Overview
An Investigational Study of Immunotherapy Combinations in Participants With Solid Cancers That Are Advanced or Have Spread
Status:
Recruiting
Recruiting
Trial end date:
2024-07-01
2024-07-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of this study is to investigate safety and anti-tumor activity of relatlimab combination therapy in solid cancers that are advanced or have spreadPhase:
Phase 1/Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Bristol-Myers SquibbTreatments:
Antibodies, Monoclonal
Ipilimumab
Linrodostat
Nivolumab
Criteria
For more information regarding Bristol-Myers Squibb Clinical Trial participation, pleasevisit www.BMSStudyConnect.com
Inclusion Criteria:
- Histologic or cytologic confirmation of an incurable solid malignancy that is advanced
(metastatic and/or unresectable), with measurable disease per RECIST v1.1
- Available tumor tissue for biomarker analysis
- Eastern Cooperative Oncology Group Performance Status (ECOG) status of 0 or 1
Exclusion Criteria:
- Participants with known or suspected uncontrolled CNS metastases or with the CNS as
the only site of active disease
- Participants with a history of interstitial lung disease (ILD) / pneumonitis
- Prior malignancy active within the previous 3 years except for locally curable cancers
that have been cured, such as basal or squamous cell skin cancer
Other protocol defined inclusion/exclusion criteria could apply