Bristol admilparant Phase 3 IPF win lifts Contineum pre-market on LPA1 readthrough
BMS admilparant Phase 3 IPF win lifts Contineum 21% pre-market on LPA1 readthrough
- Bristol Myers Squibb announced Monday that Phase 3 ALOFT-IPF of LPA1 antagonist admilparant met its primary FVC endpoint.
- The 60 mg dose showed statistically significant FVC improvement versus placebo at week 52; 120 mg slowed decline without significance.
- Safety was well tolerated with adverse-event discontinuations similar to placebo, easing prior liver-toxicity class concerns.
- Contineum's lead PIPE-791 is a once-daily LPA1 antagonist in Phase 2 for idiopathic pulmonary fibrosis, making this a class-validating readthrough.
- Analysts including Stifel had flagged the BMS readout as a potential derisking event for Contineum's IPF program.
- The news hit around 5:55 AM ET per Reuters, driving the pre-market gap from Friday's $13.38 close.
- No Contineum press release or SEC filing appeared; Finviz listed no ticker-specific headline since the prior close.
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