BridgeBio’s infigratinib shows improved apnea and ear-infection trends in PROPEL 3

Verifying
  • BridgeBio Pharma shared 52-week PROPEL 3 data for oral infigratinib in children with achondroplasia.
  • AHI increased 10.4% with infigratinib versus 49.2% with placebo.
  • BridgeBio submitted an FDA application and expects a U.S. launch in mid-2027.
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