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BioWorld - Sunday, May 31, 2026
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Red and blue bispecific antibodies

Genmab adding late-stage bispecific in $8B Merus acquisition

Sep. 29, 2025
By Jennifer Boggs
No Comments
Genmab A/S is paying $8 billion to acquire Merus NV, gaining rights to the latter’s phase III-stage petosemtamab, a bispecific antibody initially in development for head and neck cancer, and continuing the firm’s strategy to transition from a royalty-based operation to a fully integrated biopharma.
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Money raised by biopharma

Sep. 26, 2025
Total raised in public, private and other financings of biopharma companies, comparing 2019-2025.
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Biopharma money raised: Jan. 1-Sept. 25, 2025

Sep. 26, 2025
Year-to-date money raised in public, private and other financings of biopharma companies.
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Trump hits drug imports with 100% tariffs, starting Oct. 1

Sep. 26, 2025
No Comments
A preview of the next edition of BioWorld, Sept. 26, 2025
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Regulatory actions for Sept. 26, 2025

Sep. 26, 2025
Regulatory snapshots, including global drug submissions and approvals, and other regulatory decisions and designations: Arialys, Biogen, Biostar, Eisai, Nrx, Vertex.
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Other news to note for Sept. 26, 2025

Sep. 26, 2025
Biopharma happenings, including deals and partnerships, and other news in brief: Cidara, Evaxion, Gossamer, Lunia Bioworks, Merck, Qurient, Respira, Synaffix, Tiziana, Verona.
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In the clinic for Sept. 26, 2025

Sep. 26, 2025
Clinical updates, including data readouts and publications: AC Immune, Clene, Hansa, Immuneering, Immunic, Intellia, Pepgen.
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Financings for Sept. 26, 2025

Sep. 26, 2025
Biopharmas raising money in public or private financings, including: Arecor, Drugs Made In America, Immuneering, Kalvista, Ligand, MBX, Pepgen, Sanofi.
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Appointments and advancements for Sept. 26, 2025

Sep. 26, 2025
New hires and promotions in the biopharma industry, including: 4M Therapeutics, AL-S Pharma, Annovis, Invivyd, LB Pharma, Nuvectis, Zealand.
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DNA in drug capsules

FDA continues to build regenerative medicine pathway

Sep. 26, 2025
By Mari Serebrov
No Comments
The U.S. FDA released a trio of draft guidances to help sponsors in developing and monitoring cell and gene therapies, as well as other regenerative medicine therapies.
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