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A Study to Evaluate the Mass Balance, Metabolism, Elimination, and Drug Levels of [14C]-BMS-986504 (MRTX1719) in Participants With Advanced Solid Tumors With Homozygous Methylthioadenosine Phosphorylase Deletion

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NCT06672523 · readout in 432 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
8estimated
Sites
3
Countries
Hungary, Spain

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
Start2025-03-24actualWhen the study began enrolling
Primary completion2027-10-25estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-10-25estimatedThe whole study's end, after follow-up
First posted2024-11-04actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-06-08actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Advanced Solid Tumors With Homozygous MTAP Deletion

Interventions

  • Drug: BMS-986504
  • Drug: [14C]-BMS-986504

Primary outcomes

what the primary-completion date above is the date OF
Maximum observed concentration (Cmax)
measured Up to 2 weeks
Time of maximum observed drug concentration (Tmax)
measured Up to 2 weeks
Area under the concentration-time curve from time zero to the time of the last quantifiable concentration (AUC(0-T))
measured Up to 2 weeks
Area under the concentration-time curve from time zero extrapolated to infinite time (AUC(INF))
measured Up to 2 weeks
Terminal elimination half-life (T-HALF)
measured Up to 2 weeks
Apparent total body clearance (CLT/F)
measured Up to 2 weeks
Apparent volume of distribution during the terminal phase (Vz/F)
measured Up to 2 weeks
Percentage of estimated part for the calculation of AUC(INF) (%AUC(INF))
measured Up to 2 weeks
Blood-to-plasma total radioactivity (TRA) ratio
measured Up to 2 weeks
Total amount of administered dose recovered in urine (UR)
measured Up to 2 weeks
Percent of administered dose recovered in urine (%UR)
measured Up to 2 weeks
Renal clearance (CLR) in urine
measured Up to 2 weeks
Total radioactivity in UR
measured Up to 2 weeks
Total radioactivity in %UR
measured Up to 2 weeks
Total radioactivity in total amount of administered dose recovered in feces (FR)
measured Up to 2 weeks
Total radioactivity in percent of administered dose recovered in feces (%FR)
measured Up to 2 weeks
Total amount of radioactivity recovered (Rtotal)
measured Up to 2 weeks
Total percent of radioactivity recovered (%TOTAL)
measured Up to 2 weeks
TRA amount recovered and fraction of the radioactive dose in vomit if applicable
measured Up to 2 weeks

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