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BioWorld - Saturday, May 2, 2026
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Hand holding FDA blocks

Uncertainty builds at US FDA with retirements, CR questions

Dec. 19, 2024
By Mari Serebrov
The end of the year will be the end of an era at the FDA, as Bob Temple shuts his door at CDER for the last time Dec. 31. After more than half a century at the FDA’s drug center, Temple has become the backbone of CDER’s new drug program, providing expertise and stability as other personnel have come and gone.
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Omeros, Prothena stocks climb on clinical data; Vertex slips

Dec. 19, 2024
By Karen Carey
Clinical data reported by a handful of biopharmas on Dec. 19 sent stocks soaring or plunging, as company leaders laid out next-step plans. Investors showed enthusiasm for Omeros Corp.’s narsoplimab to treat hematopoietic stem cell-transplant-associated thrombotic microangiopathy (TA-TMA), and Roche AG’s Parkinson’s prospect prasinezumab, which is partnered with Prothena Corp. plc.
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Any Betta? FDA adds Ensacove to ALK lung cancer weaponry

Dec. 19, 2024
By Randy Osborne
A Chinese player entered the U.S. non-small-cell lung cancer (NSCLC) arena as the U.S. FDA cleared Xcovery Holdings Inc.’s Ensacove (ensartinib) as a first-line therapy for adults with anaplastic lymphoma kinase (ALK)-positive locally advanced or metastatic disease who have not previously received an ALK-inhibitor. Xcovery, of Palm Beach Gardens, Fla., is a subsidiary of Betta Pharmaceuticals Co. Ltd, of Hangzhou, China.
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Silhouette of head and brain with DNA double helixes

Sangamo and Astellas link up in a $1.32B AAV deal

Dec. 19, 2024
By Lee Landenberger
Sangamo Therapeutics Inc.’s second large, worldwide licensing deal for its capsid technology in the past five months is with Astellas Pharma Inc. The California-based company is getting $20 million up front and the chance to bring in up to $1.3 billion in fees and milestone payments in an agreement spanning five potential disease targets for gene therapies to treat neurological diseases.
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3D illustration of mesenchymal stem cells

Mesoblast scores first US nod for mesenchymal stromal cell therapy

Dec. 19, 2024
By Tamra Sami
Regenerative medicine company Mesoblast Ltd. received an early Christmas present from the FDA for approval of its allogeneic bone marrow-derived mesenchymal stromal cell (MSC) therapy, Ryoncil (remestemcel-L), for steroid-refractory acute graft-vs.-host disease (SR-aGvHD) in children 2 months and older, including adolescents.
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Regulatory actions for Dec. 19, 2024

Dec. 19, 2024
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Agios, Celltrion, Eli Lilly, Johnson, Praxis.
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Other news to note for Dec. 19, 2024

Dec. 19, 2024
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Cara, Clarity, Catalent, Eli Lilly, Grit, Holoclara, Inceptor, Novo Nordisk, Photys, Structure, Tvardi, Ultimovacs, Zelluna.
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In the clinic for Dec. 19, 2024

Dec. 19, 2024
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Alk-Abello, Aurion, Cognition, Corvus, Ena, Exegi, Hansa, Krystal, Metavia, Mendus, Quoin, Sensorion, Transcode, Viatris, Verastem.
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Financings for Dec. 19, 2024

Dec. 19, 2024
Biopharmas raising money in public or private financings, including: Awakn, Siteone, Soleno, Tessera, Xbrane.
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Appointments and advancements for Dec. 19, 2024

Dec. 19, 2024
New hires and promotions in the biopharma industry, including: Gelteq, Lexeo, March, Marea, Polyrizon, Sanofi.
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