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A Study to Evaluate the Efficacy, Safety, and Tolerability of BMS-986278 in Participants With Progressive Pulmonary Fibrosis

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A Multicenter, Randomized, Double-blind, Placebo-controlled, Phase 3 Study to Evaluate the Efficacy, Safety, and Tolerability of BMS-986278 in Participants with Progressive Pulmonary Fibrosis (Protocol # IM0271015 )(NCT06025578)

The purpose of this study is to evaluate the efficacy, safety, and tolerability of BMS-986278 in Participants with Progressive Pulmonary Fibrosis.

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Contact

Clinical Trials Office at [email protected] or (203) 358-8879.

Principal Investigator(s)

Caroline Gulati, MD

Sponsor(s)

Bristol-Myers Squibb

Location

SHMG- Pulmonary Associates
29 Hospital Plaza
Stamford, CT 06902

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