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Home » Newsletters » BioWorld

BioWorld

Jan. 21, 2025

View Archived Issues
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Sage lawsuit enforces standstill as board evaluates Biogen offer

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. Read More

Prepping for $1B in cuts, Moderna gets a $590M BARDA boost

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. Read More
3d rendering of bispecific antibodies

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

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. Read More

Hope in OTC as Iecure’s in vivo gene editing trial shows first response

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. Read More
Drug-development

Mapping GLP-1RA effects turns up benefits, risks, ‘master lessons in biology’

The largest analysis to date of patients taking GLP-1 receptor agonists (GLP-1RAs) has investigated their effects on nearly 175 diseases, and found that compared to three other classes of diabetes medications, individuals with a prescription for GLP-1RAs had a reduced risk of 42 diseases, and an increased risk of 19. Read More

FDA approves Daiichi Sankyo’s Trop-2 ADC for breast cancer

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. Read More

Holiday notice

BioWorld's offices were closed in observance of Martin Luther King Jr. Day in the U.S. No issue was published Monday, Jan. 20. Read More

ICYMI: Week in review, Jan. 13-17, 2025

A quick look back at top stories. Read More

Biggest gainers and losers for Jan. 13-17, 2025

The top 10 biopharma stock gainers and losers for the week. Read More

Appointments and advancements for Jan. 21, 2025

New hires and promotions in the biopharma industry, including: Applied, Aravax, Artbio Compass Pathways, Kincell, Marea, Oragenics, Oryzon, Pacira, Pharming, Sumitomo. Read More

Financings for Jan. 21, 2025

Biopharmas raising money in public or private financings, including: Phio. Read More

In the clinic for Jan. 21, 2025

Clinical updates, including trial initiations, enrollment status and data readouts and publications: Boehringer Ingelheim, Novo Nordisk. Read More

Other news to note for Jan. 21, 2025

Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Scilex, Romeg. Read More

Regulatory actions for 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. Read More

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