Antifibrotic Therapy Decision-Making in Pulmonary Fibrosis
← catalyst calendarNCT07722507 · readout in 285 d
Sponsored by Bristol-Myers Squibb (industry) · BMY — their whole pipeline →.
Phase
—
Status
Not yet recruiting
Study type
Observational
Enrollment
40estimated
Sites
1
Country
Japan
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| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2026-08-01 | estimated | When the study began enrolling |
| Primary completion | 2027-05-31 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2027-05-31 | estimated | The whole study's end, after follow-up |
| First posted | 2026-07-23 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-07-23 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Conditions
- Pulmonary Fibrosis
- Idiopathic Pulmonary Fibrosis
- Progressive Pulmonary Fibrosis
Intervention
- Drug: Antifibrotic therapy — also filed as Antifibrotic therapies include pirfenidone, nintedanib or nerandomilast.
Primary outcome
what the primary-completion date above is the date OFParticipant reported decision-making process for antifibrotic therapy persistence or discontinuation when considering the impact of tolerability and adverse events collected via semi-structured qualitative participant interviews
measured Day 1
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