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A Study to Assess the Effect of Food on the Drug Levels of Admilparant

← catalyst calendar

NCT07225647

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

Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
56actual
Sites
2
Country
United States

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
Start2025-11-07actualWhen the study began enrolling
Primary completion2026-01-05actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-01-05actualThe whole study's end, after follow-up
First posted2025-11-10actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-01-14actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Healthy Participants

Intervention

  • Drug: Admilparant

Primary outcomes

what the primary-completion date above is the date OF
Maximum observed plasma concentration (Cmax)
measured Up to 13 days
Area under the concentration-time curve from time zero to time of last quantifiable concentration (AUC(0-T))
measured Up to 13 days
Area under the concentration-time curve from time zero extrapolated to infinite time (AUC(INF))
measured Up to 13 days

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