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Pan Tumor Rollover Study

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NCT03899155 · readout in 1,102 d

Sponsored by Bristol-Myers Squibb (industry) · BMY — their whole pipeline →. With Exelixis, Novartis, Clovis Oncology, Inc., Janssen Pharmaceuticals.

Phase
Phase 2
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
1,500estimated
Sites
399
Countries
Argentina, Australia, Austria +35

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
Start2019-08-09actualWhen the study began enrolling
Primary completion2029-08-25estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2029-08-25estimatedThe whole study's end, after follow-up
First posted2019-04-02actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-29actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Cancer

Interventions

  • Drug: Nivolumab — also filed as BMS-936558-01
  • Drug: Ipilimumab
  • Drug: Cabozantinib
  • Drug: Trametinib
  • Drug: Relatlimab — also filed as BMS-986016-01
  • Drug: Nivolumab + Relatlimab — also filed as BMS-986213
  • Drug: Capecitabine
  • Drug: Bevacizumab
  • Drug: Temozolomide
  • Drug: Rucaparib
  • Drug: Daratumumab
  • Drug: Regorafinib
  • Drug: Leucovorin
  • Drug: Fluorouracil
  • Drug: Oxaliplatin
  • Drug: Enzalutamide
  • Drug: Sunitinib
  • Drug: Pemetrexed
  • Drug: Pembrolizumab

Primary outcomes

what the primary-completion date above is the date OF
Incidence of Adverse Events (AEs)
measured From Day 1 up to 135 Days after discontinuation of treatment
Incidence of drug related AEs
measured From Day 1 up to 135 Days after discontinuation of treatment
Incidence of AEs leading to Discontinuation
measured From Day 1 up to 135 Days after discontinuation of treatment
Incidence of Serious Adverse Events (SAEs)
measured From signature of Informed Consent up to 135 Days after discontinuation of treatment
Incidence of Select AEs
measured From Day 1 up to 135 Days after discontinuation of treatment
Incidence of Immune-Mediated AEs
measured From Day 1 up to 135 Days after discontinuation of treatment
Incidence of Death
measured From signature of Informed Consent up to 135 Days after discontinuation of treatment

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