Anavex Life Sciences to Present at the 25th Annual Needham Virtual Healthcare Conference

On April 7, 2026 Anavex Life Sciences Corp. ("Anavex" or the "Company") (Nasdaq: AVXL), a clinical-stage biopharmaceutical company focused on developing innovative treatments for Alzheimer’s disease, Parkinson’s disease, schizophrenia, neurodevelopmental, neurodegenerative, and rare diseases, including Rett syndrome, and other central nervous system (CNS) disorders, reported that it will present at the 25th Annual Needham Virtual Healthcare Conference, April 13 – 16, 2026. President and Chief Executive Officer Christopher U. Missling, PhD and his management team will present the Company scheduled at 1:30 PM (ET) on Tuesday, April 14th, 2026.

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A live audio webcast will be accessible through the Investors section of the Company’s website at www.anavex.com. An archived edition of the session will be available later that day.

(Press release, Anavex Life Sciences, APR 7, 2026, View Source [SID1234664199])

Alloy Therapeutics Enters into Multi-Target Collaboration and License Agreement with Biogen for Use of Alloy’s AntiClastic™ ASO Platform

On April 7, 2026 Alloy Therapeutics Inc. ("Alloy"), a biotechnology ecosystem company dedicated to democratizing access to cutting-edge drug discovery technologies, reported a collaboration and license agreement with Biogen Inc. for the use of Alloy’s novel and proprietary AntiClastic ASO Platform. Through this collaboration, Biogen will apply the platform to advance antisense therapeutics against multiple undisclosed targets. Alloy will receive an upfront payment and is eligible for additional milestone payments and tiered royalties on any products resulting from the collaboration.

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The collaboration and license agreement brings together Biogen’s scientific leadership and experience in advancing innovative medicines with Alloy’s proprietary antisense discovery capabilities. Alloy’s AntiClastic ASO platform enables drug developers to realize the full potential of antisense therapeutics by reaching intracellular disease targets at the RNA level. The platform is specifically designed to address potency and therapeutic index challenges that have historically held back the promise of antisense drugs due to limited biodistribution and, therefore, efficacy.

"Biogen has built an extraordinary reputation for scientific leadership and for translating breakthrough research into impactful therapies," said Errik Anderson, CEO and Founder of Alloy Therapeutics. "We value our long-standing relationship and are honored to support their world-class teams with access to our AntiClastic ASO Platform and broader technology ecosystem, helping enable the continued pursuit of innovative treatments that have the potential to change patients’ lives."

"This collaboration reflects Biogen’s commitment to pushing the boundaries of scientific innovation and exploring novel approaches to address complex diseases," said Jane Grogan, Ph.D., Executive Vice President and Head of Research at Biogen. "Partnering with Alloy allows us to expand our research strategies and continue advancing programs with the potential to benefit patients worldwide."

Alloy’s capabilities span an integrated ecosystem of drug discovery platforms designed to accelerate the development of innovative therapeutics. The company continues to integrate advanced technologies, including computational and AI-enabled approaches, to enhance discovery and optimization across its programs.

About the Alloy Therapeutics Genetic Medicines AntiClastic ASO Platform

The AntiClastic ASO platform designs novel oligonucleotide formats, exclusively available through partnerships with Alloy’s Genetic Medicines division, to overcome potency and therapeutic index challenges that have historically limited the promise of antisense drugs. Dr. Sudhir Agrawal invented the core technology, which combines improvements in the primary sequence with a proprietary spatial conformation of nucleic acid drugs to promote the delivery of antisense to target RNA, mitigate the inflammatory response, and improve a drug’s therapeutic index. The resulting drug candidates have shown a significant increase in potency compared to gapmer antisense formats. Partners can apply this format to existing antisense sequences or partner to discover new AntiClastic oligonucleotide molecules to precisely deliver therapeutic payloads to their intended target.

(Press release, Alloy Therapeutics, APR 7, 2026, View Source [SID1234664198])

RS Research Announces Successful Completion of Phase 1 Clinical Trial of RS-0139 in Solid Tumors

On April 6, 2026 RS Research, a biotechnology company developing smart nanomedicines for oncology, reported the successful completion of the Phase 1 clinical trial of its lead investigational candidate RS-0139 in patients with solid tumors. Designed on the company’s proprietary Sagitta platform to selectively deliver docetaxel to tumor tissue and improve therapeutic index, RS-0139 has now generated early clinical evidence supporting not only its own continued advancement, but also the broader translational potential of the Sagitta platform. This milestone marks an important inflection point for RS Research as it prepares for the next stage of development, including international clinical expansion, strategic partnering and future financing discussions.

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The completed Phase 1 clinical study was a multicenter, open-label, two-step Phase 1a/1b trial conducted to determine the optimum dose and characterize pharmacokinetic, safety and tolerability profile of RS-0139 in patients with recurrent, locally advanced or metastatic solid tumors. The study generated the initial clinical dataset needed to assess how Sagitta-enabled targeted delivery may translate into an improved therapeutic index in a real-world oncology setting.
Key findings from the Phase 1 trial include:

• markedly improved hematologic safety compared with conventional chemotherapy,
• an encouraging overall safety and tolerability profile,
• promising early signals of antitumor activity.

RS Research is currently consolidating the full clinical dataset and completing the relevant procedural steps in preparation for future scientific and corporate disclosure of additional details.

Prof. Rana Sanyal, Co-Founder and CSO of RS Research, and Grand Prize Laureate of the EIC European Prize for Women Innovators, said: "These results are the product of years of rigorous science, persistence and translational focus. More importantly, they provide early clinical validation of our Sagitta platform, supporting our confidence that targeted delivery can meaningfully improve the therapeutic index of oncology treatments. This milestone strengthens our conviction in advancing additional candidates built on the same platform."

Sagitta is RS Research’s proprietary drug delivery platform, designed to improve therapeutic index by selectively directing cytotoxic payloads to tumor tissue and addressing the longstanding efficacy-toxicity trade-off in solid tumors.

Gülsah Nomak, MD, Medical Director of RS Research, stated: "The successful completion of the Phase 1 program provides the clinical foundation for our next stage of development. It supports our plans to advance RS-0139 into an international Phase 2 program designed to further define its therapeutic potential in solid tumors."

Dr. Sena Nomak, Co-Founder and COO of RS Research, added: "This milestone marks an important point of transition for RS Research as we move from early clinical validation toward broader international development. We have secured over 20 million USD backing so far from pharma, VC and non-dilutive funding sources. It strengthens our position in ongoing strategic discussions around the company’s global growth trajectory and comes at a meaningful time as we prepare for our upcoming Series B financing round."

(Press release, RS Research, APR 6, 2026, View Source [SID1234664623])

Stipple Bio Emerges From Stealth with Oversubscribed $100 Million Series A Financing to Advance STP-100 into Early Clinical Studies and Advance a Precision Oncology Pipeline that Leverages its Pointillist Platform

On April 6, 2026 Stipple Bio, Inc., a private biotechnology company harnessing epitope-level precision to create targeted cancer therapies, reported the close of a $100 million heavily oversubscribed Series A financing. The financing was co-led by RA Capital, a16z Bio+Health and Nextech Invest, and includes participation from existing investors Emerson Collective Investments (managed by Yosemite), GV (Google Ventures), LoLa Capital Partners and GordonMD Global Investments, among others. In conjunction with the financing, Derek DiRocco, PhD and Thilo Schroeder, PhD will join the Stipple Bio Board of Directors which already includes Vineeta Agarwala MD, PhD, Owen Hughes, Jeff Landau and Aaron Ring MD, PhD and Greg Verdine, PhD.

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The proceeds from the financing, which should fund the company into 2029, will be used to advance its lead candidate, STP-100, into multiple early-stage clinical studies, and to leverage its Pointillist Platform to identify additional tumor-specific cell surface epitopes enabling the development of additional pipeline candidates with a high therapeutic index.

"We are building upon deep cancer biology expertise to map, target and unlock tumor-specific epitopes which enable us to develop a pipeline of next-generation precision oncology therapeutics," said Jeff Landau, Chief Executive Officer of Stipple Bio. "This funding positions us to progress STP-100 into the clinic and continue building a broad oncology pipeline. I am extremely pleased to have the support of industry-leading investors who share our enthusiasm towards developing precision and differentiated cancer therapies based on our modality-agnostic Pointillist Platform."

"Clinical experience with prior antibody drugs has taught us that epitope-level specificity matters. Since the earliest days of Stipple Bio, we’ve been impressed by the team’s vision to move beyond tumor-specific gene expression and to pioneer tumor-specific ‘epitomics’ in precision oncology. We are proud to have supported Stipple Bio since inception and to co-lead this financing as the company advances safer, more effective therapies for patients living with cancer," said Dr. Agarwala, General Partner at Andreessen Horowitz and lead investor for the a16z Bio+Health Fund.

"Stipple Bio’s Pointillist Platform introduces an epitope-level approach to targeting tumor biology that has the potential to meaningfully expand the set of druggable oncology targets. Lead candidate STP-100 illustrates how this strategy can drive precise tumor targeting while sparing normal tissues—a key step toward improving therapeutic index in ADCs. We are excited to partner with the team as they advance STP-100 into the clinic and build a broader pipeline from the platform," said Dr. DiRocco, Partner at RA Capital Management.

Stipple Bio was founded in 2022 by cancer biology pioneers Dr. Aaron Ring, Associate Professor, Translational Science and Therapeutics Division at Fred Hutch, and Dr. Aashish Manglik, Associate Professor, Pharmaceutical Chemistry at UCSF, both of whom believed that targeting tumor-specific cell surface epitopes could improve therapeutic index and unlock targets previously intractable with conventional oncology drug discovery methods. a16z Bio+Health, Emerson Collective Investments (managed by Yosemite) and OMX provided Stipple Bio’s initial Seed financing.

(Press release, Stipple Bio, APR 6, 2026, View Source [SID1234664197])

Geron to Participate in the 25th Annual Needham Virtual Healthcare Conference

On April 6, 2026 Geron Corporation (Nasdaq: GERN), a commercial-stage biopharmaceutical company aiming to change lives by changing the course of blood cancer, reported that members of the management team are scheduled to participate in a fireside chat at the 25th Annual Needham Virtual Healthcare Conference on Monday, April 13, 2026 at 11:00 a.m. ET.

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A live and archived audio webcast of the fireside chat will be available through the Investors & Media section of Geron’s website at www.geron.com.

(Press release, Geron, APR 6, 2026, View Source [SID1234664196])