Study on BMS-986482 Alone or in Combination for Advanced Solid Tumors
Sponsor: Bristol-Myers Squibb
Sponsor score: 60
ClinicalTrials ID:NCT06697197
This clinical trial is testing the safety and effectiveness of a new drug, BMS-986482, used alone or with other treatments in adults with advanced solid tumors that cannot be surgically removed or have spread to other parts of the body.
Patient Parameters
| Parameter | Options |
|---|
Program Overview
The aim of this study is to evaluate how safe and effective the drug BMS-986482 is when used by itself or with other treatments in patients with advanced solid tumors. These are cancers that have spread or cannot be removed by surgery.
Eligibility Criteria
Inclusion Criteria
- Must have a confirmed diagnosis of advanced solid cancer that cannot be removed by surgery or has spread, and must have tried or be unable to try other treatments that could help.
- Must be 18 years or older.
- For Part 1A, participants may have certain types of cancer such as lung, head and neck, colorectal, stomach, bladder, pancreatic, melanoma, or breast cancer.
- For Parts 1B1 and 2B1, participants must have non-small cell lung cancer (NSCLC) and should know the status of certain genetic mutations if possible. They must have had platinum-based chemotherapy and anti-PD-(L)1 therapy if eligible.
- For Parts 1B2, 2B2, and 1C, participants must have certain types of melanoma, but not uveal/ocular melanoma, and must have had at least one prior treatment.
- For Part 1B3, participants must have advanced or metastatic colorectal cancer.
- For Part 2A, participants may have advanced solid tumors like NSCLC, hormone-resistant breast cancer, or pancreatic cancer.
- For Part 2B3, participants must have advanced or metastatic colorectal cancer.
- For Part 1C, a fresh tumor sample must be obtained if possible.
Exclusion Criteria
- History of severe immune-related side effects from previous T-cell or checkpoint inhibitor treatments, unless they are unlikely to happen again with standard treatments.
- Any serious medical condition that could interfere with the study or follow-up, as determined by the study doctor.
- Other specific criteria as defined by the study protocol.
Locations
| FACILITY | ZIP | CITY | STATE |
|---|---|---|---|
| Local Institution - 0005 | 92612 | Irvine | California |
| Local Institution - 0030 | 90025 | Los Angeles | California |
| Local Institution - 0008 | 80045 | Aurora | Colorado |
| John Theurer Cancer Center at Hackensack University Medical Center | 07601 | Hackensack | New Jersey |
| Local Institution - 0007 | 11042 | Lake Success | New York |
| Local Institution - 0011 | 28204 | Charlotte | North Carolina |
| Local Institution - 0010 | 98109 | Seattle | Washington |
Get This Program In Your Inbox
Receive detailed information about this treatment opportunity to review with your healthcare provider.
