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BioWorld - Wednesday, May 14, 2025
Breaking News: US FDA clears Abbvie’s c-Met lung cancer ADC Breaking News: 100 days of uncertaintyBreaking News: 100 days of uncertainty
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Make-or-break adcom next step for Stealth’s Barth syndrome drug

Oct. 8, 2024
By Mari Serebrov
Stealth Biotherapeutics Inc. had hoped the U.S. FDA would have approved its lead candidate, elamipretide, as the first treatment for Barth syndrome by now. Instead, it’s headed to a meet-up with the agency’s Cardiovascular and Renal Drugs Advisory Committee (CRDAC) Oct. 10. The discussion and vote at that meeting could be make-or-break for patients with the ultra-rare debilitating mitochondrial disease that has no approved therapies. “Barring support from CRDAC, the future of elamipretide for Barth syndrome in the U.S. is tenuous," Stealth CEO Reenie McCarthy told BioWorld.
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Seniors with wooden puzzle

Sage stumbles in Alzheimer’s while awaiting Huntington’s data

Oct. 8, 2024
By Lee Landenberger
Bad news has buffeted Sage Therapeutics Inc. twice in the past few months. Now its placebo-controlled phase II Lightwave study of dalzanemdor in Alzheimer's disease has missed the primary outcome measure, prompting the company to stop development of the NMDA receptor positive allosteric modulator in the indication.
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Brain and DNA

Aviadobio, Astellas ink $2B+ frontotemporal dementia gene therapy deal

Oct. 8, 2024
By Nuala Moran
Aviadobio Ltd. has entered a potential $2.18 billion license and commercialization agreement for its frontotemporal dementia gene therapy, AVB-101, with Astellas Pharma Inc. Astellas is making a $20 million equity investment in London-based Aviadobio and will pay up to $30 million up front in advance of deciding whether or not to exercise the exclusive option to worldwide rights.
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Mestag’s activated fibroblast approach draws Merck in $1.9B deal

Oct. 8, 2024
By Nuala Moran
Mestag Therapeutics Ltd. has sealed a potential $1.9 billion agreement with Merck & Co. Inc., in which it will apply its expertise in activated fibroblasts to identify novel targets for inflammatory diseases. The pharma company has the option to license one or more targets, up to a prespecified number, and will take on all subsequent discovery, development and commercialization work.
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Wuhan YZY, CTTQ ink $143M China bispecific antibody deal

Oct. 8, 2024
By Tamra Sami
Wuhan YZY Biopharma Co. Ltd. is out-licensing lead candidate M-701, a CD3/EpCAM bispecific antibody, to Chia Tai Tianqing Pharmaceutical Group Co. Ltd. (CTTQ) for China rights in a deal worth up to $143 million. Under the deal, Sino Biopharmaceutical Ltd. subsidiary CTTQ is granted an exclusive license to develop, register, manufacture and commercialize M-701 within mainland China.
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Other news to note for Oct. 8, 2024

Oct. 8, 2024
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Galecto, Kronos, Onkure, Reneo.
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In the clinic for Oct. 8, 2024

Oct. 8, 2024
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Astrazeneca, Avillion, Bergenbio, GE Healthcare, Hansa, Insignis, Johnson & Johnson, Kalvista, Scholar Rock.
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Financings for Oct. 8, 2024

Oct. 8, 2024
Biopharmas raising money in public or private financings, including: Biovaxys, CK Life Sciences, Camp4, IMV, Rege Nephro, Upstream, Virios, Wex.
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Appointments and advancements for Oct. 8, 2024

Oct. 8, 2024
New hires and promotions in the biopharma industry, including: Cytodyn, KSQ, Opthea, Optinose, Tourmaline.
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Regulatory actions for Oct. 8, 2024

Oct. 8, 2024
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: .
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