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OS Therapies Applauds Reauthorization of Pediatric Priority Review Voucher Program to Advance Breakthrough Osteosarcoma Immunotherapies
New York, New York--(Newsfile Corp. - February 4, 2026) - OS Therapies Inc. (NYSE American: OSTX) ("OS Therapies" or "the Company"), the world leader in listeria-based cancer immunotherapies, is honored to celebrate the passage of the Mikaela Naylon Give Kids A Chance Act. Mikaela, like so many other children, courageously battled pediatric cancer - specifically Osteosarcoma. Her legacy through this legislation will accelerate critical opportunities for research and therapeutic access for other.
About this update from Os Therapies Incorporated
[{"type":"text","content":"New York, New York--(Newsfile Corp. - February 4, 2026) - OS Therapies Inc. (NYSE American: OSTX) ("OS Therapies" or "the Company"), the world leader in listeria-based cancer immunotherapies, is honored to celebrate the passage of the Mikaela Naylon Give Kids A Chance Act. Mikaela, like so many other children, courageously battled pediatric cancer - specifically Osteosarcoma. Her legacy through this legislation will accelerate critical opportunities for research and therapeutic access for other children and teens currently living with pediatric cancers.","length":579,"tagName":"p"},{"type":"text","content":"Innovation is urgent and direly needed as pediatric cancers remain the leading disease-based cause of pediatric death in the United States. OS Therapies is empowered to continue its groundbreaking work combating osteosarcoma, where there is still significant unmet need for patients - primarily children and teens.","length":314,"tagName":"p"},{"type":"text","content":"Through the reauthorization of the Rare Pediatric Disease Designation (RPDD) Priority Review Voucher (PRV) program, OS Therapies can continue their dedicated efforts with an extended deadline for the Company to receive a Biologics License Application (BLA) for OST-HER2 in the prevention or delay of recurrent, fully resected, pulmonary metastatic osteosarcoma. The Company will now remain eligible to receive a PRV from September 30, 2026, to September 30, 2029.","length":463,"tagName":"p"},{"type":"text","content":"The reauthorization of the program also incentivizes OS Therapies to re-evaluate the development of other pipeline products across its listeria-based cancer immunotherapy platform in the context of potential additional PRV opportunities, and benefits afforded by the FDA Platform Technology Designation Program for Drug Development. The Company will provide further details regarding the outcome of this evaluation process after the current sequence of marketing authorization submissions for its lead osteosarcoma candidate is completed.","length":538,"tagName":"p"},{"type":"text","content":"OS Therapies is grateful for the positive impact of Mikaela's and some many other patients' legacy, and the Company is committed to building upon it to transform the lives of children and teens living with osteosarcoma and other rare cancers.",...