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Wednesday, October 8, 2025

XTLB Phase II hCDR1 Milestone, Yeda Licensing Deal

  XTLB shares surged 22.81% after hCDR1 entered Phase II trials for autoimmune diseases, boosting investor confidence.

- A licensing deal with Yeda Research reduced R&D risks and validated XTLB's scientific foundation for hCDR1 development.

- Acquisition of an AI firm and CEO Noam Band's appointment signaled strategic shifts but raised questions about operational focus.

- Financial challenges persist with Nasdaq compliance issues and reliance on private funding, complicating long-term growth prospects.

Shares of

(XTLB) surged to their highest level since October 2025, with an intraday gain of 37.72% before settling at a 22.81% increase, driven by renewed investor confidence in its clinical-stage pipeline and strategic advancements. The rally followed a critical milestone in the development of its lead drug candidate, hCDR1, a humanized monoclonal antibody targeting systemic lupus erythematosus and Sjögren’s syndrome. The asset, now in Phase II trials, has attracted attention due to its potential to address high-unmet medical needs in autoimmune diseases, a sector with growing therapeutic demand.

XTLB’s progress with hCDR1 is underpinned by a licensing agreement with Yeda Research and Development Company Ltd., a subsidiary of the Weizmann Institute of Science. This partnership provides

with exclusive rights to develop and commercialize the drug, reducing R&D risks and validating its scientific foundation. Success in Phase II trials could pave the way for partnerships with larger pharmaceutical firms, unlocking value through licensing deals or co-development agreements. Conversely, delays or adverse trial outcomes could dampen momentum, highlighting the stock’s sensitivity to clinical data.

The company’s recent acquisition of The Social Proxy, a web data AI firm, further diversified its intellectual property portfolio. While the immediate financial impact remains limited, the integration of AI tools into drug development processes—such as patient recruitment and trial design—signals a strategic pivot toward data-driven innovation. However, the long-term relevance of this acquisition to XTLB’s core biopharma operations remains to be proven, as the market evaluates whether the technology will enhance therapeutic outcomes or remain a peripheral asset.

Leadership changes also played a role in shaping investor sentiment. In April 2025, Noam Band was appointed as CEO, bringing experience from Teva Pharmaceutical Industries and Galmed Biopharma. His track record in scaling biotech firms has been interpreted as a stabilizing factor, particularly during the critical Phase II development phase of hCDR1. Yet, transitions in executive leadership carry inherent risks, including potential disruptions to R&D timelines or strategic realignments that could affect operational efficiency.

XTLB’s financial landscape remains challenging, with past Nasdaq notifications over minimum bid price requirements underscoring liquidity concerns. The company’s reliance on private placements, such as a $1.5 million raise in 2024, highlights its need for continuous capital infusions. While its operations in Israel offer access to skilled talent and government incentives, geopolitical tensions in the region could introduce operational and reputational risks for foreign investors.

Overall, XTLB’s stock performance reflects a delicate balance between clinical progress and financial realities. The biotech sector’s inherent volatility, coupled with macroeconomic uncertainties, means the stock’s trajectory will depend on near-term trial updates, capital-raising success, and Band’s ability to execute a coherent growth strategy. Investors are likely to remain closely attuned to these dynamics as the company navigates the high-stakes path from clinical development to commercialization.

https://www.ainvest.com/news/xtlb-stock-surges-22-81-phase-ii-hcdr1-milestone-yeda-licensing-deal-2510/

AlphaTON, Cyncado Unit in Digital Assets-Mesothelia Oncology Scheme

 Landmark Initiative Positions AlphaTON at Forefront of Decentralized Science (DeSci) Movement, Leveraging TON Infrastructure to Accelerate Life-Saving Cancer Research

AlphaTON Capital Corp (Nasdaq: ATON) ("AlphaTON" or the "Company"), alongside its wholly owned oncology subsidiary Tarus Therapeutics, LLC (dba Cyncado Therapeutics) ("Cyncado"), today announced a groundbreaking non-binding letter of intent (LOI) to evaluate tokenization of single-indication economics for TT-4 in mesothelioma, representing a transformative step in merging institutional-grade digital asset infrastructure with breakthrough cancer therapeutics.

This pioneering initiative exemplifies AlphaTON's unique position as the only Nasdaq-listed company simultaneously operating a strategic TON token treasury and advancing potentially first-in-class immunotherapy assets. The Company is leveraging decentralized science (DeSci) principles and web3 infrastructure to reimagine how life-saving medical research is funded, accelerated, and brought to patients globally. 

Bridging Two Frontiers: Digital Assets Meet Life-Saving Science

AlphaTON's strategic vision unites two high-impact domains previously operating in parallel: the Company's comprehensive TON ecosystem operations - including validator services, network staking, and Telegram-based application development serving over one billion users - with Cyncado's clinical-stage pipeline targeting immune checkpoint resistance in deadly cancers.

"We are witnessing the birth of a new paradigm in biomedical innovation," said Brittany Kaiser, Chief Executive Officer of AlphaTON Capital. "By thoughtfully integrating our digital asset capabilities with Cyncado's compelling oncology programs, we're not just exploring novel financing mechanisms, we're pioneering the future of decentralized science. This approach has the potential to democratize access to groundbreaking cancer research, accelerate development timelines, and create unprecedented alignment between global stakeholders and patient outcomes."

The mesothelioma tokenization initiative represents the first step in what could become a transformative model for funding and advancing therapeutic development through decentralized infrastructure, while preserving all traditional partnership, licensing, and exit pathways. Coupled with TON’s infinite sharding paradigm (ISP) data architecture, this new advancement not only has the opportunity to safeguard quality of life for patients, but also HIPAA-compliant data ownership and security for sensitive clinical on-chain data applications.

Clinical Momentum: TT-4 Advancing Toward Patients in Q1 2026

Cyncado has confirmed it is in final clinical start-up preparations for TT-4, an oral, ultra-selective A2B receptor antagonist, with first-patient dosing targeted for Q1 2026. The drug will initially enter a safety dose-escalation cohort enrolling solid tumor patients under Cyncado's existing FDA-cleared TT-10-101 (ADPORT-601) protocol, with a larger mesothelioma-focused study planned immediately thereafter at major U.S. cancer centers.

Mesothelioma, an aggressive cancer primarily caused by asbestos exposure, represents a significant unmet medical need with limited treatment options and poor prognosis. TT-4's preclinical data demonstrate compelling potential:

  • >90% tumor growth inhibition in murine mesothelioma models when combined with anti-PD1 antibody
  • 60% complete responses when combined with anti-PD-1 therapy
  • >90-day survival in combination treatment groups
  • Mechanistic validation supports TT-4’s potential to fully neutralize adenosine-mediated immune suppression, enhance anti-tumor responses, and broaden the impact of immunotherapy in mesothelioma
  • Superior single-agent activity compared to anti-PD-1 checkpoint inhibitors in head-to-head model comparisons

"The scientific and clinical community's response to our mesothelioma program has been extraordinarily positive," said Peter Molloy, Chief Executive Officer of Cyncado Therapeutics. "Key opinion leaders in the U.S. and internationally recognize the urgent need for new approaches in this devastating disease. We are in active discussions with leading non-U.S. investigators regarding additional mesothelioma studies that would complement our planned U.S. clinical program, potentially accelerating global development and patient access."

Decentralized Science: A New Model for Medical Innovation

The DeSci movement represents a fundamental reimagining of how scientific research is funded, conducted, and shared. By leveraging blockchain technology and tokenization, DeSci aims to:

  • Democratize research funding by enabling global participation in supporting promising therapeutic programs
  • Accelerate development timelines through efficient capital deployment and stakeholder alignment
  • Enhance transparency in clinical development and data sharing
  • Create direct value alignment between research supporters and therapeutic success
  • Reduce traditional barriers to advancing innovative medicines to patients in need

AlphaTON's exploration of tokenizing mesothelioma program economics positions the Company at the vanguard of this movement, combining proven Nasdaq governance standards with cutting-edge decentralized infrastructure.

"This is about more than innovation in capital formation," Kaiser continued. "We're building bridges between Telegram's billion-user platform, the TON ecosystem's powerful infrastructure, and breakthrough cancer research that could save lives. Every element of AlphaTON's business model is designed to create synergies - our validator operations strengthen network security, our ecosystem investments drive utility and adoption, and now our therapeutic programs demonstrate how DeSci can accelerate the path from laboratory to patient."

Preserving Optionality, Maximizing Impact

The LOI is exploratory and non-binding, with no commercial terms or structures finalized. Critically, any potential tokenization framework is being designed to preserve, not replace, all traditional pathways for therapeutic development, including conventional partnerships, strategic licensing, acquisition opportunities, and institutional financing.

Any future transaction would require board approval, regulatory clearance, and full compliance with applicable securities laws and regulations. This communication shall not constitute an offer to sell or the solicitation of an offer to sell or the solicitation of an offer to buy any securities, nor shall there be any sale of securities in any jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such jurisdiction. 

About AlphaTON Capital Corp

AlphaTON Capital is a specialized digital asset treasury company focused on building and managing a strategic reserve of TON tokens and developing the Telegram ecosystem. The Company implements a comprehensive treasury strategy that combines direct token acquisition, validator operations, and strategic ecosystem investments to generate sustainable returns for shareholders. Through its operations, AlphaTON Capital provides public market investors with institutional-grade exposure to the TON ecosystem and Telegram's billion user platform while maintaining the governance standards and reporting transparency of a Nasdaq listed company.

https://finviz.com/news/186697/alphaton-capital-and-subsidiary-cyncado-therapeutics-pioneer-convergence-of-digital-assets-and-oncology-innovation-exploring-tokenization-framework-for-mesothelioma-program-as-it-advances-toward-q1-2026-first-patient-dosing

'Von der Leyen calls for urgent response to Russia'

 European Commission President Ursula von der Leyen said on Wednesday that the recent Russian actions against European Union nations, including drone and jet incursions, cyberattacks and election meddling, are part of a "coherent and escalating campaign to unsettle our citizens, test our resolve, divide our union and weaken our support for Ukraine." She said they amount to a "gray zone" of hybrid warfare, which requires a "completely new mindset."

Von der Leyen said the Commission will present a readiness roadmap in two weeks, which will "not only set common objectives but also very concrete milestones and timelines on the way to 2030." The roadmap will include the development of airspace defenses, such as the drone wall, boosting the EU's critical capabilities, and strengthening defense manufacturing. "Europe must urgently equip itself with the strategic capacity to respond, one that is ready to address the changing nature of warfare," she told the European Parliament.

https://breakingthenews.net/Article/Von-der-Leyen-calls-for-urgent-response-to-Russia/64943520

Fed: Most participants think it's appropriate to ease further

 The Federal Open Market Committee (FOMC) released its minutes from the September meeting on Wednesday, detailing that most participants thought that it would likely be appropriate to "ease policy further over the remainder of this year."

Meanwhile, some participants were of the opinion that "financial conditions suggested that monetary policy may not be particularly restrictive, which they judged as warranting a cautious approach in the consideration of future policy changes."

https://breakingthenews.net/Article/Fed:-Most-participants-think-it's-appropriate-to-ease-further/64948179

France’s defense industry faces $17B funding gap to meet NATO goals

 France's defense sector will need an additional €15 billion ($17.4 billion) over the next several years if the country is to meet NATO targets.

https://seekingalpha.com/news/4502661-france-s-defense-industry-faces-17b-funding-gap-to-meet-nato-goals

Quantum BioPharma Cash Reward up to USD $7M for Proof of Market Manipulation

 Quantum BioPharma Ltd. (NASDAQ: QNTM) (CSE: QNTM) (FRA: 0K91) (Upstream: QNTM) (“Quantum BioPharma” or the “Company”), a biopharmaceutical company dedicated to building a portfolio of innovative assets and biotech solutions for the treatment of challenging neurodegenerative and metabolic disorders and alcohol misuse disorders with drug candidates in different stages of development, is pleased to announce a public whistleblower policy with a potential cash reward of up to USD $7 million to any individual or entity who can provide definitive and verifiable proof that they were asked, instructed, hired, or otherwise induced to manipulate the Company’s stock. The following individuals or entities are not eligible to receive rewards: 1) current directors, officers, or employees of the Company; 2) members of law enforcement, regulatory agencies, or government officials acting in an official capacity; 3) individuals who obtained information unlawfully or in violation of legal or professional duties; and 4) individuals who knowingly submit false, misleading, or fabricated information. The Company will not use the information until the information provider gives consent to the Company to use the information. Those with information can submit directly to reward@quantumbiopharma.com or call 1-833-571-1811.

When formulating this whistleblower reward and policy, Quantum BioPharma received legal opinions and comprehensive advice from multiple law firms/legal counsel, as well as the approval of its audit committee and its board of directors.

The cash reward of up to USD $7 million will be paid if that information tangibly and significantly contributes evidence which leads to a final, non‑appealable judgment in favour of the Company, or a binding settlement. This information includes, but is not limited to, evidence of tactics used such as: 1) illegal “spoofing” trades or, at another’s behest; 2) the deliberate spreading of false or misleading information about the Company across the internet; 3) selling shares that are not timely delivered; and 4) lending shares you do not have.

The whistleblower reward will only be paid out from the net proceeds of the Company’s ongoing lawsuit, once resolved. This reward can be shared between multiple parties providing different information.

The determination of any reward amount is at the Company’s discretion and based on the significance and impact of the information. Any information provided will be kept confidential, unless required by law. Information will only be used once written consent has been obtained.

The lawsuit, and this whistleblower reward, underscore the Company’s commitment to holding alleged perpetrators accountable, and helping restore market integrity.

https://www.globenewswire.com/news-release/2025/10/08/3163260/0/en/Quantum-BioPharma-Announces-Cash-Reward-of-up-to-USD-7Million-for-Proof-of-Market-Manipulation-in-its-Stock.html

Edwards Lifesciences slips as Oppenheimer downgrades

 Shares of Edwards Lifesciences (NYSE:EW) fell on Wednesday after Oppenheimer downgraded the cardiac device maker to Perform from Outperform, citing concerns over two upcoming trial readouts for the company’s Sapien line of heart valves.

The rating change comes as the Irvine, California-based MedTech is set to take part in the annual Transcatheter Cardiovascular Therapeutics (TCT) conference later this month to present data from its PARTNER-3 and ENCIRCLE trials.

Analyst Suraj Kalia argued that data from the trials, designed to evaluate Edwards’ (NYSE:EW) SAPIEN 3 and SAPIEN M3 heart valve systems, respectively, are unlikely to be “straightforward, and ensuing post-hoc debate could paint a confusing picture.”

“Our caution stems from our fundamental analysis on key product designs, statistical analysis of trial outcomes, and proprietary survey,” the analyst wrote, removing his price target on the stock.

Oppenheimer’s downgrade on Edwards (NYSE:EW) comes a day after Evercore ISI upgraded the company to outperform from equal weight, citing a near-term turnaround in its topline performance.  

https://www.msn.com/en-us/money/markets/edwards-lifesciences-slips-as-oppenheimer-downgrades-on-upcoming-data/ar-AA1O5oCa