A Study of BMS-986360/CC-90001 Alone and in Combination With Chemotherapy or Nivolumab in Advanced Solid Tumors
Part of paid clinical trials in Los Angeles, California.
- Sponsor
- Bristol-Myers Squibb
- Study ID
- NCT05625412
- Phase
- PHASE1
- Status
- Completed
Conditions
- Advanced Solid Tumors
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- BMS-986360 — DRUGSpecified dose on specified days
- Docetaxel — DRUGSpecified dose on specified days
- Nivolumab — DRUGSpecified dose on specified days
- Capecitabine — DRUGSpecified dose on specified days
Study Details
The aim of this study is to assess the safety and tolerability of BMS-986360 as monotherapy and in combination with chemotherapy or nivolumab in participants with advanced solid tumors.
Key Dates
- Start date
- Dec 9, 2022
- Status verified
- Jun 2025
- Primary completion
- May 12, 2025
- Completion
- May 12, 2025
Study Design
- Enrollment
- 70 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: BMS-986360
- Experimental: BMS-986360 + Docetaxel
- Experimental: BMS-986360 + Nivolumab
- Experimental: BMS-986360 + Capecitabine
Primary Outcome Measure
Number of participants with Adverse Events (AEs) [ Time Frame: Up to approximately 2 years ]
Locations (8)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Local Institution - 0029 | Los Angeles | California | 90025 | - |
| Local Institution - 0051 | Los Angeles | California | 90067 | - |
| Local Institution - 0026 | New Orleans | Louisiana | 70121 | - |
| Local Institution - 0001 | Hackensack | New Jersey | 07601 | - |
| Local Institution - 0018 | Huntersville | North Carolina | 28078 | - |
| Local Institution - 0028 | Nashville | Tennessee | 37203 | - |
| Local Institution - 0027 | San Antonio | Texas | 78229 | - |
| Local Institution - 0046 | West Valley City | Utah | 84119 | - |
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