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A Phase 1 Study of Navlimetostat Tablet Formulations
Sponsor: Bristol-Myers Squibb
Summary
This study aims to compare the PK of Navlimetostat after administration of a wet-granulation tablet versus the dry-granulation tablet formulation in healthy adult female
Official 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
Key Details
Gender
FEMALE
Age Range
18 Years - 55 Years
Study Type
INTERVENTIONAL
Enrollment
64
Start Date
2026-04-30
Completion Date
2026-10-15
Last Updated
2026-04-22
Healthy Volunteers
Yes
Conditions
Interventions
Navlimetostat
Specified dose on specified days