Pan Tumor Rollover Study
← catalyst calendarNCT03899155 · 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| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2019-08-09 | actual | When the study began enrolling |
| Primary completion | 2029-08-25 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2029-08-25 | estimated | The whole study's end, after follow-up |
| First posted | 2019-04-02 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-07-29 | actual | The 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 OFIncidence 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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