Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
The purpose of this study is to evaluate the treatment of solid tumors with various immunotherapy combinations. The treatment will be determined based upon a broad biomarker assessment.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Arm B | Experimental | Combination therapy determined by biomarker assessment |
|
| Arm C | Experimental | Combination therapy determined by biomarker assessment |
|
| Arm D | Experimental | Combination therapy determined by biomarker assessment |
|
| Arm F | Experimental | Combination therapy determined by biomarker assessment |
|
| Arm G | Experimental | Combination therapy determined by biomarker assessment |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Nivolumab | Biological | Specified dose on specified day |
|
| Measure | Description | Time Frame |
|---|---|---|
| Number of participants with qualified tumor biopsy specimen at baseline | An adequate quality tumor biopsy providing sufficient information prior to choosing a combination immunotherapy/Stereotactic Body Radiation Therapy (SBRT) | Up to 28 days |
| Measure | Description | Time Frame |
|---|---|---|
| Percent of change from baseline in histopathologic features | Up to 4 years | |
| Percent of change from baseline in biomarker expression patterns | Up to 4 years | |
| Number of Adverse Events (AEs) |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Other protocol defined inclusion/exclusion criteria could apply
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Bristol-Myers Squibb | Bristol-Myers Squibb | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Local Institution - 0001 | Chicago | Illinois | 60637 | United States | ||
| University of Chicago |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 40389374 | Derived | Luke JJ, Bever K, Hodi FS, Taube J, Massey A, Yao D, Neely J, Tam R, Lee G, Gupta A, Dutta S, Szabo P, Bao R, Reilly T. Rationale and feasibility of a rapid integral biomarker program that informs immune-oncology clinical trials: the ADVISE trial. J Immunother Cancer. 2025 May 19;13(5):e011170. doi: 10.1136/jitc-2024-011170. |
| Label | URL |
|---|---|
| BMS Clinical Trial Information | View source |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Relatlimab | Biological | Specified dose on specified day |
|
|
| Cabiralizumab | Biological | Specified dose on specified day |
|
|
| Ipilimumab | Biological | Specified dose on specified day |
|
|
| IDO1 Inhibitor | Drug | Specified dose on specified day |
|
|
| Radiation Therapy | Radiation | Specified dose on specified day |
|
| Up to 4 years |
| Number of Serious Adverse Events (SAEs) | Up to 4 years |
| Number of Laboratory Abnormalities | Any laboratory test result that is clinically significant or meets the definition of an SAE, requires the participant to have study treatment discontinued, or receive specific corrective therapy | Up to 4 years |
| Number of Adverse Events(AEs) leadind to discontinutaion | Number of Adverse Events leadind to discontinutaion | up to 4 years |
| Number of Deaths | up to 4 years |
| Chicago |
| Illinois |
| 60637 |
| United States |
| Local Institution - 0002 | Baltimore | Maryland | 21287 | United States |
| Local Institution - 0003 | Pittsburgh | Pennsylvania | 15232 | United States |
| BMS Clinical Trial Patient Recruiting | View source |
| FDA Safety Alerts and Recalls | View source |
| ID | Term |
|---|---|
| D000077594 | Nivolumab |
| C000721227 | relatlimab |
| C000722457 | cabiralizumab |
| D000074324 | Ipilimumab |
| C000723356 | IDO-1 inhibitor LY3381916 |
| C000630574 | linrodostat |
| D011878 | Radiotherapy |
| ID | Term |
|---|---|
| D061067 | Antibodies, Monoclonal, Humanized |
| D000911 | Antibodies, Monoclonal |
| D000906 | Antibodies |
| D007136 | Immunoglobulins |
| D007162 | Immunoproteins |
| D001798 | Blood Proteins |
| D011506 | Proteins |
| D000602 | Amino Acids, Peptides, and Proteins |
| D012712 | Serum Globulins |
| D005916 | Globulins |
| D013812 | Therapeutics |
Not provided
Not provided