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BioWorld - Saturday, February 14, 2026
Breaking News: BioWorld 2025 Year in ReviewBreaking News: Trump administration impacts continue to roil the life sciences sector
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Holiday notice

Jan. 21, 2025
BioWorld's offices were closed in observance of Martin Luther King Jr. Day in the U.S. No issue was published Monday, Jan. 20.
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Hope in OTC as Iecure’s in vivo gene editing trial shows first response

Jan. 21, 2025
By Nuala Moran
A 6.5-month-old boy with the rare inherited urea cycle disorder ornithine transcarbamylase (OTC) deficiency has responded positively in a targeted in vivo gene editing trial, in which a correct copy of a defective gene was inserted at a precise locus in the genome.
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FDA approves Daiichi Sankyo’s Trop-2 ADC for breast cancer

Jan. 21, 2025
By Tamra Sami
Marking the second global approval after Japan, the U.S. FDA has approved Datroway (datopotamab deruxtecan), a trophoblast cell surface antigen 2-directed antibody-drug conjugate (ADC) from Daiichi Sankyo Co. Ltd. and Astrazeneca plc, for treating adults with hormone receptor-positive, HER2-negative unresectable or recurrent breast cancer after prior chemotherapy.
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3d rendering of bispecific antibodies

Newco Prolium licenses antibody from Innocare, Keymed for $520M

Jan. 21, 2025
By Tamra Sami
In another Chinese newco out-licensing deal, Innocare Pharma Ltd. and Keymed Biosciences Co. Ltd. out-licensed their co-developed CD20×CD3 bispecific antibody (ICP-B02/CM355) to startup Prolium Bioscience Inc. in a deal worth up to $520 million.
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Prepping for $1B in cuts, Moderna gets a $590M BARDA boost

Jan. 21, 2025
By Lee Landenberger
While Moderna Inc. plans to cut its expenses by $1 billion in 2025, the company has received a little breathing room by a hefty U.S. Department of Health and Human Services (HHS) grant. The Biomedical Advanced Research and Development Authority awarded Moderna roughly $590 million to support late-stage development of its mRNA-based avian-variant vaccines and to increase the number of clinical trials for another five additional subtypes of pre-pandemic influenza.
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One dice with a green checkmark, red X and gray question mark.

Sage lawsuit enforces standstill as board evaluates Biogen offer

Jan. 21, 2025
By Karen Carey
A series of disappointments that drove Sage Therapeutics Inc.’s stock down by 85% since August of 2023 has evolved into an unsolicited takeout offer by partner Biogen Inc., followed by a lawsuit filed by Sage a week later. The two parties, both of Cambridge, Mass., first partnered in a $1.52 billion deal in 2020, primarily to develop Zurzuvae (zuranolone) for depression. The deal included Biogen taking a 10.2% equity stake in Sage, paying $104.14 per share, or $650 million total.
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Regulatory actions for Jan. 21, 2025

Jan. 21, 2025
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Aosaikang, Amgen, Astrazeneca, Foundation Medicine, Impact, Innovent, Junshi, Telix, Topalliance, Zai Lab.
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Other news to note for Jan. 21, 2025

Jan. 21, 2025
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Scilex, Romeg.
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In the clinic for Jan. 21, 2025

Jan. 21, 2025
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Boehringer Ingelheim, Novo Nordisk.
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Financings for Jan. 21, 2025

Jan. 21, 2025
Biopharmas raising money in public or private financings, including: Phio.
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