BD completes enrollment in pivotal PREVENT trial for Phasix Mesh
Aug 12, 2026, 6:55 AM EDT1 sourcesAI-analyzed
Why it may matterVerify against the original reporting
Milestone completion reduces regulatory uncertainty and could unlock a path to FDA submission; successful data could broaden BD's TAM in surgical repair, supporting multiple-year growth catalysts, though near-term earnings impact remains uncertain.
AI summary
What happened, with direct paths to the underlying reporting
BD announced enrollment completion in PREVENT, the first large randomized trial of Phasix Mesh to prevent incisional hernias after open abdominal surgery. The study enrolled 477 patients across 32 sites in the US and Europe, with a 24-month primary endpoint and up to five years of follow-up, potentially supporting an FDA submission for this indication.
Enrollment completed in PREVENT trial evaluating Phasix Mesh for incisional hernia prevention. 477 patients across 32 sites in US/Europe.
Largest randomized prophylactic mesh trial; aims to support FDA submission. Primary endpoint at 24 months; long-term follow-up to five years.
Phasix Mesh is a resorbable mesh. BD aims to expand regenerative tech in surgery.
Primary endpoint readout planned at 24 months; data could support regulatory filing.
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