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BridgeBio aces phase 3 rare disease test, clearing path to FDA (fiercebiotech.com)
1 point by randycupertino 43 days ago | hide | past | favorite | 1 comment


Exciting results for this rare genetic muscle-wasting disorder Limb-Girdle Muscular Dystrophy (LGMD2I/R9) trial, and sounds like the FDA is on board with the surrogate endpoint. Could be big validation for BridgeBio’s rare disease strategy.




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