drugset / Trial / NCT04308681

A Study Measuring the Effectiveness, Safety, and Tolerability of BMS-986278 in Participants With Lung Fibrosis

NCT04308681

Phase 2 Completed 403 enrolled Bristol-Myers Squibb
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to provide an initial evaluation of the effectiveness of BMS-986278 in participants with lung fibrosis, to demonstrate the safety of BMS-986278, and provide information on the drug levels of BMS-986278 in these participants.

Timeline

Start
2020-07-29
Primary completion
2022-08-04
Completion
2023-09-22

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Admilparant Small molecule 30 mg Oral
Subject Admilparant Small molecule 60 mg Oral

Indications