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BioWorld - Tuesday, December 23, 2025
Breaking News: BioWorld 2025 Year in ReviewBreaking News: Trump administration impacts continue to roil the life sciences sectorBreaking News: Trump administration impacts continue to roil the life sciences sector
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Abbvie adds to in vivo CAR T efforts via $2.1B Capstan buy

June 30, 2025
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Abbvie Inc. is shelling out up to $2.1 billion to acquire CAR T player Capstan Therapeutics Inc., gaining rights to a phase I-stage program targeting CD19 as well as an in vivo cell engineering platform. The announcement comes on the heels of recently published data detailing Capstan’s delivery approach using targeted lipid nanoparticles (tLNPs) and marks Abbvie’s latest foray into the CAR T space.
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Elderly hands holding broken brain structure

Xpro phase II miss as Inmune’s Mindful tunes in to AD subgroup

June 30, 2025
By Randy Osborne
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Inmune Bio Inc. claimed a phase II win with TNF inhibitor Xpro (pegipanermin) in early Alzheimer’s disease (AD), though the study missed its primary and secondary endpoints, leading shares of the firm (NASDAQ:INMB) to close at $2.16, down $3.18, or almost 60%.
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Biopharma money raised: Jan. 1-June 26, 2025

June 27, 2025
Year-to-date money raised in public, private and other financings of biopharma companies.
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Money raised by biopharma

June 27, 2025
Total raised in public, private and other financings of biopharma companies, comparing 2019-2024.
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U.S. Supreme Court

Supreme Court upholds ACA’s preventive care coverage

June 27, 2025
By Annette Boyle
The U.S. Supreme Court preserved the U.S. Preventative Services Task Force coverage mandate that requires payers to cover certain preventive services at no cost to patients in a 6-3 ruling. That’s very good news for many diagnostics companies including Exact Sciences Corp. and Guardant Health Inc. as well as companies that manufacture HIV pre-exposure prophylaxis (PReP) medications such as Gilead Sciences Inc.
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Laptop displaying FDA logo

FDA waffles on post-assessment reports in final guidance for RRAs

June 27, 2025
By Mark McCarty
Industry’s reaction to the U.S. FDA’s draft guidance for remote regulatory assessments included a request for more clarity on when the agency would issue a post-assessment report, but the final guidance makes clear the FDA sees no compelling reason to issue such a report in every instance.
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China’s NMPA accepts Carsgen’s NDA for Claudin18.2-targeted CAR T​

June 27, 2025
A preview of the next edition of BioWorld, June 27, 2025
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Regulatory actions for June 27, 2025

June 27, 2025
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Aldeyra, Biocity, Carsgen, Emmaus, Pint, Theravance, Viatris.
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Other news to note for June 27, 2025

June 27, 2025
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: CDR-Life, CSL, Hummingbird, Kalvista, Northern Antibiotics, Novartis, Pendopharm, Percheron, Profound, Prokaryotics, Valneva.
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In the clinic for June 27, 2025

June 27, 2025
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Alebund, Altimmune, Alto, Crispr, Edgewise, Gri, I-Mab, Invivyd, Lisata, Metabolics, Opus, Pfizer, Viatris.
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