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A Phase 1 Study of Navlimetostat Tablet Formulations

NCT07544628

This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .

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

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Healthy Participants

Eligibility basics and study details

Study type
Interventional
Phase
Phase 1
Ages
18 to 55 years
Sex
Female
Healthy volunteers
Accepted
Sponsor
Bristol-Myers Squibb
Last updated on ClinicalTrials.gov
October 7, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Georgia · 1

  • CenExel iResearch - Decatur · Decatur, GA

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.