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A Study to Assess Safety, Tolerability and Drug Levels of Navlimetostat (BMS-986504) in Participants With Advanced Solid Tumors

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NCT07077434 · readout in 153 d

Sponsored by Bristol-Myers Squibb (industry) · BMY — their whole pipeline →.

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
32estimated
Sites
12
Countries
China, Japan

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-10-15actualWhen the study began enrolling
Primary completion2027-01-19estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-01-19estimatedThe whole study's end, after follow-up
First posted2025-07-22actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-06-03actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Advanced Solid Tumors

Intervention

  • Drug: BMS-986504 — also filed as MRTX1719

Primary outcomes

what the primary-completion date above is the date OF
Maximum Plasma Concentration (Cmax) of BMS-986504
measured Up to approximately Day 64
Time to Reach Maximum Plasma Concentration (Tmax) of BMS-986504
measured Up to approximately Day 64
Area Under Curve (AUC) of BMS-986504
measured Up to approximately Day 64
Mean Elimination Half-life (T-HALF) of BMS-986504
measured Up to approximately Day 64
Apparent Total Body Clearance (CLT/F) of BMS-986504
measured Up to approximately Day 64
Apparent Volume of Distribution During the Terminal Phase (Vz/F) of BMS-986504
measured Up to approximately Day 64

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