Clinical trial
A Phase 1, Open-label, Randomized, 2-Treatment, 2-Period, Crossover Study to Assess the Bioequivalence of Navlimetostat Wet-Granulation Tablet Versus the Dry-Granulation Tablet Formulation in Healthy Adult Female (as Assigned at Birth) Participants Who Are Individuals Not of Childbearing Potential
NCT07544628 is registered in ClinicalTrials.gov with Bristol-Myers Squibb as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Phase 1, Open-label, Randomized, 2-Treatment, 2-Period, Crossover Study to Assess the Bioequivalence of Navlimetostat Wet-Granulation Tablet Versus the Dry-Granulation Tablet Formulation in Healthy Adult Female (as Assigned at Birth) Participants Who Are Individuals Not of Childbearing Potential
- Lead sponsor
- Bristol-Myers Squibb
- Phase
- Phase 1
- Overall status
- Recruiting
- Start date
- April 27, 2026
- Completion date
- November 2, 2026
- Enrollment
- 64 (estimated)
- Sites
- 4
Conditions
As the registry lists them; a condition with its own page is linked.
healthy participants