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Long-term Extension Study to Evaluate Safety and Tolerability of Admilparant in Participants With Pulmonary Fibrosis

← catalyst calendar

NCT07441408 · readout in 1,191 d

Sponsored by Bristol-Myers Squibb (industry) · BMY — their whole pipeline →.

Phase
Phase 3
Status
Not yet recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
2,380estimated
Sites
275
Countries
Argentina, Australia, Belgium +24

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2026-12-16estimatedWhen the study began enrolling
Primary completion2029-11-22estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2030-03-30estimatedThe whole study's end, after follow-up
First posted2026-03-02actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-14actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Pulmonary Fibrosis

Intervention

  • Drug: BMS-986278 — also filed as Admilparant

Primary outcomes

what the primary-completion date above is the date OF
Number of Participants With Treatment Emergent Adverse Events (TEAEs)
measured Up to Week 100
Number of Participants With Serious Adverse Events (SAEs)
measured Up to Week 100
Number of Participants With AEs leading to Discontinuation
measured Up to Week 100
Number of Participants With AEs leading to Deaths
measured Up to Week 100
Number of Participants With Clinically Significant Laboraty Abnormalities
measured Up to Week 100
Number of Participants With Clinically Significant Electocardiogram (ECG) Abnormalities
measured Up to Week 100
Number of Participants With Clinically Significant Vital Sign Abnormalities
measured Up to Week 100

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