A Dose Escalation and Combination Immunotherapy Study to Evaluate BMS-986226 Alone or in Combination With Nivolumab or Ipilimumab in Patients With Advanced Solid Tumors
Part of paid clinical trials in Boston, Massachusetts.
- Sponsor
- Bristol-Myers Squibb
- Study ID
- NCT03251924
- Phase
- PHASE1/PHASE2
- Status
- Terminated
Conditions
- Cancer
- Malignancy
- Neoplasm
- Tumors
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- BMS-986226 — DRUGspecified dose on specified days
- Nivolumab — BIOLOGICALspecified dose on specified days
- Ipilimumab — BIOLOGICALspecified dose on specified days
- Tetanus Vaccine — BIOLOGICALspecified dose on specified days
Study Details
The purpose of this study is to investigate BMS-986226 administered alone or in combination with nivolumab or ipilimumab.
Key Dates
- Start date
- Sep 1, 2017
- Status verified
- Jan 2023
- Primary completion
- Dec 20, 2021
- Completion
- Dec 20, 2021
Study Design
- Enrollment
- 80 participants (actual)
- Allocation
- NON_RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: BMS-986226administered intravenously
- Experimental: BMS-986226 and Nivolumabadministered intravenously
- Experimental: BMS-986226 and Ipilimumabadministered intravenously
Primary Outcome Measure
The Number of Participants Experiencing Adverse Events (AEs) [ Time Frame: From first dose up to 100 days post last dose, up to approximately 31 months ]
Locations (5)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Local Institution - 0005 | Boston | Massachusetts | 02215 | - |
| Local Institution - 0012 | St Louis | Missouri | 63110 | - |
| Local Institution - 0002 | Hackensack | New Jersey | 07601 | - |
| Local Institution - 0001 | Philadelphia | Pennsylvania | 19111 | - |
| Local Institution - 0004 | Nashville | Tennessee | 37203 | - |
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