Vertex On Track To Submit New Drug Applications To The FDA By Mid-2024 For Both VX-548 In Acute Pain And The Vanzacaftor Triple In CF
Portfolio Pulse from Benzinga Newsdesk
Vertex Pharmaceuticals is on schedule to submit New Drug Applications (NDAs) to the FDA by mid-2024 for VX-548, aimed at treating acute pain, and the Vanzacaftor triple combination for Cystic Fibrosis (CF).
February 05, 2024 | 9:09 pm
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Vertex Pharmaceuticals is preparing to submit NDAs for VX-548 for acute pain and the Vanzacaftor triple for CF by mid-2024.
The submission of NDAs for VX-548 and the Vanzacaftor triple indicates significant progress in Vertex's pipeline, potentially leading to new revenue streams upon approval. This development is likely to be viewed positively by investors, reflecting optimism about the company's future prospects and its ability to innovate in the treatment of acute pain and CF.
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