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NOT YET RECRUITING
NCT07544628
PHASE1

A Phase 1 Study of Navlimetostat Tablet Formulations

Sponsor: Bristol-Myers Squibb

View on ClinicalTrials.gov

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

Interventions

DRUG

Navlimetostat

Specified dose on specified days