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BMY — Bristol-Myers Squibb News Story

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Brief: Bristol Myers Squibb Announces Phase 3 ALOFT-IPF Trial Evaluating Admilparant In Adults With Idiopathic Pulmonary Fibrosis Met Primary Endpoint

BRIEF-Bristol Myers Squibb Announces Phase 3 ALOFT-IPF Trial Evaluating Admilparant In Adults With Idiopathic Pulmonary Fibrosis Met Primary Endpoint

- Bristol-Myers Squibb Company BMY.N:

  • BRISTOL MYERS SQUIBB ANNOUNCES PHASE 3 ALOFT-IPF TRIAL EVALUATING ADMILPARANT IN ADULTS WITH IDIOPATHIC PULMONARY FIBROSIS MET PRIMARY ENDPOINT

  • BRISTOL-MYERS SQUIBB COMPANY - ADMILPARANT 60 MG DOSE SHOWS STATISTICALLY SIGNIFICANT FVC IMPROVEMENT AT WEEK 52 VERSUS PLACEBO

  • BRISTOL-MYERS SQUIBB COMPANY - ADMILPARANT DEMONSTRATES FAVORABLE SAFETY AND TOLERABILITY PROFILE

  • BRISTOL-MYERS SQUIBB COMPANY - ADMILPARANT 120 MG DOSE SLOWED FVC DECLINE BUT NOT STATISTICALLY SIGNIFICANT

  • BRISTOL-MYERS SQUIBB COMPANY - ADMILPARANT PHASE 3 ALOFT-PPF TRIAL TOPLINE RESULTS EXPECTED EARLY 2027

Source text: ID:nBw6Hsh6na

Further company coverage: BMY.N


((Reuters.Briefs@thomsonreuters.com;))

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