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Spots Global Cancer Trial Database for An Investigational Immuno-therapy Safety and Effectiveness Study of Nivolumab in Combination With Brentuximab Vedotin to Treat Non-Hodgkin Lymphomas

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Trial Identification

Brief Title: An Investigational Immuno-therapy Safety and Effectiveness Study of Nivolumab in Combination With Brentuximab Vedotin to Treat Non-Hodgkin Lymphomas

Official Title: A Phase I/ II Study to Evaluate the Safety and Preliminary Efficacy of Nivolumab in Combination With Brentuximab Vedotin in Subjects With Relapsed Refractory Non Hodgkin Lymphomas With CD30 Expression (CheckMate 436: CHECKpoint Pathway and Nivolumab Clinical Trial Evaluation 436)

Study ID: NCT02581631

Study Description

Brief Summary: The purpose of this study is to determine whether Nivolumab, in combination with brentuximab vedotin, is safe and effective in patients with certain subtypes of non-Hodgkin's lymphomas with CD30 expression that have not responded to treatment or have come back. The subtypes we are studying are Diffuse Large B-Cell Lymphoma (DLBCL), Peripheral T-Cell Lymphoma (PTCL), Cutaneous T-Cell Lymphoma (CTCL), Primary Mediastinal Large B-Cell Lymphoma (PMBL) and Mediastinal Gray Zone Lymphoma (MGZL).

Detailed Description:

Keywords

Eligibility

Minimum Age: 15 Years

Eligible Ages: CHILD, ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Local Institution - 0017, Birmingham, Alabama, United States

University Of Miami Sylvester Comprehensive Cancer Center, Miami, Florida, United States

Local Institution - 0012, Tampa, Florida, United States

Winship Cancer Institute., Atlanta, Georgia, United States

University Of Chicago, Chicago, Illinois, United States

Mayo Clinic, Rochester, Minnesota, United States

Washington University School Of Medicine, Saint Louis, Missouri, United States

Local Institution - 0003, New York, New York, United States

Local Institution - 0010, New York, New York, United States

University Of Rochester, Rochester, New York, United States

Levine Cancer Institute, Charlotte, North Carolina, United States

The Ohio State University Comprehensive Cancer Center, Columbus, Ohio, United States

Stephenson Cancer Center, Oklahoma City, Oklahoma, United States

Providence Portland Medical Center, Portland, Oregon, United States

Bon Secours-St Francis Hosp, Greenville, South Carolina, United States

University of Washington - Seattle Cancer Care Alliance, Seattle, Washington, United States

BC Cancer Agency - Vancouver Centre, Vancouver, British Columbia, Canada

Local Institution - 0011, Toronto, Ontario, Canada

Jewish General Hospital, Montreal, Quebec, Canada

Hopital Saint Louis, Paris, , France

Local Institution - 0020, Pierre Benite Cedex, , France

Local Institution - 0018, Bergamo, , Italy

Local Institution - 0024, Bologna, , Italy

Istituto Clinico Humanitas, Rozzano (milano), , Italy

Local Institution - 0027, Hospitalet de Llobregat - Barcelona, , Spain

Churchill Hospital, Oxford, Oxfordshire, United Kingdom

Royal Marsden Hospital, Sutton, Surrey, United Kingdom

Contact Details

Name: Bristol-Myers Squibb

Affiliation: Bristol-Myers Squibb

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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