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A Study of BMS-986484 Alone and Combination Therapy in Participants With Advanced Solid Tumors

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NCT06544655 · readout in 420 d

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

Phase
Phase 1
Status
Active, not recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
213estimated
Sites
9
Countries
Australia, Canada, United States

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
Start2024-10-10actualWhen the study began enrolling
Primary completion2027-10-14estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-10-14estimatedThe whole study's end, after follow-up
First posted2024-08-09actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-04-17actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Advanced Solid Tumors

Interventions

  • Drug: BMS-986484
  • Biological: Nivolumab — also filed as Opdivo
  • Drug: Oxaliplatin
  • Drug: Capecitabine
  • Drug: Fluorouracil
  • Drug: Calcium folinate

Primary outcomes

what the primary-completion date above is the date OF
Incidence of adverse events (AEs)
measured Up to approximately 2 years
Incidence of serious adverse events (SAEs)
measured Up to approximately 2 years
Incidence of AEs meeting protocol defined dose-limiting toxicity (DLT) criteria
measured Up to approximately 28 days
Incidence of AEs leading to discontinuation
measured Up to approximately 2 years
Incidence of AEs leading to death
measured Up to approximately 2 years

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