Trial Profile

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

Status: Not yet recruiting

Phase of Trial: Phase I

Latest Information Update: 29 Apr 2026

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At a glance

Drugs Navlimetostat (Primary)
Indications Adenocarcinoma; Mesothelioma; Neurilemmoma; Non-small cell lung cancer; Pancreatic cancer; Solid tumours
Focus Adverse reactions; Pharmacokinetics
Sponsors Bristol-Myers Squibb

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