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[Baltimore] => https://www.survivornet.com/baltimore/
[Charlotte] => https://www.survivornet.com/charlotte/
[Cleveland] => https://www.survivornet.com/cleveland/
[Columbus] => https://www.survivornet.com/columbus/
[Dallas / Ft. Worth] => https://www.survivornet.com/dallas-ftworth/
[Denver] => https://www.survivornet.com/denver/
[Detroit] => https://www.survivornet.com/detroit/
[Indianapolis] => https://www.survivornet.com/indianapolis-ovarian-cancer/
[Louisville] => https://www.survivornet.com/louisville/
[Memphis] => https://www.survivornet.com/memphis/
[Minneapolis] => https://www.survivornet.com/minneapolis/
[Nashville] => https://www.survivornet.com/nashville/
[Phoenix] => https://www.survivornet.com/phoenix/
[Portland] => https://www.survivornet.com/portland/
[Salt Lake City] => https://www.survivornet.com/salt-lake-city/
[San Antonio] => https://www.survivornet.com/san-antonio/
[San Diego] => https://www.survivornet.com/san-diego/
[San Francisco] => https://www.survivornet.com/san-francisco/
[San Jose] => https://www.survivornet.com/san-jose/
[Seattle] => https://www.survivornet.com/seattle/
) [Multiple Myeloma] => Array
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[Miami] => https://www.survivornet.com/miami-florida-multiple-myeloma-treatment/
[Phoenix] => https://www.survivornet.com/phoenix-arizona-multiple-myeloma-treatment/
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[Mountain States] => https://www.survivornet.com/glioma-mountain-states/
[Southeast] => https://www.survivornet.com/southeast/
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[Miami] => https://www.survivornet.com/miami-advanced-prostate-cancer/
[Philadelphia] => https://www.survivornet.com/philadelphia/
) [Non-Hodgkin Lymphoma] => Array
(
[Houston] => https://www.survivornet.com/houston-advanced-large-b-cell/
) )
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.
View Eligibility Criteria 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
Check Your Eligibility
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There are 8 Locations for this study
Local Institution - 0028 Sioux Falls South Dakota, 57104, United States
Local Institution - 0001 Germantown Tennessee, 38138, United States
Local Institution - 0014 Edmonton Alberta, T6X 1, Canada
Local Institution - 0011 Vancouver British Columbia, V5Z 4, Canada
Local Institution - 0004 Toronto Ontario, M5G 2, Canada
Local Institution - 0005 Montreal Quebec, H2X 3, Canada
Local Institution - 0013 Ottawa , K1H 8, Canada
Local Institution Mexico city Distrito Federal, 06100, Mexico
How clear is this clinincal trial information?
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