Bridgebio Pharma Announced It Has Surpassed Its Interim Analysis Enrollment Target For BBP-418 And Expects Topline Interim Data From Its Phase 3 FORTIFY Study For Limb-girdle Muscular Dystrophy Type 2I/R9 In 2025
Portfolio Pulse from Benzinga Newsdesk
BridgeBio Pharma has surpassed its interim analysis enrollment target for its Phase 3 FORTIFY study of BBP-418 for Limb-girdle Muscular Dystrophy Type 2I/R9, with top-line results expected in 2025. The company is considering pursuing Accelerated Approval for BBP-418 following recent interactions with the FDA.
June 18, 2024 | 11:36 am
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BridgeBio Pharma has surpassed its enrollment target for the Phase 3 FORTIFY study of BBP-418, with top-line results expected in 2025. The company is considering pursuing Accelerated Approval for BBP-418 following recent FDA interactions.
Surpassing the enrollment target for a Phase 3 study is a significant milestone, indicating progress in the clinical trial. The potential for Accelerated Approval and the Rare Pediatric Disease Designation add further positive sentiment, likely boosting investor confidence.
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