Kidney Cancer Clinical Trial
Study of BMS-986315 Alone and in Combination With Nivolumab or Cetuximab in Participants With Advanced Solid Tumors
Summary
The purpose of this study is to evaluate BMS-986315 alone and in combination with nivolumab or cetuximab in participants with advanced solid tumors.
Eligibility Criteria
Inclusion Criteria:
Participants must have histologic confirmation of advanced (metastatic, recurrent, and/or unresectable) squamous cell carcinoma of the head and neck (SCCHN), nonsmall cell lung cancer (NSCLC), or renal cell cancer (RCC) with measurable disease per RECIST 1.1
Participants expected to have received standard of care therapies including an available PD-(L)1 inhibitor
Eastern cooperative oncology group performance status of 0 or 1
Women of childbearing potential must agree to follow methods of contraception
Exclusion Criteria:
Participants with active, known or suspected autoimmune disease
Participants with a condition requiring systemic treatment with either corticosteroids or other immunosuppressive medications
Uncontrolled or significant cardiovascular disease
History of or with active interstitial lung disease or pulmonary fibrosis
Prior participation in anti-natural killer cell receptor (anti-NKG2A) clinical study
History of allergy or hypersensitivity to study drug components
Other protocol-defined inclusion/exclusion criteria apply
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There are 8 Locations for this study
Sioux Falls South Dakota, 57104, United States
Germantown Tennessee, 38138, United States
Edmonton Alberta, T6X 1, Canada
Vancouver British Columbia, V5Z 4, Canada
Toronto Ontario, M5G 2, Canada
Montreal Quebec, H2X 3, Canada
Ottawa , K1H 8, Canada
Mexico city Distrito Federal, 06100, Mexico
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