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[Cleveland] => https://www.survivornet.com/cleveland/
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A Study to Evaluate Whether Participants With Melanoma Prefer Subcutaneous vs Intravenous Administration of Nivolumab and Nivolumab + Relatlimab Fixed-dose Combinations Summary The purpose of this study is to assess the patient's preference for nivolumab subcutaneous (SC) or nivolumab + relatlimab fixed-dose combination (FDC) SC and provide patient experience data by route of administration. This study will also generate safety data which will further characterize the safety profile of patients switching the route of administration from intravenous (IV) to SC.
View Eligibility Criteria Eligibility Criteria Inclusion Criteria: Must have either metastatic melanoma and have not had previous treatment for their cancer, or resected melanoma and have had the cancer removed fully with surgery no later than 12 weeks before the start of treatment and confirmed free of disease Must have a low level of disability and cancer that is considered advanced for metastatic melanoma and at risk for becoming advanced (intermediate) or advanced for resected melanoma Exclusion Criteria: Must not have any brain cancer/disease treated with radiation , any cancer in the eyes or mucous membranes (cells that cover inside surface of parts of the body and keep it moist), any autoimmune disease, or any condition that is being treated with steroids for inflammation (corticosteroids) or medication to decrease the body's immune system response (immunosuppressive drugs) Other protocol-defined inclusion/exclusion criteria apply.
Check Your Eligibility
Let’s see if you might be eligible for this study.
What is your age and gender ?
There are 35 Locations for this study
Alaska Oncology & Hematology, LLC Anchorage Alaska, 99508, United States
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Mayo Clinic Hospital - Phoenix Phoenix Arizona, 85054, United States
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University of California, San Francisco, Medical Center at Mount Zion San Francisco California, 94115, United States
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Local Institution - 0034 Atlanta Georgia, 30342, United States
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Saint Elizabeth Healthcare Edgewood Kentucky, 41017, United States
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University of New Mexico Cancer Center Albuquerque New Mexico, 87106, United States
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Icahn School of Medicine at Mount Sinai (ISMMS) - The Derald H. Ruttenberg Treatment Center New York New York, 10029, United States
Swedish Cancer Institute Seattle Washington, 98104, United States
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Local Institution - 0024 Cipolletti R, 8324, Argentina
Local Institution - 0002 Viedma R, R8500, Argentina
Local Institution - 0001 Rosario S, 2000, Argentina
Local Institution - 0015 Las Condes Santiago, 83310, Chile
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Servicios Medicos e Investigacion Biocenter SpA Concepcion , 40701, Chile
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Local Institution - 0016 Las Condes , 75500, Chile
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Bioclinic of Thessaloniki Thessaloniki B, 546 2, Greece
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Local Institution - 0014 Athens I, 115 2, Greece
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Local Institution - 0031 Kifisia I, 145 6, Greece
Athens Medical Center Marousi I, 151 2, Greece
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Metropolitan General Hospital Holargos, Athens , 155 6, Greece
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Metropolitan Hospital, Department of Oncology Peiraias , 185 4, Greece
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Local Institution - 0033 Thessaloniki , 564 2, Greece
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ASST Papa Giovanni XXIII Bergamo BG, 24127, Italy
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Local Institution - 0035 Meldola FC, 47014, Italy
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Istituto Europeo di Oncologia Milan MI, 20141, Italy
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Local Institution - 0012 Padova PD, 35128, Italy
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Istituto Nazionale Tumori Regina Elena Roma RM, 00144, Italy
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Azienda Ospedaliero Universitaria Città della Salute e della Scienza di Torino Torino TO, 10126, Italy
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Local Institution - 0026 Napoli , 80131, Italy
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Hospital de la Santa Creu i Sant Pau Barcelona B, 08025, Spain
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Local Institution - 0022 Barcelona B, 08908, Spain
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Hospital Universitario Virgen Arrixaca Cartagena MU, 30120, Spain
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Local Institution - 0020 Badalona , 08916, Spain
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Local Institution - 0027 Cantabria , 39008, Spain
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Hospital San Pedro de Alcántara San Pedro Alcántara, Málaga , 10002, Spain
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Hospital Universitario Virgen del Rocío Sevilla , 41013, Spain
More Info How clear is this clinincal trial information?
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