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Press Releases
Contrario Medical Receives FDA 510(k) Clearance for Cyperus Sperm Separation Device
November 2, 2026
·
2 min read
Press Releases
Roche receives FDA 510(k) clearance for new cobas® eplex respiratory pathogen panel 3, enabling labs to customize respiratory testing for local patient needs
November 2, 2026
·
4 min read
Press Releases
Seaport Therapeutics Reports Third Quarter 2026 Financial Results and Highlights Recent Corporate and Clinical Progress
November 2, 2026
·
12 min read
Press Releases
AN2 Therapeutics Receives U.S. FDA IND Clearance to Proceed with Planned Phase 2 Global Study of Oral Epetraborole in Polycythemia Vera
November 2, 2026
·
5 min read
Press Releases
Yarrow Bioscience Announces Participation in November 2026 Investor Events
November 2, 2026
·
4 min read
Press Releases
Tempus Reports Third Quarter 2026 Results
November 2, 2026
·
19 min read
Press Releases
LIB Therapeutics Sets $300 Monthly List Price for the Autoinjector Form of LEROCHOL® (lerodalcibep-liga), Lowering Costs and Expanding Access for Adults Living With High Cholesterol
November 2, 2026
·
8 min read
Press Releases
InMed Announces Share Consolidation in Connection with Proposed Merger
November 2, 2026
·
8 min read
Business
Karyopharm files for bankruptcy, looks to merger with Ayrmid for life raft
Debtor-in-process financing up to $55 million could keep the lights on at Karyopharm Therapeutics for its multiple myeloma and myelofibrosis programs as the biotech waits to see if its union with Ayrmid will go through.
November 2, 2026
·
3 min read
·
Angela Gabriel
Opinion
FDA peptide policy risks undermining drug development and patient safety
By allowing compounding pharmacies to produce certain unapproved peptides, the Department of Health and Human Services could, in the short term, put patients in harm’s way. Longer term, the policy shift threatens the industry that brings new medicines to market.
November 2, 2026
·
6 min read
·
Robert Popovian
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