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November 28, 2023
The approval is the first for a systemic therapy to treat desmoid tumors, offering patients an alternative to surgery.
September 13, 2023
Pti: Consider these 8 Factors before Scheduling your First Therapy Session
March 22, 2023
Biologics License Application (BLA) Resubmission for Pediatric Acute Graft-Versus-Host Disease (SR-aGVHD) Currently Being Reviewed PDUFA Goal Date...
January 25, 2023
The first topical in vivo gene therapy to reach late-stage development heals dystrophic epidermolysis bullosa wounds, researchers report.
May 12, 2022
~ FDA Prescription Drug User Fee Act (PDUFA) Target Action Date Set for September 23, 2022 ~ ~ If Approved by the FDA, PEDMARKTM Stands to Be the First...
May 12, 2022
Press release content from Globe Newswire. The AP news staff was not involved in its creation.
May 28, 2021
~ If Approved by the FDA, PEDMARK Stands to Be the First Therapy for the Prevention of Cisplatin-Induced Hearing Loss in Children ~ Research Triangle Park, NC, May 28 , 2021 - Fennec Pharmaceuticals Inc. (NASDAQ: FENC; TSX: FRX), a specialty pharmaceutical company, today announced the resubmission of its New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for PEDMARK TM (a unique formulation of sodium thiosulfate) for the prevention of ototoxicity induced by cisplatin che...