LEQEMBI: 11%; placebo: 8%), superficial siderosis of central nervous system (LEQEMBI: 6%; placebo: 3%), rash (LEQEMBI: 6%; placebo: 4%), and nausea/vomiting (LEQEMBI: 6%; placebo: 4%)Safety profile of LEQEMBI IQLIK for maintenance treatment was similar to LEQEMBI infusion. Patients who received LEQEMBI IQLIK experienced localized and systemic (less frequent) injection-related reactions (mild to moderate in severity) LEQEMBI (lecanemab-irmb) is available:

Intravenous infusion: 100 mg/mL Subcutaneous injection: 200 mg/mL Please see full Prescribing Information for LEQEMBI, including Boxed WARNING.

MEDIA CONTACTS Eisai Co., Ltd.
Public Relations Department
TEL: +81 (0)3-3817-5120
Biogen Inc.
Madeleine Shin
+1-781-464-3260
[email protected]
  Eisai Europe, Ltd.
EMEA Communications Department
+44 (0) 797 487 9419
[email protected]
   Eisai Inc. (U.S.)
Libby Holman
+1-201-753-1945
[email protected]
   INVESTOR CONTACTS   Eisai Co., Ltd.
Investor Relations Department
TEL: +81 (0) 3-3817-5122Biogen Inc.
Tim Power
+ 1-781-464-2442
[email protected]   Notes to Editors  1.About lecanemab (generic name, brand name: LEQEMBI®)
Lecanemab is the result of a strategic research alliance between Eisai and BioArctic. It is a humanized immunoglobulin gamma (IgG1) monoclonal antibody directed against aggregated soluble (protofibril) and insoluble forms of amyloid-beta (Aβ).Lecanemab has been approved in 51 countries and regions including Japan, the United States, Europe, China, South Korea, Taiwan, and Saudi Arabia, and is under regulatory review in 9 countries. Following the initial phase with treatment every two weeks for 18 months, intravenous (IV) maintenance dosing with treatment every four weeks was approved in the U.S., China, he United Kingdom, and others, and applications have been filed in 4 countries and regions. The U.S. FDA approved Eisai’s Biologics License Application (BLA) for subcutaneous maintenance dosing with LEQEMBI IQLIK in August 2025.

Since July 2020 the Phase 3 clinical study (AHEAD 3-45) for individuals with preclinical AD, meaning they are clinically normal and have intermediate or elevated levels of amyloid in their brains, is ongoing. AHEAD 3-45 is conducted as a public-private partnership between the Alzheimer's Clinical Trial Consortium that provides the infrastructure for academic clinical trials in AD and related dementias in the U.S, funded by the National Institute on Aging, part of the National Institutes of Health, Eisai and Biogen. Since January 2022, the Tau NexGen clinical study for Dominantly Inherited AD (DIAD), that is conducted by Dominantly Inherited Alzheimer Network Trials Unit (DIAN-TU), led by Washington University School of Medicine in St. Louis, is ongoing and includes lecanemab as the backbone anti-amyloid therapy.

  2.About the Collaboration between Eisai and Biogen for AD
Eisai and Biogen have been collaborating on the joint development and commercialization of AD treatments since 2014. Eisai serves as the lead of lecanemab development and regulatory submissions globally with both companies co-commercializing and co-promoting the product and Eisai having final decision-making authority.  3.About the Collaboration between Eisai and BioArctic for AD
Since 2005, Eisai and BioArctic have had a long-term collaboration regarding the development and commercialization of AD treatments. Eisai obtained the global rights to study, develop, manufacture and market lecanemab for the treatment of AD pursuant to an agreement with BioArctic in December 2007. The development and commercialization agreement on the antibody lecanemab back-up was signed in May 2015.  4.About Eisai Co., Ltd.
Eisai's Corporate Concept is "to give first thought to patients and people in the daily living domain, and to increase the benefits that health care provides." Under this Concept (also known ashuman health care(hhc) Concept), we aim to effectively achieve social good in the form of relieving anxiety over health and reducing health disparities. With a global network of R&D facilities, manufacturing sites and marketing subsidiaries, we strive to create and deliver innovative products to target diseases with high unmet medical needs, with a particular focus in our strategic areas of Neurology and Oncology.In addition, we demonstrate our commitment to the elimination of neglected tropical diseases (NTDs), which is a target (3.3) of the United Nations Sustainable Development Goals (SDGs), by working on various activities together with global partners.

For more information about Eisai, please visit www.eisai.com (for global headquarters: Eisai Co., Ltd.), and connect with us on X, LinkedIn and Facebook. The website and social media channels are intended for audiences outside of the UK and Europe. For audiences based in the UK and Europe, please visit www.eisai.eu and Eisai EMEA LinkedIn.

  5.About Biogen
Founded in 1978, Biogen is a leading biotechnology company that pioneers innovative science to deliver new medicines to transform patient’s lives and to create value for shareholders and our communities. We apply deep understanding of human biology and leverage different modalities to advance first-in-class treatments or therapies that deliver superior outcomes. Our approach is to take bold risks, balanced with return on investment to deliver long-term growth.The company routinely posts information that may be important to investors on its website at www.biogen.com. Follow Biogen on social media – Facebook, LinkedIn, X, YouTube.

Biogen Safe Harbor

This news release contains forward-looking statements, including about the potential clinical effects of lecanemab; the potential benefits, safety and efficacy of lecanemab; potential regulatory discussions, submissions and approvals and the timing thereof including for lecanemab-irmb (LEQEMBI IQLIK); the potential to streamline the Alzheimer's disease treatment pathway; the anticipated benefits and potential of Biogen's collaboration arrangements with Eisai; the potential of Biogen's commercial business and pipeline programs, including lecanemab; and risks and uncertainties associated with drug development and commercialization. These forward-looking statements may be accompanied by such words as “aim,” “anticipate,” “assume,” “believe,” “contemplate,” “continue,” “could,” “estimate,” “expect,” “forecast,” “goal,” “guidance,” “hope,” “intend,” “may,” “objective,” “outlook,” “plan,” “possible,” “potential,” “predict,” “project,” “prospect,” “should,” “target,” “will,” “would” or the negative of these words or other words and terms of similar meaning. Drug development and commercialization involve a high degree of risk, and only a small number of research and development programs result in commercialization of a product. Results in early-stage clinical trials may not be indicative of full results or results from later stage or larger scale clinical trials and do not ensure regulatory approval. You should not place undue reliance on these statements. Given their forward-looking nature, these statements involve substantial risks and uncertainties that may be based on inaccurate assumptions and could cause actual results to differ materially from those reflected in such statements.

These forward-looking statements are based on management’s current beliefs and assumptions and on information currently available to management. Given their nature, we cannot assure that any outcome expressed in these forward-looking statements will be realized in whole or in part. We caution that these statements are subject to risks and uncertainties, many of which are outside of our control and could cause future events or results to differ materially from those stated or implied in this document, including, among others, uncertainty of our long-term success in developing, licensing, or acquiring other product candidates or additional indications for existing products; expectations, plans, prospects and timing of actions relating to product approvals, approvals of additional indications for our existing products, sales, pricing, growth, reimbursement and launch of our marketed and pipeline products; the potential impact of increased product competition in the biopharmaceutical and healthcare industry, as well as any other markets in which we compete, including increased competition from new originator therapies, generics, prodrugs and biosimilars of existing products and products approved under abbreviated regulatory pathways; our ability to effectively implement our corporate strategy; difficulties in obtaining and maintaining adequate coverage, pricing, and reimbursement for our products; the drivers for growing our business, including our dependence on collaborators and other third parties for the development, regulatory approval, and commercialization of products and other aspects of our business, which are outside of our full control; risks related to commercialization of biosimilars, which is subject to such risks related to our reliance on third-parties, intellectual property, competitive and market challenges and regulatory compliance; the risk that positive results in a clinical trial may not be replicated in subsequent or confirmatory trials or success in early stage clinical trials may not be predictive of results in later stage or large scale clinical trials or trials in other potential indications; risks associated with clinical trials, including our ability to adequately manage clinical activities, unexpected concerns that may arise from additional data or analysis obtained during clinical trials, regulatory authorities may require additional information or further studies, or may fail to approve or may delay approval of our drug candidates; and the occurrence of adverse safety events, restrictions on use with our products, or product liability claims; and any other risks and uncertainties that are described in other reports we have filed with the U.S. Securities and Exchange Commission, which are available on the SEC’s website at www.sec.gov.

These statements speak only as of the date of this press release and are based on information and estimates available to us at this time. Should known or unknown risks or uncertainties materialize or should underlying assumptions prove inaccurate, actual results could vary materially from past results and those anticipated, estimated or projected. Investors are cautioned not to put undue reliance on forward-looking statements. A further list and description of risks, uncertainties and other matters can be found in our Annual Report on Form 10-K for the fiscal year ended December 31, 2024, and in our subsequent reports on Form 10-Q. Except as required by law, we do not undertake any obligation to publicly update any forward-looking statements whether as a result of any new information, future events, changed circumstances or otherwise.

Digital Media Disclosure
From time to time, we have used, or expect in the future to use, our investor relations website (investors.biogen.com), the Biogen LinkedIn account (linkedin.com/company/biogen) and the Biogen X account (https://x.com/biogen) as a means of disclosing information to the public in a broad, non-exclusionary manner, including for purposes of the SEC’s Regulation Fair Disclosure (Reg FD). Accordingly, investors should monitor our investor relations website and these social media channels in addition to our press releases, SEC filings, public conference calls and websites, as the information posted on them could be material to investors.

   References

Amin L, Harris DA. Aβ receptors specifically recognize molecular features displayed by fibril ends and neurotoxic oligomers. Nat Commun. 2021;12:3451. doi:10.1038/s41467-021-23507-z.Ono K, Tsuji M. Protofibrils of Amyloid-β are Important Targets of a Disease-Modifying Approach for Alzheimer's Disease. Int J Mol Sci. 2020;21(3):952. doi: 10.3390/ijms21030952. PMID: 32023927; PMCID: PMC7037706.Hampel H, Hardy J, Blennow K, et al. The amyloid-β pathway in Alzheimer's disease. Mol Psychiatry. 2021;26(10):5481-5503.
2025-11-25 12:53 5mo ago
2025-11-25 07:30 5mo ago
BridgeBio to Participate in December Investor Conferences stocknewsapi
BBIO
November 25, 2025 07:30 ET

 | Source:

BridgeBio Pharma, Inc.

PALO ALTO, Calif., Nov. 25, 2025 (GLOBE NEWSWIRE) -- BridgeBio Pharma, Inc. (Nasdaq: BBIO) (“BridgeBio” or the “Company”), a new type of biopharmaceutical company focused on genetic diseases, today announced that members of its management team will participate in fireside chats at the following healthcare investor conferences:

Piper Sandler Healthcare Conference, New York, NY: Fireside Chat on Tuesday, December 2 at 10:30 am ESTEvercoreISI HealthCONx Conference, Miami, FL: Fireside Chat on Wednesday, December 3 at 3:00 pm EST To access the live webcast of BridgeBio’s presentations, please visit the “Events and Presentations” page within the Investors section of the BridgeBio website at https://investor.bridgebio.com. A replay of the webcasts will be available on the BridgeBio website for 90 days following the event.

About BridgeBio Pharma, Inc.
BridgeBio Pharma, Inc. (BridgeBio; Nasdaq: BBIO) is a new type of biopharmaceutical company founded to discover, create, test, and deliver transformative medicines to treat patients who suffer from genetic diseases. BridgeBio’s pipeline of development programs ranges from early science to advanced clinical trials. BridgeBio was founded in 2015 and its team of experienced drug discoverers, developers and innovators are committed to applying advances in genetic medicine to help patients as quickly as possible. For more information visit bridgebio.com and follow us on LinkedIn, X, Facebook, Instagram, and YouTube. 

BridgeBio Media Contact:
Bubba Murarka, Executive Vice President, Corporate Development
[email protected]  
(650)-789-8220

BridgeBio Investor Contact:
Chinmay Shukla, Senior Vice President, Strategic Finance
[email protected]
2025-11-25 12:53 5mo ago
2025-11-25 07:30 5mo ago
Anavex Life Sciences Reports Fiscal 2025 Fourth Quarter Financial Results and Provides Business Update stocknewsapi
AVXL
Company to host a webcast t oday at 8:30 a.m. Eastern Time
2025-11-25 12:53 5mo ago
2025-11-25 07:30 5mo ago
REMINDER -- QGold Initiates Preliminary Economic Assessment of its Recently Acquired Quartz Mountain Gold Project in Oregon from Alamos Gold stocknewsapi
QGLDF
TORONTO, Nov. 25, 2025 (GLOBE NEWSWIRE) -- Q-Gold Resources Ltd. (TSXV: QGR; OTCQB: QGLDF) ("QGold" or the "Company") is pleased to announce the signing of an agreement dated November 20, 2025 with leading engineering firm Kappes, Cassiday & Associates ("KCA") to initiate a preliminary economic assessment ("PEA") on its flagship Quartz Mountain Gold Project located in Oregon, USA.

"Today's engagement of Kappes Cassiday, combined with our recently completed NI 43-101 technical report, positions QGold to unlock significant shareholder value from this strategically located asset in a proven historic mining district of Oregon, USA," commented Peter Tagliamonte, President and CEO of QGold. "With our recently completed financing, we anticipate an exceptionally active period ahead as we advance the Quartz Mountain Gold Project through critical development milestones in 2025 and 2026."

Acquired from Alamos Gold in Q3 of this year, the Quartz Mountain Gold Project is a promising gold development project in southcentral Oregon (see figure 1). The initiation of the PEA follows the recently published mineral resource estimate (the "Mineral Resource Estimate") in a technical report dated effective September 26, 2025, for the Quartz Mountain Gold Project. The highlights of the Mineral Resource Estimate include:

An estimated 1,543,000 ounces of gold with a grade of 0.96 g/t and 2,049,000 ounces of silver with a grade of 1.27 g/t within 50,002,000 tonnes in the indicated mineral resource categoryAn additional 148,000 ounces of gold with a grade of 0.77 g/t and 135,000 ounces of silver with a grade of 0.70 g/t within 5,992,000 tonnes in the inferred mineral resource categoryThe Mineral Resource Estimate is amenable to conventional open-pit mining methods The PEA now underway will provide a comprehensive evaluation of the project's economic potential, including mining methods, processing options, capital and operating costs, and projected financial returns. KCA brings decades of experience in metallurgical engineering and mine development, making them an ideal partner for this critical phase of advancement.

"With KCA, QGold is positioned to capitalize on the project's strategic advantages," added Peter Tagliamonte. "These include its favorable location, established infrastructure, solid mineral resource base, and the designation of gold as a strategic asset in the USA within a strong gold market."

The results of the PEA are expected to be completed in the coming months and will serve as a foundation for future technical studies and permitting activities.

Figure 1: Quartz Mountain Gold Project Location Map

Qualified Persons

The scientific and technical information contained in this news release has been reviewed and approved by Fred Brown, P.Geo., an independent consultant of the Company, and Dr. Andreas Rompel, Pr.Sci.Nat., Vice President, Exploration and a director of QGold, each a "qualified person" within the meaning of National Instrument 43-101 – Standards of Disclosure for Mineral Projects.

About Q-Gold Resources Ltd.

Q-Gold Resources Ltd. (TSXV: QGR; OTCQB: QGLDF; Börse Frankfurt: QX9G) is a publicly traded North American-based mineral exploration and development company focused on advancing gold and silver projects in mining-friendly jurisdictions across North America. The Company is operated by seasoned resource professionals.

The Company's shares are listed on the TSX Venture Exchange under the symbol "QGR", the OTCQB® market in the United States under "QGLDF", and the Börse Frankfurt exchange under "QX9G".

QGold is committed to advancing its portfolio of gold and silver assets toward production, with its primary focus on its flagship Quartz Mountain Gold Project in Oregon (USA) and the Mine Centre Gold Project in Ontario (Canada). The Company focuses on resource expansion through systematic exploration, disciplined project development backed by rigorous technical work, and responsible environmental stewardship in mining-friendly jurisdictions with established infrastructure.

For Further Information, Contact:

Peter Tagliamonte
Chief Executive Officer
Email: [email protected]
Website: https://qgoldresources.com
Cell: +1 (416) 564-2880

Cautionary Notes

This press release contains "forward-looking information" within the meaning of applicable Canadian securities legislation. Forward-looking information includes, but is not limited to, statements with respect to the PEA, including its anticipated impact and timing of results, and the Company’s beliefs, plans, expectations or intentions for the Quartz Mountain Gold Project and Mine Centre Gold Project, including its plans to progress its portfolio of assets toward production. Generally, forward-looking information can be identified by the use of forward-looking terminology such as "plans", "expects" or "does not expect", "is expected", "budget", "scheduled", "estimates", "forecasts", "intends", "anticipates" or "does not anticipate", or "believes", or variations of such words and phrases or state that certain actions, events or results "may", "could", "would", "might" or "will be taken", "occur" or "be achieved". Forward-looking information is subject to known and unknown risks, uncertainties and other factors that may cause the actual results, level of activity, performance or achievements of the Company, as the case may be, to be materially different from those expressed or implied by such forward-looking information, including but not limited to: receipt of necessary approvals; general business, economic, competitive, political and social uncertainties; future mineral prices and market demand; accidents, labour disputes and shortages and other risks of the mining industry. Although the Company has attempted to identify important factors that could cause actual results to differ materially from those contained in forward-looking information, there may be other factors that cause results not to be as anticipated, estimated or intended. There can be no assurance that such information will prove to be accurate, as actual results and future events could differ materially from those anticipated in such statements. Accordingly, readers should not place undue reliance on forward-looking information. The Company does not undertake to update any forward-looking information, except in accordance with applicable securities laws.

NEITHER THE TSX VENTURE EXCHANGE NOR ITS REGULATION SERVICES PROVIDER (AS THAT TERM IS DEFINED IN THE POLICIES OF THE TSX VENTURE EXCHANGE) ACCEPTS RESPONSIBILITY FOR THE ADEQUACY OR ACCURACY OF THIS RELEASE.

A photo accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/41af6681-3da1-4332-9f77-121cb0634037
2025-11-25 12:53 5mo ago
2025-11-25 07:30 5mo ago
Jayud Global Logistics Assumes Controlling Interest in Longgang Cross-Border E-Commerce Center stocknewsapi
JYD
November 25, 2025 07:30 ET

 | Source:

Jayud Global Logistics Ltd

SHENZHEN, China, Nov. 25, 2025 (GLOBE NEWSWIRE) -- Jayud Global Logistics Limited (NASDAQ: JYD) ("Jayud" or the "Company"), a leading end-to-end supply chain solution provider based in Shenzhen, specializing in cross-border logistics, today announced that it has acquired a controlling 52% ownership stake in the Longgang Cross-Border E-Commerce Center (the "Center"), elevating its previous minority position to majority control. This transaction positions Jayud to lead the Center's operations and expansion as a key hub for cross-border e-commerce logistics in the Longgang District of Shenzhen.

The Longgang Cross-Border E-Commerce Center serves as a comprehensive facility integrating warehousing, customs clearance, freight forwarding, and digital supply chain management services, strategically located to capitalize on Shenzhen's role as a global trade gateway. Going forward, the Company will direct strategic initiatives, including technology upgrades for real-time tracking, enhanced bonded logistics capabilities, and partnerships for international expansion. This control aligns with Jayud's broader vision to consolidate its footprint in high-growth e-commerce zones, driving increased throughput and revenue synergies.

The Longgang Cross-Border E-Commerce Center achieved remarkable results in 2024, handling 13,978 full-size containers with a total export value of USD 4.6 billion, representing 83,000 tons of cargo and 270 million parcels processed throughout the year.

As of September 30, 2025, the Center has continued its robust momentum, processing 6,863 full-size containers with a cumulative export value of USD 2.45 billion, totaling 44,129 tons of goods and 46.91 million parcels. These figures highlight Longgang’s growing role as a leading hub in China’s cross-border e-commerce supply chain, supporting global trade connectivity and high-quality logistics development.

"Acquiring a controlling interest in the Longgang Cross-Border E-Commerce Center represents a pivotal step in consolidating our leadership in Shenzhen's vibrant logistics landscape. This move will enable us to accelerate and scale our operations to meet the surging demand for cross-border solutions," said Mr. Xiaogang Geng, Chairman and Chief Executive Officer of Jayud Global Logistics Limited.

According to the Shenzhen Municipal Government:

In 2024, Shenzhen’s cross-border e-commerce imports and exports reached 372 billion RMB, ranking first in China for the third consecutive year.The city is home to over 150,000 cross-border e-commerce export enterprises.Shenzhen has attracted 80% of the world’s top 20 cross-border e-commerce platforms to establish operations in the city. About Jayud Global Logistics Limited

Jayud Global Logistics Limited is one of the leading Shenzhen-based end-to-end supply chain solution providers in China, focusing on cross-border logistics services. The Company benefits from the unique geographical advantages of providing a high degree of support for ocean, air, and overland logistics. The Company has established a global operation nexus featuring logistic facilities throughout major transportation hubs in China and globally, with footprints in 12 provinces in Mainland China and 16 countries across six continents. Jayud offers a comprehensive range of cross-border supply chain solutions, including freight forwarding, supply chain management, and other value-added services. With its strong service capabilities and research and development capabilities in proprietary IT systems, the Company provides customized and efficient logistics solutions and develops long-standing customer relationships. For more information, please visit the Company’s website: https://ir.jayud.com.

Forward-Looking Statements

Certain statements in this announcement are forward-looking statements. These forward-looking statements involve known and unknown risks and uncertainties and are based on the Company’s current expectations and projections about future events that the Company believes may affect its financial condition, results of operations, business strategy, and financial needs, including the expectation that the Offering will be successfully completed. Investors can identify these forward-looking statements by words or phrases such as “may”, “will”, “expect”, “anticipate”, “aim”, “estimate”, “intend”, “plan”, “believe”, “is/are likely to”, “potential”, “continue” or other similar expressions. The Company undertakes no obligation to update or revise publicly any forward-looking statements to reflect subsequent occurring events or circumstances, or changes in its expectations, except as may be required by law. Although the Company believes that the expectations expressed in these forward-looking statements are reasonable, it cannot assure you that such expectations will turn out to be correct, and the Company cautions investors that actual results may differ materially from the anticipated results and encourages investors to review other factors that may affect its future results in the Company’s registration statement and other filings with the SEC.

For more information, please contact:

Jayud Global Logistics Limited
Investor Relations Department
Email: [email protected] 

Investor Relations Contact:
Matthew Abenante, IRC
President
Strategic Investor Relations, LLC
Tel: 347-947-2093

Email: [email protected]
2025-11-25 12:53 5mo ago
2025-11-25 07:30 5mo ago
reAlpha (Nasdaq: AIRE) Acquires Prevu to Expand Multi-State Footprint and Offer Its Integrated Realty and Mortgage Services in Additional States stocknewsapi
AIRE
DUBLIN, Ohio, Nov. 25, 2025 (GLOBE NEWSWIRE) -- reAlpha Tech Corp. (Nasdaq: AIRE) (“reAlpha” or the “Company”), an AI-powered real estate technology company, today announced the acquisition of Prevu Inc. (“Prevu”), a digital homebuying platform with real estate brokerage operations across 12 states and Washington, D.C. The acquisition expands reAlpha’s licensed real estate footprint into 11 new markets and represents a step-change in the Company’s multi-service expansion, unifying realty and mortgage capabilities to support a broader national footprint.

Founded and headquartered in New York, Prevu is a digital-first, rebate-oriented brokerage model with more than 1,000 completed transactions, a 5-star Google rating, and an established homebuyer lead flow. Its proprietary platform is designed to streamline transactions, enhance agent productivity, and deliver a more efficient and transparent consumer experience. Prevu’s technology aligns closely with the Company’s product vision and the Company believes Prevu is well-positioned to integrate with Claire and internal automation workflows, creating meaningful opportunities to further strengthen the unified homebuying platform.

“Prevu brings both additional market coverage, as well as enhanced operational capabilities that we expect to accelerate reAlpha’s long-term platform strategy,” said Mike Logozzo, Chief Executive Officer of reAlpha. “We believe that integrating its brokerage business with our current real estate operations will unlock our ability to operate at scale and deliver greater consistency and transparency across the homebuying journey.”

“Becoming part of the reAlpha team marks an exciting next chapter for Prevu,” said Thomas Kutzman, Chief Executive Officer of Prevu. “Our shared commitment to modernizing real estate through technology and operational excellence makes this a natural fit. We look forward to leveraging reAlpha’s AI-powered platform, mortgage and title services, and engineering resources to further scale our impact and deliver even greater value to homebuyers and the agents that serve them.”

The acquisition marks the start of a structured integration process to bring Prevu’s brokerage operations, technology, and team into reAlpha’s unified homebuying platform. Early integration planning is underway to ensure continuity and focus on alignment as the companies begin combining their realty capabilities.

About Prevu, Inc.

Prevu is a real estate technology company on a mission to empower homebuyers. The company’s digital platform and Smart Buyer™ rebate offers a homebuying experience intended to provide consumers with greater control, transparency and savings when purchasing a home. This online experience is designed to deliver a smarter, more efficient way for homebuyers to transact. Prevu currently operates in major metropolitan markets in California, Colorado, Connecticut, Florida, Maryland, Massachusetts, New Jersey, New York, Pennsylvania, Texas, Virginia, Washington, Washington, D.C. To learn more, visit www.prevu.com.

About reAlpha Tech Corp.

reAlpha Tech Corp. (Nasdaq: AIRE) is an AI-powered real estate technology company that aims to transform the multi-trillion-dollar U.S. real estate services market. reAlpha is developing an end-to-end platform that streamlines real estate transactions through integrated brokerage, mortgage, and title services. With a strategic, acquisition-driven growth model and proprietary AI infrastructure, reAlpha is building a vertically integrated ecosystem designed to deliver a simpler, smarter, and more affordable path to homeownership. For more information, visit www.realpha.com.

Forward-Looking Statements

The information in this press release includes “forward-looking statements.” Any statements other than statements of historical fact contained herein, including statements by reAlpha’s Chief Executive Officer, Mike Logozzo and Chief Executive Officer of Prevu, Thomas Kutzman or statements about the Prevu acquisition, the anticipated benefits of the Prevu acquisition, reAlpha’s ability to integrate Prevu into its business and scale its business following the acquisition of Prevu and reAlpha’s long-term platform strategy, are forward-looking statements. In some cases, you can identify forward-looking statements by terminology such as “may”, “should”, “could”, “might”, “plan”, “possible”, “project”, “strive”, “budget”, “forecast”, “expect”, “intend”, “will”, “estimate”, “anticipate”, “believe”, “predict”, “potential” or “continue”, or the negatives of these terms or variations of them or similar terminology. Factors that may cause actual results to differ materially from current expectations include, but are not limited to: reAlpha’s ability to integrate the business of Prevu into its existing business and the anticipated demand for Prevu’s services; reAlpha’s ability to enhance its operational efficiency, improve cross-functional coordination and support the reAlpha platform’s continued growth through the implementation of its new internal organizational structure; reAlpha’s ability to successfully enter new geographic markets; reAlpha’s ability to integrate the business of previously acquired companies into its existing business and the anticipated demand for such acquired companies’ services; reAlpha’s ability to scale its operational capabilities to expand into additional geographic markets and nationally; reAlpha’s ability to commercialize its developing AI-based technologies; reAlpha’s ability to pay contractual obligations; reAlpha’s liquidity, operating performance, cash flow and ability to secure future financing on favorable terms if needed; reAlpha’s limited operating history and that reAlpha has not yet fully developed its AI-based technologies; whether reAlpha’s technology and products will be accepted and adopted by its customers and intended users; the potential loss of key employees of reAlpha and of its subsidiaries; the outcome of certain outstanding legal proceedings against reAlpha and any legal proceedings that might be instituted against reAlpha; reAlpha’s ability to obtain, and maintain, the required licenses to operate in the U.S. states in which it, or its subsidiaries, operate in, or intend to operate in; reAlpha’s ability to successfully identify and acquire companies that are complementary to its business model; reAlpha’s ability to maintain and strengthen its brand and reputation; reAlpha’s ability to benefit from the implementation and use of its internal AI-powered assistants; reAlpha’s ability to regain compliance with the minimum bid price requirement under Nasdaq Listing Rule 5550(a)(2) during the additional compliance period; reAlpha’s ability to maintain compliance with applicable Nasdaq listing rules; any accidents or incidents involving cybersecurity breaches and incidents; the availability of rebates, which may be limited or restricted by state law; risks specific to AI-based technologies, including potential inaccuracies, bias, or regulatory restrictions; risks related to data privacy, including evolving laws and consumer expectations; reAlpha’s ability to accurately forecast demand for AI-based real estate-focused products; reAlpha’s ability to execute business objectives and growth strategies successfully or sustain reAlpha’s growth; changes in applicable laws or regulations, and the impact of the regulatory environment and complexities with compliance related to such environment; and other risks and uncertainties indicated in reAlpha’s SEC filings. Forward-looking statements are based on the opinions and estimates of management at the date the statements are made and are subject to a variety of risks and uncertainties and other factors that could cause actual events or results to differ materially from those anticipated in the forward-looking statements. Although reAlpha believes that the expectations reflected in the forward-looking statements are reasonable, there can be no assurance that such expectations will prove to be correct. reAlpha’s future results, level of activity, performance or achievements may differ materially from those contemplated, expressed or implied by the forward-looking statements, and there is no representation that the actual results achieved will be the same, in whole or in part, as those set out in the forward-looking statements. For more information about the factors that could cause such differences, please refer to reAlpha’s filings with the SEC. Readers are cautioned not to put undue reliance on forward-looking statements, and reAlpha does not undertake any obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as required by law.

Media Contact:

Cristol Rippe, Chief Marketing Officer

[email protected]

Investor Relations Contact:

Adele Carey, VP of Investor Relations

[email protected]
2025-11-25 12:53 5mo ago
2025-11-25 07:30 5mo ago
BrainsWay to Host Virtual Analyst & Investor Day to Discuss the Company's Growth Strategy and Deep TMS™ Treatment December 1, 2025 stocknewsapi
BWAY
November 25, 2025 07:30 ET

 | Source:

BrainsWay

BURLINGTON, Mass. and JERUSALEM, Nov. 25, 2025 (GLOBE NEWSWIRE) -- BrainsWay Ltd. (NASDAQ & TASE: BWAY) (“BrainsWay” or the “Company”), a global leader in advanced noninvasive brain stimulation technologies, today announced that it will host a virtual Analyst & Investor Day on Monday, December 1, 2025 at 10:00 AM ET, during which company management will highlight various aspects of BrainsWay’s growth strategy. The event will feature Owen Scott Muir, MD, DFAACAP (Co-Founder, Chief Medical Officer, Radial), who will discuss the significant unmet need for various conditions and his clinical experience utilizing Deep TMS™, and Michael Gershenzon, CEO of Stella MSO, a management services organization servicing more than 20 mental health clinics across the U.S. and Israel, who will discuss his experience working with BrainsWay on BrainsWay’s strategic minority-stake investment in Stella. To register, click here.

The event will provide an overview of BrainsWay’s patented breakthrough treatment, Deep TMS, and the potential impact of its accelerated protocol. Deep TMS is a clinically proven, noninvasive in-office brain stimulation treatment that uses magnetic fields to activate neural networks in the brain to improve symptoms of certain mental health and addiction conditions, including depression, obsessive-compulsive disorder, and smoking addiction.

A live question and answer session will follow the formal presentations.

About Owen Scott Muir, MD, DFAACAP
Owen Scott Muir, MD, DFAACAP, is a dual-board-certified child, adolescent, and adult psychiatrist and the Chief Medical Officer of Radial Health and Neurolief. He is a leading investigator in advanced neuromodulation, with work spanning deep-TMS (H-coil platforms), accelerated protocols, vocal, video, language, and oculomotor biomarkers, and multimodal precision psychiatry. Dr. Muir has served as principal or co-investigator on trials involving BrainsWay, Magnus, Ampa, Psyrin, Videra, iRxReminder, Mind Medicine, and other cutting-edge technologies. His clinical programs have pioneered real-world deployment of accelerated neuromodulation for adolescents and adults with severe depression, OCD, suicidality, and treatment-resistant conditions. He is also the author of The Frontier Psychiatrists newsletter (2.5m reads), TikTok (8m views/year), LinkedIn (1m impressions/year with 7.7.% engagement rate) and the popular press Inessential Pharmacology, and continues to publish on the integration of AI-augmented neurotherapeutics into routine care.

About BrainsWay
BrainsWay is a global leader in advanced noninvasive neurostimulation treatments for mental health disorders. The Company is boldly advancing neuroscience with its proprietary Deep Transcranial Magnetic Stimulation (Deep TMS™) platform technology to improve health and transform lives. BrainsWay is the first and only TMS company to obtain three FDA-cleared indications backed by pivotal clinical studies demonstrating clinically proven efficacy. Current indications include major depressive disorder (including reduction of anxiety symptoms, commonly referred to as anxious depression), obsessive-compulsive disorder, and smoking addiction. The Company is dedicated to leading through superior science and building on its unparalleled body of clinical evidence. Additional clinical trials of Deep TMS in various psychiatric, neurological, and addiction disorders are underway. Founded in 2003, with operations in the United States and Israel, BrainsWay is committed to increasing global awareness of and broad access to Deep TMS. For the latest news and information about BrainsWay, please visit www.brainsway.com.

Forward-Looking Statements
This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. Such statements may be preceded by the words “intends,” “may,” “will,” “plans,” “expects,” “anticipates,” “projects,” “predicts,” “estimates,” “aims,” “targets,” “believes,” “hopes,” “potential” or similar words, and also includes any financial guidance and projections contained herein. These forward-looking statements and their implications are based on the current expectations of the management of the Company only and are subject to a number of factors and uncertainties that could cause actual results to differ materially from those described in the forward-looking statements. In addition, historical results or conclusions from scientific research and clinical studies – especially preliminary data which remains subject to peer-review – do not guarantee that future results would suggest similar conclusions or that historical results referred to herein would be interpreted similarly in light of additional research or otherwise. The following factors, among others, could cause actual results to differ materially from those described in the forward-looking statements: the failure to realize anticipated synergies and other benefits of the proposed transaction; the failure of our investments in management services organizations and/or other clinic-related entities to produce profitable returns; inadequacy of financial resources to meet future capital requirements; changes in technology and market requirements; delays or obstacles in launching and/or successfully completing planned studies and clinical trials; failure to obtain approvals by regulatory agencies on the Company’s anticipated timeframe, or at all; inability to retain or attract key employees whose knowledge is essential to the development of Deep TMS products; unforeseen difficulties with Deep TMS products and processes, and/or inability to develop necessary enhancements; unexpected costs related to Deep TMS products; failure to obtain and maintain adequate protection of the Company’s intellectual property, including intellectual property licensed to the Company; the potential for product liability; changes in legislation and applicable rules and regulations; unfavorable market perception and acceptance of Deep TMS technology; inadequate or delays in reimbursement from third-party payers, including insurance companies and Medicare; inability to commercialize Deep TMS, including internationally, by the Company or through third-party distributors; product development by competitors; inability to timely develop and introduce new technologies, products and applications, which could cause the actual results or performance of the Company to differ materially from those contemplated in such forward-looking statements.

Any forward-looking statement in this press release speaks only as of the date of this press release. The Company undertakes no obligation to publicly update or review any forward-looking statement, whether as a result of new information, future developments or otherwise, except as may be required by any applicable securities laws. More detailed information about the risks and uncertainties affecting the Company is contained under the heading “Risk Factors” in the Company’s filings with the U.S. Securities and Exchange Commission.

Contacts:
BrainsWay:
Ido Marom
Chief Financial Officer
[email protected]

Investors:
Brian Ritchie
LifeSci Advisors
[email protected]
2025-11-25 12:53 5mo ago
2025-11-25 07:30 5mo ago
Fusion Fuel's BrightHy Solutions Expands Green Hydrogen Footprint in Southern Europe with Agreement to Deliver New Electrolyzer and Hydrogen Refueling Station Project stocknewsapi
HTOO
Dublin, Ireland, Nov. 25, 2025 (GLOBE NEWSWIRE) -- Fusion Fuel Green PLC (NASDAQ: HTOO) (“Fusion Fuel” or the “Company”), a leading provider of full-service energy engineering, advisory, and utility solutions, today announced that its subsidiary, Bright Hydrogen Solutions Ltd (“BrightHy Solutions”), a leading engineering and advisory company specialized in green hydrogen, has signed a definitive contract to be the engineering, installation and equipment provider for a green hydrogen project in southern Europe. This follows the Company’s September 2 press release, in which BrightHy Solutions announced it had been selected to negotiate this agreement.

The contract, valued at up to approximately €1.7 million, covers the delivery of an electrolyzer system and hydrogen refueling station for a large construction company, supporting the region’s commitment to clean mobility and renewable energy transition. The project will be carried out in close collaboration with certain strategic partners of BrightHy Solutions.

Engineering work for the project has already commenced, and production of key equipment is underway. Once complete, the facility is expected to support the expanding hydrogen ecosystem in the region.

The full plant is expected to be delivered, installed, and commissioned in 2026.

“This contract represents a significant step forward not only for BrightHy Solutions, but also for the rapid build-out of hydrogen infrastructure across southern Europe,” said Luis Galdo, BrightHy Solutions’ Chief Commercial Officer. “We are proud to support our client’s forward-looking strategy and to contribute to a more sustainable energy future.”

About Fusion Fuel Green PLC

Fusion Fuel Green PLC (NASDAQ: HTOO) is an emerging leader in the energy services sector, offering a comprehensive suite of energy supply, distribution, and engineering and advisory solutions through its Al Shola Al Modea Gas Distribution LLC (“Al Shola Gas”), BrightHy Solutions, and BioSteam Energy (Proprietary) Limited (“BioSteam Energy”) businesses. Al Shola Gas provides full-service industrial gas solutions, including the design, supply, and maintenance of liquefied petroleum gas (LPG) systems, as well as the transport and distribution of LPG to a broad range of customers across commercial, industrial, and residential sectors. BrightHy Solutions, the Company’s hydrogen solutions platform, delivers innovative engineering and advisory services enabling decarbonization across hard-to-abate industries. BioSteam Energy provides biomass-powered industrial steam solutions to clients.

About Bright Hydrogen Solutions Ltd

BrightHy Solutions, a subsidiary of Fusion Fuel Green PLC (NASDAQ: HTOO), seeks to lead the hydrogen through electrolysis solutions market. With its substantial industry experience, BrightHy Solutions views itself as a partner to clients through the entire hydrogen production value chain including plant design, tailored engineering solutions, equipment sourcing, engineering and implementation oversight. BrightHy Solutions has a strong and core focus on safety, reliability, and efficiency. Find out more at www.brighthy.com.

Forward-Looking Statements

This press release includes “forward-looking statements” within the meaning of Section 27A of the U.S. Securities Act of 1933, as amended, and Section 21E of the U.S. Securities Exchange Act of 1934, as amended, which statements involve substantial risks and uncertainties. Forward-looking statements generally relate to future events or the Company’s future financial or operating performance. In some cases, you can identify these statements because they contain words such as “may,” “will,” “believes,” “expects,” “anticipates,” “estimates,” “projects,” “intends,” “should,” “seeks,” “future,” “continue,” “plan,” “target,” “predict,” “potential,” or the negative of such terms, or other comparable terminology that concern the Company’s expectations, strategy, plans, or intentions. Forward-looking statements relating to expectations about future results or events are based upon information available to the Company as of today’s date and are not guarantees of the future performance of the Company, and actual results may vary materially from the results and expectations discussed. The Company’s expectations and beliefs regarding these matters may not materialize, and actual results in future periods are subject to risks and uncertainties that could cause actual results to differ materially from those projected, including, without limitation, the ability of the parties to obtain all necessary regulatory and other consents and approvals and to deliver all required products and services in connection with the contemplated project; the ability of the project to generate the expected free cash flows or net income necessary for the Company to generate the anticipated returns in connection with the contemplated project; macroeconomic risks relating to currency exchange rates, inflation rates, interest rates, or other potentially disruptive factors; and the risks and uncertainties described under Item 3. “Key Information – D. Risk Factors” and elsewhere in the Company’s Annual Report on Form 20-F filed with the U.S. Securities and Exchange Commission (the “SEC”) on May 9, 2025 (the “Annual Report”), and other filings with the SEC. Should any of these risks or uncertainties materialize, or should the underlying assumptions about the Company’s business and the commercial markets in which the Company operates prove incorrect, actual results may vary materially from those described as anticipated, estimated or expected in the Annual Report. All subsequent written and oral forward-looking statements concerning the Company or other matters and attributable to the Company or any person acting on its behalf are expressly qualified in their entirety by the cautionary statements above. The Company does not undertake any obligation to publicly update any of these forward-looking statements to reflect events or circumstances that may arise after the date hereof, except as required by law.

Investor Relations Contact
[email protected]
www.fusion-fuel.eu
2025-11-25 12:53 5mo ago
2025-11-25 07:30 5mo ago
Will Alphabet Hit $4 Trillion Before the End of the Year? stocknewsapi
GOOG GOOGL
Alphabet ( NASDAQ:GOOG )( NASDAQ:GOOGL ) has been on a rocket ride this year, and its market capitalization recently crossed $3.62 trillion, overtaking Microsoft ( NASDAQ:MSFT ) to claim the title of third largest company globally.
2025-11-25 12:53 5mo ago
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Ituran: Profitable, Growing, And Ready For Its Next Leap stocknewsapi
ITRN
Analyst’s Disclosure:I/we have no stock, option or similar derivative position in any of the companies mentioned, and no plans to initiate any such positions within the next 72 hours. I wrote this article myself, and it expresses my own opinions. I am not receiving compensation for it (other than from Seeking Alpha). I have no business relationship with any company whose stock is mentioned in this article.

Seeking Alpha's Disclosure: Past performance is no guarantee of future results. No recommendation or advice is being given as to whether any investment is suitable for a particular investor. Any views or opinions expressed above may not reflect those of Seeking Alpha as a whole. Seeking Alpha is not a licensed securities dealer, broker or US investment adviser or investment bank. Our analysts are third party authors that include both professional investors and individual investors who may not be licensed or certified by any institute or regulatory body.
2025-11-25 12:53 5mo ago
2025-11-25 07:31 5mo ago
STRF: Double Digit Yield, Tax Advantaged Fixed Income stocknewsapi
STRF
Analyst’s Disclosure:I/we have a beneficial long position in the shares of BTC-USD, FBTC, MSTR either through stock ownership, options, or other derivatives. I wrote this article myself, and it expresses my own opinions. I am not receiving compensation for it (other than from Seeking Alpha). I have no business relationship with any company whose stock is mentioned in this article.

Seeking Alpha's Disclosure: Past performance is no guarantee of future results. No recommendation or advice is being given as to whether any investment is suitable for a particular investor. Any views or opinions expressed above may not reflect those of Seeking Alpha as a whole. Seeking Alpha is not a licensed securities dealer, broker or US investment adviser or investment bank. Our analysts are third party authors that include both professional investors and individual investors who may not be licensed or certified by any institute or regulatory body.
2025-11-25 12:53 5mo ago
2025-11-25 07:32 5mo ago
Burlington Stores Raises Outlook as Consumers Flock to Off-Price Retailers stocknewsapi
BURL
Burlington Stores BURL -4.06%decrease; red down pointing triangle reported higher third-quarter sales and raised its full-year outlook in the latest sign that consumers are flocking to off-price retailers due to concerns about inflation and the economy.

The off-price apparel retailer reported net income of $105 million, or $1.63 a share, up from $91 million, or $1.40 a share, the year prior.

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Quality Dividends On Clearance: Secure +7% Yields Today stocknewsapi
MO WES
Analyst’s Disclosure:I/we have a beneficial long position in the shares of WES, MO either through stock ownership, options, or other derivatives. I wrote this article myself, and it expresses my own opinions. I am not receiving compensation for it (other than from Seeking Alpha). I have no business relationship with any company whose stock is mentioned in this article.

Beyond Saving, Philip Mause, and Hidden Opportunities, all are supporting contributors for High Dividend Opportunities. Any recommendation posted in this article is not indefinite. We closely monitor all of our positions. We issue Buy and Sell alerts on our recommendations, which are exclusive to our members.

Seeking Alpha's Disclosure: Past performance is no guarantee of future results. No recommendation or advice is being given as to whether any investment is suitable for a particular investor. Any views or opinions expressed above may not reflect those of Seeking Alpha as a whole. Seeking Alpha is not a licensed securities dealer, broker or US investment adviser or investment bank. Our analysts are third party authors that include both professional investors and individual investors who may not be licensed or certified by any institute or regulatory body.
2025-11-25 12:53 5mo ago
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Dick's Sporting Goods Raises Fiscal-Year Guidance. The Stock Falls Sharply. stocknewsapi
DKS
The sporting goods retailer has struggled to win over investors this year.
2025-11-25 12:53 5mo ago
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Fujifilm to Highlight Cutting-Edge Imaging Innovations at RSNA 2025 stocknewsapi
FUJIY
-

New diagnostic imaging solutions to increase operational efficiencies and optimize patient care

LEXINGTON, Mass.--(BUSINESS WIRE)--FUJIFILM Healthcare Americas Corporation, a leader in diagnostic and enterprise imaging solutions, will highlight its latest diagnostic imaging innovations in booth #3300 in South Hall at the Radiological Society of North America (RSNA) 2025 annual meeting, held November 30 to December 3 at McCormick Place in Chicago. These new imaging advances are built for today’s demanding clinical environments, delivering intelligent mobile bedside imaging, unique Deep Learning MRI applications, high resolution surgical guidance and fully automated radiographic room efficiency.

“Fujifilm’s mission is to deliver imaging systems that not only meet the performance demands of the most challenging procedures, but also streamline workflows, reduce dose, and elevate the patient and clinician experience,” said Shawn Etheridge, executive director, modality solutions marketing, FUJIFILM Healthcare Americas Corporation. “RSNA 2025 gives us the opportunity to engage directly with clinicians on how Fujifilm’s solutions are delivering on that promise.”

Among the new innovations to be demonstrated at the booth:

AI-powered MRI image quality and workflow enhancements: DLR Symmetry leverages deep learning reconstruction to optimize image quality while reducing scan times using partial Fourier techniques. Additionally, AutoPose with AI extends automatic slice selection to chest, cardiac, pelvis and lower extremities improving precision, accelerating workflow and promoting consistent, repeatable imaging across a broader range of exams.

FDR Go iQ Portable Digital Radiography System: Fujifilm’s latest intelligent DR portable built for busy radiology departments is equipped with an intuitive tube head touch display and convenient in-bin detector smart charging. An intelligent built-in 3D camera provides live positioning guidance and tube to bed angulation and auto sensing SID display. FDR Go iQ brings x-ray room image quality to bedside exams.

Persona C-HR Mobile Fluoroscopy C-Arm: 25 kW power, high-sensitivity detector, and 82 cm wide opening combines to deliver high-resolution imaging at low dose. Designed for demanding OR workflows, Persona C-HR offers 30 fps pulsed fluoroscopy, active cooling, dedicated surgeon’s console with high resolution 32”, 4k display and a secondary tech display and controls, for advanced vascular capabilities in a lightweight, surgeon-friendly design.

FDR Visionary Digital Radiography Suite: Fujifilm’s flagship, auto-positioning room now features a collimator-integrated camera for live visual positioning guidance and workflow acceleration. The system’s automation intelligence delivers impressive speed and repeatability for efficient, faster workflow and options for automated advanced applications including long length imaging at the chest stand and table, bone subtraction and tomosynthesis.

Attendees of RSNA 2025 will be able to talk directly with Fujifilm’s experts to learn how these technologies integrate into busy imaging departments, long-length imaging suites, OR environments, and portable/mobile use cases.

For more information about our presence at RSNA, click here, or follow us on LinkedIn and X for #RSNA25 updates throughout the event.

About Fujifilm

FUJIFILM Healthcare Americas Corporation is a comprehensive healthcare company that has an extensive range of technology and expertise in the detection, diagnosis, and treatment of diseases. Fujifilm’s innovative portfolio includes solutions spanning diagnostic imaging, enterprise imaging, endoscopic imaging, surgical imaging, and in-vitro diagnostics. The Non-Destructive Testing group delivers radiography solutions to ensure high accuracy inspection of transportation infrastructure, and assets within aerospace, and oil and gas industries.

The company is headquartered in Lexington, Massachusetts. For more information on healthcare offerings, please visit https://healthcaresolutions-us.fujifilm.com, and for NDT portfolio, please visit https://www.fujifilm.com/us/en/business/industrial-materials/non-destructive-testing.

FUJIFILM Holdings Corporation, headquartered in Tokyo, leverages its depth of knowledge and proprietary core technologies to deliver innovative products and services across the globe through the four key business segments of healthcare, electronics, business innovation, and imaging with over 70,000 employees. Guided and united by our Group Purpose of “giving our world more smiles,” we address social challenges and create a positive impact on society through our products, services, and business operations. Under its medium-term management plan, VISION2030, which ends in FY2030, we aspire to continue our evolution into a company that creates value and smiles for various stakeholders as a collection of global leading businesses and achieve a global revenue of 4 trillion yen. For more information, please visit: https://holdings.fujifilm.com/en.

More News From FUJIFILM Healthcare Americas Corporation

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2025-11-25 12:53 5mo ago
2025-11-25 07:45 5mo ago
Fujifilm to Demonstrate Advances in AI Utilization, Speed and Automation in Enterprise Imaging Workflows at RSNA 2025 stocknewsapi
FUJIY
LEXINGTON, Mass.--(BUSINESS WIRE)--FUJIFILM Healthcare Americas Corporation, a leading provider of enterprise imaging and informatics solutions, will showcase new innovations in its industry leading Synapse medical informatics portfolio at the 2025 Radiological Society of North America (RSNA) Conference & Annual Meeting held November 30 to December 3. The new innovations in booth #3300 include a comprehensive enterprise imaging and informatics solution designed to meet the demands of outpatient imaging centers, and updates to Fujifilm’s flagship Synapse Enterprise PACS.

“Our customers are some of the world’s largest health systems and outpatient practices, and Fujifilm is steadfast in its commitment to deliver new innovative enterprise imaging technology which aligns with the needs of our global provider partners,” said Bill Lacy, senior vice president, medical informatics global business, FUJIFILM Healthcare Americas Corporation. “At this year’s RSNA, we’re shining a light on the continuous expansion of our Synapse enterprise imaging portfolio, and we are extremely excited to demonstrate the next generation of our cloud first Synapse PACS with native advanced visualization and AI adoption from imaging analytics to AI driven workflow.”

Fujifilm’s new medical informatics solutions that will be showcased at booth #3300 include:

Synapse PACS: Attendees will have the opportunity to demo Fujifilm’s flagship PACS which now embeds artificial intelligence and 3D advanced visualization applications, bringing automated study assignments and prioritization along with 3D-enhanced image analyses directly within the reader’s workflow. Synapse PACS delivers cloud-enabled enterprise imaging experiences that are tailored to each specialty and workflow, including radiology, mammography, cardiology, pathology, and point-of-care ultrasound. The system also introduced Synapse Viewer eXtension: a native PACS application that’s centered on speed and delivers a consistent reading experience regardless of location.

"The new system is really powerful, even when compared to other vendors' PACS," states Ben Arnold, PACS System Engineer, OhioHealth.

Synapse One: Fujifilm’s new, comprehensive, tailor-made workflow solution designed for unique outpatient imaging needs. This all-inclusive enterprise imaging solution enables providers to address everything from patient engagement, self-scheduling of exams, RIS (Radiology Information System), PACS (Picture Archiving and Communication System), advanced 3D imaging, physician portals, and more, all within the Synapse platform in the secure Amazon Web Services (AWS) cloud.

Also at RSNA, Roger Yang, MD, FACR, president of University Radiology Group (URG), will present on how to optimize AI-driven mammography workflows in PACS featuring Fujifilm’s Synapse AI Orchestrator on Tuesday, December 2 from 3:00-3:20 pm CT in South Hall-Level 3 Innovation Theater Booth #3316.

Dr. Yang will present on how his radiology network, URG, uses Fujifilm’s Synapse AI Orchestrator to optimize mammography workflows within Fujifilm’s Synapse PACS. Additionally, Dr. Yang will discuss URG’s results, the current industry architecture for delivering various AI-driven mammography findings to the PACS workstation and share real world examples on how Fujifilm’s AI Orchestrator is revolutionizing that concept by providing a common user experience, regardless of the AI engines in use, to help streamline workflows and support accurate mammography interpretations. Media that is interested in attending the presentation are kindly asked to fill out this form.

If you are attending RSNA 2025 and would like to book a demo to learn more, click here.

About Fujifilm

FUJIFILM Healthcare Americas Corporation is a comprehensive healthcare company that has an extensive range of technology and expertise in the detection, diagnosis, and treatment of diseases. Fujifilm’s innovative portfolio includes solutions spanning diagnostic imaging, enterprise imaging, endoscopic imaging, surgical imaging, and in-vitro diagnostics. The Non-Destructive Testing group delivers radiography solutions to ensure high accuracy inspection of transportation infrastructure, and assets within aerospace, and oil and gas industries.

The company is headquartered in Lexington, Massachusetts. For more information on healthcare offerings, please visit healthcaresolutions-us.fujifilm.com, and for NDT portfolio, please visit https://www.fujifilm.com/us/en/business/industrial-materials/non-destructive-testing.

FUJIFILM Holdings Corporation, headquartered in Tokyo, leverages its depth of knowledge and proprietary core technologies to deliver innovative products and services across the globe through the four key business segments of healthcare, electronics, business innovation, and imaging with over 70,000 employees. Guided and united by our Group Purpose of “giving our world more smiles,” we address social challenges and create a positive impact on society through our products, services, and business operations. Under its medium-term management plan, VISION2030, which ends in FY2030, we aspire to continue our evolution into a company that creates value and smiles for various stakeholders as a collection of global leading businesses and achieve a global revenue of 4 trillion yen. For more information, please visit: https://holdings.fujifilm.com/en.
2025-11-25 12:53 5mo ago
2025-11-25 07:45 5mo ago
Lazard Bolsters Global Industrials Practice by Adding Three New Managing Directors stocknewsapi
LAZ
-

Bill Young Joins the Firm as a Managing Director and Head of Diversified Industrials

Jean Greene Rejoins the Firm as a Managing Director

Paolo Battaglia to Join the Firm as a Managing Director

NEW YORK--(BUSINESS WIRE)--Lazard, Inc. (NYSE: LAZ), the preeminent global financial advisory and asset management firm, announced today the appointments of Bill Young, Jean Greene, and Paolo Battaglia as Managing Directors in the firm’s Global Industrials Group, all based in New York. These appointments further strengthen Lazard’s market-leading global Industrials franchise, which advises clients across diversified industrials, building products, chemicals, paper & packaging, transportation & logistics, industrial technology, and aerospace & defense.

Bill Young will serve as Head of Diversified Industrials. Jean Greene returns to Lazard, previously spending two decades at the firm. She will continue as a Managing Director, focused on advising clients across the industrials sector. Paolo Battaglia will join the firm in December as a Managing Director in Industrials and will advise clients across the sector.

“Our Industrials Group is experiencing strong momentum, and the addition of Bill, Jean, and Paolo further enhances our ability to deliver the highest quality strategic advice to clients across the sector,” said Mark McMaster, Global Head of Mergers & Acquisitions and Industrials at Lazard. “Their complementary skills and relationships will be tremendous assets to our team.”

“I’m thrilled to be rejoining Lazard and working alongside this talented team once again. The firm’s revitalized culture—marked by greater collaboration, innovation, and collegiality—has created an exciting environment for delivering exceptional strategic advice,” said Jean Greene, Managing Director at Lazard. “With Lazard’s renewed growth trajectory and clear vision for the future, I look forward to leveraging my experience to help clients navigate complex opportunities and challenges, while contributing to the firm’s continued success.”

About Bill Young

Bill Young is a Managing Director and Head of Diversified Industrials at Lazard, advising on transactions across the diversified industrial, industrial technology, and aerospace & defense sectors. Prior to joining Lazard, Bill was Co-Head of the North American Industrials Group as well as Global Co-Head of Diversified and Advanced Industrials sector coverage at Bank of America. Previously, Bill had been at Credit Suisse as Global Head of Diversified Industrials and Aerospace & Defense, where he originated and executed strategic transactions for a wide range of corporate and financial sponsor clients. Prior to Credit Suisse, Bill spent time at Wasserstein Perella as well as Rothschild & Co. Bill holds an MBA from Columbia Business School, an MSc in Economic History from the University of Oxford, and a BA in Economics and Government from Cornell University.

About Jean Greene

Jean Greene is a Managing Director in Lazard’s Industrials Group with over 25 years of investment banking experience. She rejoined Lazard after serving as a Managing Director at Bank of America, following two decades at Lazard earlier in her career. Jean began her investment banking career at Smith Barney, focusing on oil and gas financing and advisory. She serves on the Board of Directors of Dress for Success and the Board of Trustees of Goodspeed Musicals. Jean holds an undergraduate degree in Economics and French from Wellesley College and an MBA in Finance and Accounting from the University of Chicago Booth School of Business.

About Paolo Battaglia

Paolo Battaglia will join Lazard as a Managing Director in the Industrials Group, most recently serving as a Managing Director at Goldman Sachs. He began his career in private equity real estate at Lehman Brothers. Paolo serves as a Board Member at Friends of Bocconi in New York and is an Associate Member at the Economic Club of New York. He holds an M.Sc. in Finance and an undergraduate degree in Business Administration and Law from Bocconi University, both awarded cum laude, and has studied at NYU Stern.

About Lazard

Founded in 1848, Lazard is the preeminent financial advisory and asset management firm, with operations in North and South America, Europe, the Middle East, Asia, and Australia. Lazard provides advice on mergers and acquisitions, capital markets and capital solutions, restructuring and liability management, geopolitics, and other strategic matters, as well as asset management and investment solutions to institutions, corporations, governments, partnerships, family offices, and high net worth individuals. Lazard is listed on the New York Stock Exchange as Lazard, Inc. under the ticker LAZ. For more information, please visit Lazard.com and follow Lazard on LinkedIn.

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2025-11-25 12:53 5mo ago
2025-11-25 07:45 5mo ago
Lunai Bioworks Secures First Licensing LOI Following Landmark Breakthrough Showing Complete Tumor Regression in Humanized Cancer Models stocknewsapi
LNAI
Following peer-reviewed publication and independent expert review of findings, the LOI advances Lunai's tumor-regressing immune-cell platform toward scalable therapies for aggressive cancers

, /PRNewswire/ -- Lunai Bioworks (NASDAQ: LNAI), an AI-powered drug discovery and biodefense company, today announced it has secured its first Letter of Intent (LOI) to license its next-generation immune cell therapy, which achieved complete regression of both primary and metastatic pancreatic tumors with no recurrence in humanized preclinical models.

Images of control and 2nd Gen treatment condition mice using in vivo imaging system. Live imaging system was utilized to capture the tumor growth at various timepoints. The DC treated mouse showed absent signals of tumor at 5-week post dosing.

This milestone follows Lunai's recent peer-reviewed publication in Vaccines, a successful pre-IND meeting with the U.S. Food and Drug Administration (FDA), and growing third-party recognition from the biotechnology and scientific communities. Lunai has proposed a Phase I clinical trial evaluating its Dendritic Cell Combination Therapy (DCCT) across several high-need solid tumors, including pancreatic cancer, which currently has a five-year survival rate of just 13 percent.

"We are seeing accelerating validation from both researchers and industry partners," said David Weinstein, CEO of Lunai Bioworks. "Independent expert analysis confirms the strength of our data, while early licensing activity reflects growing confidence in this platform's potential to unlock scalable, off-the-shelf treatments capable of reaching the patients who need them most."

In a widely circulated post on LinkedIn, Benjamin McLeod, Founder of Convey Bio and Co-Host of Bio2Bedside, highlighted the study as a potential breakthrough in cancer immunotherapy.

In humanized mouse models of pancreatic cancer—one of the most lethal and treatment-resistant tumors—Lunai's DCCT achieved complete regression of both primary and metastatic lesions with no recurrence. These results demonstrate potent, multi-pathway immune activation.

Additionally, the late Dr. Anahid Jewett, Professor at UCLA and a leading authority in tumor immunology commented: "In our view, these results approach what could be called the 'holy grail' of cancer research. We observed an 80–90 percent reduction in tumor size and volume across two independent studies, with most of the remaining tissue consisting of immune cells rather than cancer cells."

Lunai is also advancing additional studies and expanding clinical reach for its DCCT platform through collaborations with leading investigators, including Dr. Steven Dubinett (UCLA) for non-small cell lung cancer and Dr. Xiaolin Zi (UC Irvine) for prostate cancer.

"Lunai's dendritic cell approach has the potential to overcome longstanding barriers in solid tumor treatment," said Dr. Dubinett, Dean of the David Geffen School of Medicine at UCLA.

Lunai's DCCT introduces a first-in-class, allogeneic immunotherapy designed to scale:

Lunai's DCCT leverages the natural antigen-presenting power of dendritic cells while eliminating the cost, time, and variability associated with patient-specific manufacturing.
The DCCT is manufactured from healthy donor cells and stored ready-to-use. This off-the-shelf model reduces manufacturing timelines from weeks to days, lowering the overall treatment cost.
In humanized mouse models of pancreatic cancer, one of the most lethal and treatment-resistant tumors, DCCT achieved complete regression of both primary and metastatic lesions with no recurrence.
Lunai Bioworks is preparing for formal licensing negotiations and pre-IND activities in early 2026, advancing toward clinical development of its dendritic cell therapy platform.

About Lunai Bioworks
Lunai Bioworks Inc. is an AI-powered drug discovery and biodefense company pioneering safe and responsible generative biology. With proprietary neurotoxicity datasets, advanced machine learning, and a focus on dual-use risk management, Lunai is redefining how artificial intelligence can accelerate therapeutic innovation while safeguarding society from emerging threats. For more, visit https://lunaibioworks.com.

SOURCE Lunai Bioworks Inc.
2025-11-25 12:53 5mo ago
2025-11-25 07:45 5mo ago
Jacobs to Manage Infrastructure Development Program to Support Regional Growth in El Paso, Texas stocknewsapi
J
Advancing water systems to support economic growth and resiliency

, /PRNewswire/ -- Jacobs (NYSE: J) has been selected by El Paso Water to provide program management and owner's representative services for its Utility Infrastructure Development Program near El Paso International Airport and Fort Bliss, one of the largest military installations in the U.S.

Jacobs will lead program planning and delivery of water, wastewater and stormwater infrastructure improvements to serve new development on approximately 4500 acres of land to meet growing demand in the City of El Paso. The multi-phase initiative will upgrade water, wastewater, and stormwater systems and is projected to cost approximately $200 million.

Jacobs Executive Vice President Eva Wood said: "This program is a catalyst for regional growth. Together with El Paso Water, we're powering the city's future, creating jobs, expanding critical infrastructure and building resilient and sustainable systems that will serve the community for generations."

El Paso Water Vice President of Operations and Technical Services Gilbert Trejo said: "We have confidence Jacobs can help us deliver the needed infrastructure to expand and improve water and wastewater services. Their expertise and proven track record make them a trusted partner in achieving our community's long-term sustainability goals."

While supporting regional growth, the upgrades will also enhance water reliability and wastewater capacity and support local workforce development.

Ranked No. 1 in Sewer & Waste and No. 2 in Program Management by Engineering News-Record, Jacobs delivers today's most complex, challenging and iconic infrastructure and transformation programs. Jacobs has supported programs like southern California's Pure Water Project Las Virgenes-Triunfo, which is securing a more resilient drinking water supply in the region, the Thames Tideway Tunnel, one of the largest water infrastructure projects ever undertaken in the U.K., and Central Interceptor, New Zealand's largest-ever wastewater project.  

At Jacobs, we're challenging today to reinvent tomorrow – delivering outcomes and solutions for the world's most complex challenges. With approximately $12 billion in annual revenue and a team of almost 45,000, we provide end-to-end services in advanced manufacturing, cities & places, energy, environmental, life sciences, transportation and water. From advisory and consulting, feasibility, planning, design, program and lifecycle management, we're creating a more connected and sustainable world. See how at jacobs.com and connect with us on LinkedIn, Instagram, X and Facebook.  

Certain statements contained in this press release constitute forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements are statements that do not directly relate to any historical or current fact. When used herein, words such as "expects," "anticipates," "believes," "seeks," "estimates," "plans," "intends," "future," "will," "would," "could," "can," "may," and similar words are intended to identify forward-looking statements. We base these forward-looking statements on management's current estimates and expectations, as well as currently available competitive, financial and economic data. Forward-looking statements, however, are inherently uncertain. There are a variety of factors that could cause business results to differ materially from our forward-looking statements including, but not limited to, uncertainties as to, the timing of the award of projects and funding and potential changes to the amounts provided for under the Infrastructure Investment and Jobs Act and other legislation and executive orders related to governmental spending, including any directive to federal agencies to reduce federal spending or the size of the federal workforce, and changes in U.S. or foreign tax laws, including the new tax legislation enacted in the U.S. in July 2025, statutes, rules, regulations or ordinances, including the impact of, and changes to tariffs and retaliatory tariffs or trade policies, that may adversely impact our future financial positions or results of operations, as well as general economic conditions, including inflation and the actions taken by monetary authorities in response to inflation, changes in interest rates and foreign currency exchange rates, changes in capital markets, the possibility of a recession or economic downturn, and increased uncertainty and risks, including policy risks and potential civil unrest, relating to the outcome of elections across our key markets and elevated geopolitical tension and conflicts, among others. For a description of these and additional factors that may occur that could cause actual results to differ from our forward-looking statements, see our filings with the U.S. Securities and Exchange Commission. The company is not under any duty to update any of the forward-looking statements after the date of this press release to conform to actual results, except as required by applicable law.

For press/media inquiries:
[email protected]  

SOURCE Jacobs
2025-11-25 12:53 5mo ago
2025-11-25 07:45 5mo ago
5 on board American Airlines flight hospitalized after odor diverts plane stocknewsapi
AAL
Five people on board an American Airlines flight were hospitalized after the plane was diverted due to an odor inside the flight deck and cabin, reports said.

The Federal Aviation Administration (FAA) said, "American Airlines Flight 2118 landed safely at George Bush Intercontinental Airport in Houston around 7:10 p.m. local time on Sunday, Nov. 23, after the crew reported fumes in the flight deck and cabin." 

"The Airbus A321 departed Orlando International Airport and was headed to Phoenix Sky Harbor International Airport," the FAA added. 

Four crew members and one passenger were taken to a hospital for treatment, FOX 4 News Dallas-Fort Worth reported, citing the Houston Fire Department. 

AMERICAN AIRLINES JET RETURNS TO LOS ANGELES AFTER PASSENGERS REPORT SICKENING FUMES 

An American Airlines Airbus A321 airplane taxis at Los Angeles International Airport on Oct. 17, 2025. (Kevin Carter/Getty Images / Getty Images)

It was not immediately clear what the odor was. 

"I'm gonna have some transports here out of the airport on this," a crew member was heard saying as the plane was diverted to Texas, according to KHOU. "Aircraft alert. I'm gonna need probably 4 transport units." 

Ticker Security Last Change Change % AAL AMERICAN AIRLINES GROUP INC. 13.10 +0.23
+1.79%
The other passengers on board the plane were then moved to a different aircraft to continue to Phoenix. 

"On Nov. 23, American Airlines Flight 2118 landed safely and taxied to the gate under its own power at Houston (IAH) following reports of an odor on board. The flight re-departed on a replacement aircraft," American Airlines said in a statement Tuesday to FOX Business. "We thank our team members for their professionalism and apologize to our customers for their experience."

TRUMP AXES BIDEN PLAN THAT WOULD HAVE FORCED AIRLINES TO PAY PASSENGERS CASH FOR DELAYS 

An American Airlines Airbus A321 airplane departs Los Angeles International Airport en route to Orlando on March 30, 2025. (Kevin Carter/Getty Images / Getty Images)

The FAA did not immediately respond Tuesday to a request for further comment from FOX Business. 

In October, another American Airlines plane turned around shortly after taking off from Los Angeles International Airport (LAX) "due to reports of an odor in the cabin," the airline said. 

The pilots in that incident also reported to air traffic control that they smelled and tasted something that prompted them to put on oxygen masks in the cockpit, WABC-TV reported. 

An American Airlines passenger plane is parked at a gate at Ronald Reagan Washington National Airport on Aug. 24, 2025, in Arlington, Virginia. (Daniel Slim/AFP via Getty Images / Getty Images)

CLICK HERE TO READ MORE ON FOX BUSINESS      

The plane landed back at LAX safely, and seven passengers were evaluated, but no one was taken to a medical facility for further treatment, WABC reported. 

FOX Business’ Pilar Arias contributed to this report. 
2025-11-25 12:53 5mo ago
2025-11-25 07:48 5mo ago
Best Buy Raises Outlook As Consumers Shrug Off Tariff Costs stocknewsapi
BBY
Comparable sales rose 2.7%, boosted by computing, gaming and mobile phones. andrew kelly/ReutersBest Buy BBY -1.09%decrease; red down pointing triangle reported higher fiscal third-quarter sales and raised its full-year outlook as consumers continue to spend despite concerns that tariffs costs could diminish discretionary spending.

The technology retailer on Tuesday posted net income of $140 million, or 66 cents a share, down from $273 million, or $1.26 a share, the year before.

Copyright ©2025 Dow Jones & Company, Inc. All Rights Reserved. 87990cbe856818d5eddac44c7b1cdeb8
2025-11-25 11:53 5mo ago
2025-11-25 06:24 5mo ago
Is This the Best Value Stock to Buy While Markets Are Volatile? stocknewsapi
PFE
This big pharma stock should be even more appealing to investors amid market turbulence.

You may have noticed that the markets are exceptionally volatile at the moment. That's true whether we're talking about stocks, cryptocurrencies, or commodities.

During turbulent times, many investors run for the hills. Some sell everything and park their money in cash. Others, however, seek safe havens. For example, value stocks in sectors that tend to perform well during choppy market conditions could appeal to many investors.

That brings me to Pfizer (PFE +0.72%). Is this the best value stock to buy while markets are volatile?

Image source: Getty Images.

Pfizer's volatility-resistant qualities
I've already alluded to one aspect of Pfizer that makes it resilient to volatility. Healthcare stocks typically fare better than most during stormy market periods. There's a simple reason why this is true: people need many healthcare products and services, regardless of what's happening with the economy or the stock market. This translates to relatively steady revenue and profits for healthcare companies.

Just look at Pfizer's top-selling blockbuster drugs. What doctor is going to stop prescribing Eliquis for patients with blood clots because the stock market is choppy? Will patients with transthyretin-mediated amyloidosis (ATTR) quit taking Vyndamax due to market swings? Of course not.

Pfizer's dividend could also make the stock more attractive to investors during market turbulence. The big pharma company's forward dividend yield is a juicy 6.9%. Importantly, Pfizer is generating ample free cash flow to cover the dividend payments.

Perhaps the most compelling proof of Pfizer's volatility-resistant qualities is the stock's five-year monthly beta of only 0.43. The lower the beta value is, the less volatile the stock is compared to the overall market.

Is Pfizer really a value stock?
This might seem to be a silly question, but is Pfizer really a value stock? After all, its shares trade at a forward price-to-earnings (P/E) ratio of 8.3. That's lower than Pfizer's historical average and only a fraction of the healthcare sector's forward earnings multiple of 18.2. However, there are two potential objections to classifying Pfizer as a true value stock.

First, the company's future growth prospects are suspect. Pfizer faces a major patent cliff. Autoimmune disease drug Xeljanz and blood thinner Eliquis lose U.S. patent protection next year (although generic rivals to Eliquis won't enter the market until 2028). Breast cancer drug Ibrance and prostate cancer drug Xtandi lose patent exclusivity in 2027.

Today's Change

(

0.72

%) $

0.18

Current Price

$

25.22

Second, the company's significant debt clouds the picture somewhat. Valuation metrics based on enterprise value arguably provide a better barometer for Pfizer. The pharma stock isn't expensive based on its enterprise value-to-EBITDA ratio of 10.2, but it's not quite as cheap as the forward earnings multiple suggests.

Still, I view Pfizer as a value stock. And I don't think it's a value trap, either. The drugmaker has enough products in its lineup that don't face losses of exclusivity in the near future and several promising late-stage pipeline candidates that should largely offset the anticipated revenue declines due to its patent cliff.

In particular, Pfizer's acquisitions have put it in a stronger position to successfully navigate its wave of exclusivity losses. The company's latest acquisition is the buyout of Metsera for up to $10 billion (around $7 billion upfront, with the remainder contingent upon achieving specified clinical and regulatory milestones). This deal holds the potential to make Pfizer a major player in the lucrative obesity drug market.

The best value stock to buy during high market volatility?
But is Pfizer the best value stock to buy during high market volatility? I wouldn't necessarily go that far. There are other contenders – and, quite frankly, I haven't researched all of them.

That said, I think Pfizer is a good value stock to buy when markets are turbulent. I like the ultra-high-yield dividend. I also think the company's growth prospects are better than they might appear at first glance.
2025-11-25 11:53 5mo ago
2025-11-25 06:24 5mo ago
Novo Nordisk phase 2 trial with amycretin reports significant weight loss and HbA1c reduction in type 2 diabetes stocknewsapi
NVO
Amycretin showed statistically significant weight loss of up to 14.5% at 36 weeksAmycretin demonstrated statistically significant reductions in HbA1c with up to 89.1% achieving HbA1c levels below 7%Amycretin appeared to have a safe and well-tolerated profile consistent with incretin and amylin-based therapies Bagsværd, Denmark, 25 November 2025 – Novo Nordisk today announced positive headline results from a phase 2 clinical trial with amycretin in people with type 2 diabetes. This marks the first evaluation of amycretin in people with type 2 diabetes, further demonstrating Novo Nordisk’s commitment to advancing innovation in the treatment of type 2 diabetes. Amycretin is a unimolecular agonist of the glucagon-like peptide 1 (GLP-1) and amylin receptors, intended for once-weekly subcutaneous administration and once-daily oral administration.

The trial investigated the efficacy, safety and pharmacokinetics of once-weekly subcutaneous amycretin and once-daily oral amycretin compared to placebo in 448 people with type 2 diabetes inadequately controlled on metformin with or without an SGLT2 inhibitor as standard of care. Approximately 40% of all participants were using an SGLT2 inhibitor before initiating the trial. The trial was a combined multiple ascending dose study, investigating six subcutaneous doses from 0.4 mg to 40 mg administered weekly, and three daily oral doses of 6 mg, 25 mg and 50 mg, with a total treatment duration of up to 36 weeks.

When evaluating the effects of treatment, if all people adhered to treatment1 from a mean baseline HbA1c of 7.8%, once-weekly subcutaneous amycretin achieved dose-dependent reductions in HbA1c of up to -1.8% by week 36. The proportion of people achieving HbA1c <7% and ≤6.5% was up to 89.1% and 76.2% respectively.

From a mean baseline HbA1c of 8.0%, people treated with once-daily oral amycretin achieved dose-dependent improvements in HbA1c of up to -1.5% by week 36. The proportion of people achieving an HbA1c level of <7% and ≤6.5% with once-daily oral amycretin was 77.6% and 62.6% respectively.

By comparison, people treated with placebo achieved HbA1c improvement of -0.2% and -0.4% with subcutaneous and oral amycretin, respectively. The estimated improvements in HbA1c were all statistically significant versus placebo, confirming the primary endpoints of the trial.

From a mean baseline body weight of 99.2 kg, subcutaneous amycretin achieved statistically significant weight loss of up to -14.5% compared to -2.6% in people treated with placebo. People treated with the highest dose of subcutaneous amycretin were on the final maintenance dose for a duration of 4 weeks. Similarly, from a mean baseline body weight of 101.1 kg, people treated with oral amycretin also achieved statistically significant weight loss of up to -10.1% compared to -2.5% in people treated with placebo. For the higher doses of amycretin, irrespective of administration route, no weight loss plateau was observed at week 36.

In the trial, subcutaneous and oral amycretin appeared to have a safe and well-tolerated profile, consistent with other incretin and amylin-based therapies. The most common adverse events with amycretin were gastrointestinal, and the vast majority were mild to moderate in severity.

“We are very encouraged by the phase 2 data with amycretin in people with type 2 diabetes - the first time amycretin has been evaluated in this population. The data further validate the potential best-in-class profile of amycretin” said Martin Holst Lange, chief scientific officer and executive vice president of Research and Development at Novo Nordisk. “Amycretin is built on the complementary biology of GLP-1 and amylin, and we are looking forward to bringing amycretin into an extensive phase 3 development programme across multiple indications in 2026”.

Based on the results, Novo Nordisk is now planning to initiate a phase 3 development programme with amycretin for adults with type 2 diabetes in 2026.

About amycretin
Amycretin is a unimolecular, long-acting GLP-1 and amylin receptor agonist under development by Novo Nordisk to provide an efficacious and convenient treatment for adults with overweight or obesity and as a treatment for adults with type 2 diabetes. Amycretin is developed for oral and subcutaneous administration.

About the Phase 2 trial in T2D
This trial is an interventional, multinational, multi-centre, randomised, parallel, double-blind (within arms), placebo-controlled, dose-finding study. The phase 2 trial investigated the safety, efficacy and PK properties of once-weekly subcutaneous and once-daily oral amycretin in participants with type 2 diabetes inadequately controlled (HbA1c 7.0-10.0 %) on a stable dose of metformin with or without an SGLT2 inhibitor. In the trial, close to two-thirds of the participants were male across both routes of administration. The trial consisted of nine active treatment arms. Participants received increasing doses of once-weekly subcutaneous amycretin (0.4 mg, 1.5 mg, 5 mg, 10 mg, 20 mg, and 40 mg) in six groups, and oral amycretin (6 mg, 25 mg, and 50 mg) in three groups for up to 36 weeks. The primary objective is to determine and characterise the dose-response relationship of subcutaneous and oral amycretin on change in HbA1c from baseline to week 36 in participants with type 2 diabetes. Secondary endpoints included changes in body weight (%) from baseline to week 36.

About Novo Nordisk
Novo Nordisk is a leading global healthcare company, founded in 1923 and headquartered in Denmark. Our purpose is to drive change to defeat serious chronic diseases, built upon our heritage in diabetes. We do so by pioneering scientific breakthroughs, expanding access to our medicines, and working to prevent and ultimately cure disease. Novo Nordisk employs about 78,500 people in 80 countries and markets its products in around 170 countries. Novo Nordisk's B shares are listed on Nasdaq Copenhagen (Novo-B). Its ADRs are listed on the New York Stock Exchange (NVO). For more information, visit novonordisk.com, Facebook, Instagram, X, LinkedIn and YouTube.

Publication of inside information pursuant to Market Abuse Regulation, Article 17.

Contacts for further information:

Media: Ambre James-Brown
+45 3079 9289
[email protected] Skrbkova (US)
+1 609 917 0632
[email protected]: Jacob Martin Wiborg Rode
+45 3075 5956
[email protected] Meyer
+45 3079 6656
[email protected] Ung
+45 3077 6414
[email protected] Christoffer Sho Togo Tullin
+45 3079 1471
[email protected] Bruce
+45 3444 2613
[email protected] Taylor Pitter
+1 609 613 0568
[email protected] Company announcement No 38 / 2025

1I.e. if all people followed the planned dosing schedule for the full trial period without initiation of rescue medication

CA251125-amycretin
2025-11-25 11:53 5mo ago
2025-11-25 06:27 5mo ago
Nasdaq Index: Nvidia Weakness Weighs on US Stocks as AI Chip News Hits Sentiment stocknewsapi
NVDA
The setup feels heavier than a typical Tuesday. You’ve got headline pressure, valuation worries, and a market that hasn’t given tech much room for error over the past week. Buyers are showing interest on dips, but today they’ll need more convincing.

Is Google Stealing a Bit of Nvidia’s Spotlight?
The Information reports that Meta is exploring Google’s tensor processing units starting in 2027 and may rent TPUs from Google Cloud as early as next year. That’s not an immediate blow to Nvidia, but it’s a clear signal that major buyers are testing alternatives.

Traders know Nvidia still dominates GPU supply for AI systems, yet Google’s custom chip strategy is gaining traction, and today’s premarket reaction shows how quickly investors react to competitive threats.

Alphabet is up roughly 3% after Monday’s rally, while Broadcom — a design partner for Google’s TPUs — is adding another 2% after an 11% jump yesterday.

Is Sandisk’s S&P 500 Debut a Sign of Tech’s Growing Weight?
2025-11-25 11:53 5mo ago
2025-11-25 06:29 5mo ago
Wall Street Breakfast Podcast: Nvidia's Chip Reign Challenged stocknewsapi
AMD BBBY GOOG GOOGL META NVDA SPOT TBHC
Getty Images

Listen below or on the go via Apple Podcasts and Spotify

Nvidia (NVDA) stock drops after report of Meta considering multi-billion-dollar deal for Google AI chips. (00:25) Bed Bath & Beyond (BBBY) to acquire The Brand House Collective (THBC) in $26.8M deal. (01:20) Spotify (SPOT) plans to increase U.S. subscription charges in Q1 2026 - report. (02:31)

This is an abridged transcript.

Nvidia (NVDA) extends slide to drop 3% premarket on Tuesday after a report that Meta Platforms (META) is in talks to spend billions on Google’s (GOOGL) (GOOG) AI chips.

Meta is in discussions to use the Google chips — known as tensor processing units, or TPUs — in data centers in 2027, The Information reported. Meta may also rent chips from Google’s cloud division next year, the news outlet said.

An agreement would position TPUs as a viable alternative to Nvidia’s chips and create significant competition for both Nvidia and Advanced Micro Devices, potentially undermining their sales and pricing power.

Google parent Alphabet (GOOGL) was up 2.7%, adding to a recent surge amid optimism over the latest version of its Gemini AI model. Advanced Micro Devices (AMD) meanwhile, sank 2.4%.

Bed Bath & Beyond (BBBY) will acquire The Brand House Collective (TBHC) in a merger agreement. The equity value for TBHC is approximately $26.8 million, based on stock prices from November 21, 2025. This value includes TBHC stock already held by Bed Bath & Beyond.

Bed Bath & Beyond currently holds approximately 40% of TBHC’s outstanding shares.

The Brand House Collective shareholders will receive 0.1993 shares of Bed Bath & Beyond common stock for each TBHC share.

The merger combines Bed Bath & Beyond's iconic brands and digital scale with The Brand House Collective's proven merchant model and store conversion expertise. This strategy is validated by early store conversions, which have already delivered double-digit sales growth, confirming the potential to scale a high-conversion format across the fleet.

In connection with the merger agreement, Bed Bath & Beyond has already advanced $10 million to The Brand House Collective under an existing delayed draw term loan facility to accelerate inventory procurement and fund operations.

The merger agreement was unanimously approved by both companies' boards.

The combined company expects to save at least $20 million annually by eliminating duplicated functions and inefficiencies. These savings will fund growth initiatives and enhancements.

Upon closing, Amy Sullivan is expected to become Chief Executive Officer of the newly organized Beyond Retail Group, managing omni-channel retail for BBBY's brands, including Bed Bath & Beyond and others.

As part of the broader efficiency strategy, the company has identified more than 40 underperforming or non-strategic stores for closure in early 2026 to improve the bottom line and optimize inventory.

The merger is expected to finalize in Q1 2026, pending lender consent from Bank of America and shareholder approval from The Brand House Collective. Bed Bath & Beyond owns 40% of the shares, and it is already committed to voting in favor of the deal.

Spotify (SPOT) is expected to raise U.S. subscription prices in Q1 2026.

According to a Financial Times report that cites people familiar with the matter, this will mark the first hike in U.S. price increases since mid‑2024, the report added.

Other media reports suggest that the prices will go up by $1 per month to $10.99 per month and the revision takes effect next week.

Spotify did not immediately respond to Seeking Alpha's request for comment.

The Swedish streaming company said back in August that it would raise prices to 11.99 euros ($13.82) per month from 10.99 euros in markets including South Asia, the Middle East, Africa, Europe, Latin America, and the Asia-Pacific region.

What’s Trending on Seeking Alpha

Initial Q3 GDP estimate to be released right before Christmas

Fed study sees tariffs lowering inflation then boosting it

Sandisk to join S&P 500; UPWK, FIBK, HBI to be part of S&P SmallCap 600

Catalyst watch:

Shareholders of Hanesbrands (HBI) will vote on the proposed merger with Gildan Activewear (GIL).

Best Buy (BBY) will hold its earnings conference call and give its outlook for the holiday quarter. Suppliers Netgear (NTGR), Turtle Beach (TBCH), and Sonos (SONO) all generate more than 10% of their revenue from Best Buy and have a high correlation to it on earnings day.

Dell Technologies (DELL) will hold a highly anticipated earnings conference call. Options trading implies a 10% swing for shares following the earnings release. Intel (INTC) will be on watch, since it has traded in the same direction as Dell after its last eight earnings reports.

Dow, S&P and Nasdaq futures are in the red. Crude oil is down 0.5% at $58/barrel. Bitcoin is down 1.3% at $87,000. Gold is flat at $4,137.

The FTSE 100 is flat and the DAX is down 0.2%.

The biggest movers for the day premarket: Keysight Technologies (KEYS) +14% - Shares jumped after delivering fourth-quarter earnings and guidance well above expectations.

On today’s economic calendar:

8:30 am The delayed September Retail Sales report is expected to be released by the U.S. Census Bureau.

8:30 am The delayed September Producer Price Index

Editor's Note: This article covers one or more microcap stocks. Please be aware of the risks associated with these stocks.
2025-11-25 11:53 5mo ago
2025-11-25 06:30 5mo ago
Nokia announces delisting from Paris Stock Exchange stocknewsapi
NOK
November 25, 2025 06:30 ET

 | Source:

Nokia Oyj

Nokia Corporation
Stock Exchange Release
25 November 2025 at 13:30 EET

Nokia announces delisting from Paris Stock Exchange

Espoo, Finland — Following its announcement on 4 November 2025 regarding the resolution by the Board of Directors of Nokia Corporation (“Nokia”) to submit an application for the delisting of its shares (ISIN: FI0009000681) from the regulated market of Euronext Paris (the “Paris Delisting”), Nokia announces today that the Paris Delisting has been approved by the Board of Euronext Paris. It is currently anticipated that the Paris Delisting will take effect on 31 December 2025.

In April 2015, Nokia shares were listed on Euronext Paris in conjunction with the acquisition of Alcatel-Lucent to ensure trading continuity for shareholders in France. The decision to delist was made following a review of the trading volumes, costs and administrative requirements related to Nokia’s listing on Euronext Paris.

The Paris Delisting has been approved by the Board of Euronext Paris and will not have any impact on Nokia’s day-to-day operations in France, nor on Nokia’s listings on the official list of Nasdaq Helsinki or on the New York Stock Exchange, where the Nokia shares trade in the form of American Depositary Receipts.

A voluntary sales facility (the “Sales Facility”) will be put in place in accordance with Euronext Paris’ rules to allow shareholders to sell their Nokia shares listed on Euronext Paris and held through the facilities of Euroclear France (the “Nokia Euronext Shares”).

The holders of Nokia Euronext Shares will have the following options:

Not to participate in the voluntary Sales Facility and keep all of their Nokia Euronext Shares, which they will be able to trade on Euronext Paris until the delisting date (exclusive) and on Nasdaq Helsinki thereafter through the facilities of Euroclear Finland, subject to the terms applied by their financial intermediary and their custody arrangements; or To participate in the voluntary Sales Facility (described below) to sell all or part of their Nokia Euronext Shares, in accordance with the rules and regulations of Euronext Paris. For the avoidance of doubt, holders of Nokia Euronext Shares will be able to trade on Euronext Paris until 30 December 2025 (the last trading date prior to the Paris Delisting).

Procedure for the Voluntary Sales Facility
Shareholders who wish to sell all or part of their Nokia Euronext Shares through the voluntary Sales Facility should request that their financial intermediaries deliver their Nokia Euronext Shares to Société Générale, acting as the centralizing agent, from 2 December 2025 to 15 December 2025 (inclusive).

Nokia Euronext Shares delivered to Société Générale will be sold on Nasdaq Helsinki as of 2 January 2026 at the market price prevailing at the time of sale. For the avoidance of doubt, Nokia will not be a party to the sale of the Nokia Euronext Shares tendered in the Sales Facility, such facility being operated independently by Société Générale without Nokia’s involvement.

Société Générale will calculate the average sale price of the Nokia Euronext Shares sold through the Sales Facility during the sales period and transfer the proceeds of the sale to the participating shareholders once the corresponding funds are fully received.

Nokia will pay the fees for the centralization and the brokerage fees related to the sale of Nokia Euronext Shares delivered to Société Générale as part of the voluntary Sales Facility.

This voluntary Sales Facility procedure is also described in a Euronext notice to be published on 27 November 2025.

Please note that no guarantee can be given by Nokia or by Société Générale as to the price at which the Nokia Euronext Shares tendered pursuant to the voluntary Sales Facility will actually be sold. This process is being provided solely as an accommodation to holders of Nokia Euronext Shares.

Holders of Nokia Euronext Shares may decide not to participate in the voluntary Sales Facility or may decide not to take any action, in which case no guarantee can be given to them on the terms that will be applied by their financial intermediary after the Paris Delisting. Shareholders are invited to consult their own financial, tax, and legal advisors before making a decision whether to participate in this process or not.

The indicative calendar of the voluntary Sales Facility and the Paris Delisting is summarized in the table below (it being specified that Nokia reserves the right to amend this calendar):

EventDateEuronext notice regarding the Sales Facility27 November 2025Beginning of the voluntary Sales Facility period 2 December 2025End of the voluntary Sales Facility period 15 December 2025Last day of trading of Nokia’s shares on Euronext Paris30 December 2025Delisting of the Nokia shares from Euronext Paris31 December 2025Sale on Nasdaq Helsinki of the Nokia Euronext Shares tendered in the voluntary Sales FacilityBeginning on 2 January 2026Allocation of the net proceeds of the sale to the relevant financial institutionsAs soon as possible after the determination of the average sale price and the receipt of the funds Shareholders participating in the voluntary Sales Facility are reminded that they acknowledge and accept the risks related to the change in the share market price between the date on which their Nokia Euronext Shares are delivered to Société Générale for participation in the voluntary Sales Facility and the receipt of funds after the determination of the applicable average sale price. All tenders of Nokia Euronext Shares under the Sales Facility will be irrevocable.

Shareholders are invited to contact their financial intermediaries for further information regarding the procedures for participating in the Sales Facility.

Additional information will be available in a FAQ to be published on Nokia’s website.

About Nokia

Nokia is a global leader in connectivity for the AI era. With expertise across fixed, mobile, and transport networks, powered by the innovation of Nokia Bell Labs, we’re advancing connectivity to secure a brighter world.

Inquiries:

Nokia
Communications
Phone: +358 10 448 4900
Email: [email protected]
Maria Vaismaa, Vice President, Global Media Relations

Nokia
Investor Relations
Phone: +358 931 580 507
Email: [email protected]

FORWARD-LOOKING STATEMENTS 

Certain statements herein that are not historical facts are forward-looking statements. These forward-looking statements reflect Nokia's current expectations and views of future developments and include statements regarding: A) expectations, plans, benefits or outlook related to our strategies, projects, programs, product launches, growth management, licenses, sustainability and other ESG targets, operational key performance indicators and decisions on market exits; B) expectations, plans or benefits related to future performance of our businesses (including the expected impact, timing and duration of potential global pandemics, geopolitical conflicts and the general or regional macroeconomic conditions on our businesses, our supply chain, the timing of market changes or turning points in demand and our customers’ businesses) and any future dividends and other distributions of profit; C) expectations and targets regarding financial performance and results of operations, including market share, prices, net sales, income, margins, cash flows, cost savings, the timing of receivables, operating expenses, provisions, impairments, tariffs, taxes, currency exchange rates, hedging, investment funds, inflation, product cost reductions, competitiveness, value creation, revenue generation in any specific region, and licensing income and payments; D) ability to execute, expectations, plans or benefits related to transactions, investments and changes in organizational structure and operating model; E) impact on revenue with respect to litigation/renewal discussions; and F) any statements preceded by or including "anticipate", “continue”, “believe”, “envisage”, “expect”, “aim”, “will”, “target”, “may”, “would”, “could“, "see", “plan”, “ensure” or similar expressions. These forward-looking statements are subject to a number of risks and uncertainties, many of which are beyond our control, which could cause our actual results to differ materially from such statements. These statements are based on management’s best assumptions and beliefs in light of the information currently available to them. These forward-looking statements are only predictions based upon our current expectations and views of future events and developments and are subject to risks and uncertainties that are difficult to predict because they relate to events and depend on circumstances that will occur in the future. Factors, including risks and uncertainties that could cause these differences, include those risks and uncertainties identified in our 2024 annual report on Form 20-F published on 13 March 2025 under Operating and financial review and prospects-Risk factors.
2025-11-25 11:53 5mo ago
2025-11-25 06:30 5mo ago
AuMEGA Metals Expands Drill Program stocknewsapi
AUMMF
November 25, 2025 6:30 AM EST | Source: AuMEGA Metals Ltd.
Edmonton, Alberta--(Newsfile Corp. - November 25, 2025) - AuMEGA Metals Ltd (ASX: AAM) (TSXV: AUM) (OTCQB: AUMMF) ("AuMEGA" or "the Company") is pleased to announce that it has mobilised a second diamond drill rig to expand the diamond drilling program on the Major Electromagnetic ("EM") anomaly at the Cape Ray Gold Project in Newfoundland and Labrador, Canada (Figure 1).

The current diamond drill program is progressing well and is currently focused on a large, newly defined airborne electromagnetic ("EM") conductor located in the immediate hangingwall of the Central Zone — a proven high-grade gold system (Figure 2)1.

The conductor, measuring approximately 500 metres by 1,000 metres and open along strike, is located 500 metres southeast of the Company's high-grade Central Zone deposits, and yet has never been drill tested (Figure 2).

Figure 1: AuMEGA Metals Portfolio on the Cape Ray Shear Zone and Hermitage Flexure

To view an enhanced version of this graphic, please visit:
https://images.newsfilecorp.com/files/10713/275841_f5fdd9dbe414794c_001full.jpg

AuMEGA Metal's Managing Director and CEO, Sam Pazuki, commented:

"Our fully funded drill program is progressing well and we have made the decision to dispatch a second drill rig to support the drilling efforts. Our plan is to drill as much as we can for the next few weeks before the winter break. We are excited about drilling the first ever exploration holes into the hangingwall of the Cape Ray Shear Zone near Central Zone.

"Additionally, we have pending assay results from several exploration programs. These include Bunker Hill, Cape Ray, Isle aux Morts Granite and Hermitage surficial till geochemical surveys along with the associated mapping and sampling programs. The results from these programs are expected to generate several new drill-ready targets as we continue to systematically explore our district-scale land package to find the next series of major deposits."

This announcement has been authorised for release by the Company's Board of Directors.

To learn more about the Company, please visit www.aumegametals.com, or contact:

Sam Pazuki, Managing Director & CEO
Canada Phone: +1 780 665 4925
Australia Phone: +61 8 6117 0478
Email: [email protected]

About the Company

AuMEGA Metals Ltd (ASX: AAM) (TSXV: AUM) (OTCQB: AUMMF) is utilising best-in-class exploration to explore on its district scale land package that spans 110 kilometers along the Cape Ray Shear Zone, a significant under-explored geological feature recognised as Newfoundland, Canada's largest identified gold structure. This zone currently hosts Equinox Gold's Valentine Gold Project, a multi-million-ounce deposit which is the region's largest gold project, along with AuMEGA's expanding Mineral Resource.

The Company is supported by a diverse shareholder registry of prominent global institutional investors, and strategic investment from B2Gold Corp, a significant, intermediate gold producer.

Additionally, AuMEGA holds a 27-kilometre stretch of the highly prospective Hermitage Flexure and has also secured an Option Agreement for the Blue Cove Copper Project in southeastern Newfoundland, which exhibits strong potential for copper and other base metals.

AuMEGA's Cape Ray Shear Zone hosts several dozen high potential targets along with its existing defined gold Mineral Resource of 6.2 million tonnes grading an average of 2.25 g/t, totaling 450,000 ounces of Indicated Resources, and 3.4 million tonnes grading an average of 1.44 g/t, totaling 160,000 ounces in Inferred Resources2.

AuMEGA acknowledges the financial support of the Junior Exploration Assistance Program, Department of Industry, Energy and Technology, Provincial Government of Newfoundland and Labrador, Canada.

Reference to Previous Announcements

In relation to this news release, all data used to assess targets have been previously disclosed by the Company and referenced in previous JORC Table 1 releases. Please see announcements dated: 16 October 2025, 2 October 2025 and 30 May 2023 as well as Newfoundland and Labrador Mineral Assessment Report #011O/0326 submitted by Dolphin Exploration Ltd in 1988.

In relation to the Mineral Resource estimate announced on 30 May 2023, the Company confirms that all material assumptions and technical parameters underpinning the estimates in that announcement continue to apply and have not materially changed. The Company confirms that the form and context in which the Competent Person's findings are presented have not been materially modified from the original market announcement.

Competent Person's Statements

Geophysics

AuMEGA contracted Axiom Exploration Group Ltd. in conjunction with RPM Aerial Services and Breton Air to fly a TDEM survey using Axiom's proprietary 30Hz XciteTM TDEM system which collected both time domain electromagnetic and magnetic data simultaneously. Flight lines were spaced 100 metres apart at an orientation of 152-332° with tie lines spaced at 1000 metres at an orientation of 62-242°. The survey covered a total area of 59.5 square kilometres.

Historic Results

Some data disclosed in this news release is related to historical sampling. The company has not independently analyzed the results to verify the results; however, the Company considers these historical results relevant as the Company is using this data as a guide to plan exploration programs. The full results of the historical work referenced in this release can be accessed online.

Qualified Person

The scientific and technical information in this press release was reviewed and approved by Shamus Duff, P. Geo., Project Geologist. Mr. Duff is a Qualified Person as defined under National Instrument 43-101 and a Professional Geologist registered with Professional Engineers and Geoscientists of Newfoundland and Labrador (PEGNL). Mr. Duff consents to the publication of this press release and certifies that the information is provided fairly and accurately represents the scientific and technical information disclosed within it.

1 2 October 2025 & 30 May 2023 News Release
2 News release dated 30 May 2023

To view the source version of this press release, please visit https://www.newsfilecorp.com/release/275841
2025-11-25 11:53 5mo ago
2025-11-25 06:30 5mo ago
LyondellBasell to address 2025 Goldman Sachs Industrials and Materials Conference stocknewsapi
LYB
HOUSTON and LONDON, Nov. 25, 2025 (GLOBE NEWSWIRE) -- LyondellBasell (NYSE: LYB), a leader in the global chemical industry, today announced Agustin Izquierdo, executive vice president and chief financial officer, will participate in a fireside chat at the 2025 Goldman Sachs Industrials and Materials Conference in New York on Wednesday, December 3, 2025, at 9:20 a.m. EST.

Webcast and Presentation Slides Access
A live webcast can be accessed at the time of the event at https://investors.lyondellbasell.com/events-and-presentations/default.aspx. A replay of the event will be available at the same link within 24 hours following the webcast.

About LyondellBasell 
We are LyondellBasell (NYSE: LYB) – a leader in the global chemical industry creating solutions for everyday sustainable living. Through advanced technology and focused investments, we are enabling a circular and low carbon economy. Across all we do, we aim to unlock value for our customers, investors and society. As one of the world's largest producers of polymers and a leader in polyolefin technologies, we develop, manufacture and market high-quality and innovative products for applications ranging from sustainable transportation and food safety to clean water and quality healthcare. For more information, please visit www.lyondellbasell.com or follow @LyondellBasell on LinkedIn.
2025-11-25 11:53 5mo ago
2025-11-25 06:30 5mo ago
Andean Precious Metals Strengthens Balance Sheet with New $40 Million Credit Facility from National Bank of Canada stocknewsapi
ANPMF
November 25, 2025 6:30 AM EST | Source: Andean Precious Metals Corp.
Toronto, Ontario--(Newsfile Corp. - November 25, 2025) - Andean Precious Metals Corp. (TSX: APM) (OTCQX: ANPMF) ("Andean" or the "Company") is pleased to announce that it has entered into a new revolving credit facility with National Bank of Canada ("NBC"), further strengthening the Company's capital structure and enhancing financial flexibility.

NBC Revolving Credit Facility Key Terms:

Capacity: US$40 million, automatically reducing to US$30 million on the first anniversaryTerm: 2 yearsInterest rate: SOFR + 4.25%The new facility provides improved liquidity and a more efficient cost of capital as Andean advances its strategic and operational initiatives across its portfolio.

Closure of Existing Credit Facilities

Concurrent with the closing of the NBC Revolving Credit Facility, Andean has:

Extinguished and closed the CommerceWest Main Street Lending Program Loan, totaling US$36.1 million, which was fully repaid using a combination of drawdowns from the new NBC Revolving Credit Facility and cash on hand; and

Closed the Company's existing US$25 million credit facility with Banco Santander International, which has been retired in conjunction with the establishment of the NBC Revolving Credit Facility. With these actions, Andean has simplified its capital structure, reduced the number of outstanding credit facilities, and aligned its financing arrangements with the Company's current scale and growth plans.

Juan Carlos Sandoval, Chief Financial Officer, stated: "The new credit facility with National Bank of Canada represents a significant milestone in optimizing our balance sheet and reinforcing financial flexibility to support the Company's next stage of growth. By consolidating and retiring prior credit arrangements, we have streamlined our capital structure, enhanced liquidity, and secured a more competitive cost of capital. We value NBC's partnership and remain committed to strengthening our financial position as we advance our strategic objectives."

About Andean Precious Metals

Andean is a growing precious metals producer focused on expanding into top-tier jurisdictions in the Americas. The Company owns and operates the San Bartolome processing facility in Potosí, Bolivia and the Golden Queen mine in Kern County, California, and is well-funded to act on future growth opportunities. Andean's leadership team is committed to creating value; fostering safe, sustainable and responsible operations; and achieving our ambition to be a multi-asset, mid-tier precious metals producer.

Caution Regarding Forward-Looking Statements

Certain statements and information in this release constitute "forward-looking statements" within the meaning of applicable U.S. securities laws and "forward-looking information" within the meaning of applicable Canadian securities laws, which we refer to collectively as "forward-looking statements". Forward-looking statements are statements and information regarding possible events, conditions or results of operations that are based upon assumptions about future economic conditions and courses of action. All statements and information other than statements of historical fact may be forward-looking statements. In some cases, forward-looking statements can be identified by the use of words such as "seek", "expect", "anticipate", "budget", "plan", "estimate", "continue", "forecast", "intend", "believe", "predict", "potential", "target", "may", "could", "would", "might", "will" and similar words or phrases (including negative variations) suggesting future outcomes or statements regarding an outlook. Forward-looking statements in this release include, but are not limited to, statements and information regarding the anticipated effects of the NBC credit facility. Such forward-looking statements are based on a number of material factors and assumptions, including, but not limited to: the Company's ability to carry on exploration and development activities; the Company's ability to secure and to meet obligations under property and option agreements and other material agreements; the timely receipt of required approvals and permits; that there is no material adverse change affecting the Company or its properties; that contracted parties provide goods or services in a timely manner; that no unusual geological or technical problems occur; that plant and equipment function as anticipated and that there is no material adverse change in the price of silver, price of gold, costs associated with production or recovery. Forward-looking statements involve known and unknown risks, uncertainties and other factors which may cause actual results, performance or achievements, or industry results, to differ materially from those anticipated in such forward-looking statements. The Company believes the expectations reflected in such forward-looking statements are reasonable, but no assurance can be given that these expectations will prove to be correct, and you are cautioned not to place undue reliance on forward-looking statements contained herein. Some of the risks and other factors which could cause actual results to differ materially from those expressed in the forward-looking statements contained in this release include, but are not limited to: risks and uncertainties relating to the interpretation of drill results, the geology, grade and continuity of mineral deposits and conclusions of economic evaluations; results of initial feasibility, pre-feasibility and feasibility studies, and the possibility that future exploration, development or mining results will not be consistent with the Company's expectations; risks relating to possible variations in reserves, resources, grade, planned mining dilution and ore loss, or recovery rates and changes in project parameters as plans continue to be refined; mining and development risks, including risks related to accidents, equipment breakdowns, labour disputes (including work stoppages and strikes) or other unanticipated difficulties with or interruptions in exploration and development; the potential for delays in exploration or development activities or the completion of feasibility studies; risks related to the inherent uncertainty of production and cost estimates and the potential for unexpected costs and expenses; risks related to commodity price and foreign exchange rate fluctuations; the uncertainty of profitability based upon the cyclical nature of the industry in which the Company operates; risks related to failure to obtain adequate financing on a timely basis and on acceptable terms or delays in obtaining governmental or local community approvals or in the completion of development or construction activities; risks related to environmental regulation and liability; political and regulatory risks associated with mining and exploration; risks related to the uncertain global economic environment; and other factors contained in the section entitled "Risk Factors" in the Company's MD&A for the three and nine months ended September 30, 2025.

Although the Company has attempted to identify important factors that could cause actual results or events to differ materially from those described in the forward-looking statements, you are cautioned that this list is not exhaustive and there may be other factors that the Company has not identified. Furthermore, the Company undertakes no obligation to update or revise any forward-looking statements included in this release if these beliefs, estimates and opinions or other circumstances should change, except as otherwise required by applicable law.

To view the source version of this press release, please visit https://www.newsfilecorp.com/release/275854