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Spots Global Cancer Trial Database for An Investigational Immuno-therapy Study to Investigate the Safety and Effectiveness of Nivolumab, and Nivolumab Combination Therapy in Virus-associated Tumors

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Trial Identification

Brief Title: An Investigational Immuno-therapy Study to Investigate the Safety and Effectiveness of Nivolumab, and Nivolumab Combination Therapy in Virus-associated Tumors

Official Title: Non-Comparative, Open-Label, Multiple Cohort, Phase 1/2 Study of Nivolumab Monotherapy and Nivolumab Combination Therapy in Subjects With Virus-Positive and Virus-Negative Solid Tumors

Study ID: NCT02488759

Study Description

Brief Summary: The purpose of this study to investigate the safety and effectiveness of nivolumab, and nivolumab combination therapy, to treat patients who have virus-associated tumors. Certain viruses have been known to play a role in tumor formation and growth. This study will investigate the effects of the study drugs, in patients who have the following types of tumors: * Anal canal cancer-No longer enrolling this tumor type * Cervical cancer * Epstein Barr Virus (EBV) positive gastric cancer-No longer enrolling this tumor type * Merkel Cell Cancer * Penile cancer-No longer enrolling this tumor type * Vaginal and vulvar cancer-No longer enrolling this tumor type * Nasopharyngeal Cancer - No longer enrolling this tumor type * Head and Neck Cancer - No longer enrolling this tumor type

Detailed Description:

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Local Institution - 0033, Tampa, Florida, United States

Local Institution - 0003, Atlanta, Georgia, United States

Local Institution - 0023, Lutherville, Maryland, United States

Local Institution - 0002, Boston, Massachusetts, United States

Local Institution - 0019, Boston, Massachusetts, United States

Local Institution - 0020, Boston, Massachusetts, United States

Local Institution - 0035, Ann Arbor, Michigan, United States

Local Institution - 0036, New York, New York, United States

Local Institution - 0022, Charlotte, North Carolina, United States

Local Institution - 0005, Oklahoma City, Oklahoma, United States

Local Institution - 0004, Portland, Oregon, United States

Local Institution - 0029, Pittsburgh, Pennsylvania, United States

Local Institution - 0001, Sioux Falls, South Dakota, United States

Local Institution - 0021, Seattle, Washington, United States

Local Institution - 0012, Brussels, , Belgium

Local Institution - 0014, Brussels, , Belgium

Local Institution - 0013, Bruxelles, , Belgium

Local Institution - 0031, Marseille Cedex 9, , France

Local Institution - 0038, Paris, , France

Local Institution - 0032, Toulouse Cedex 9, , France

Local Institution - 0030, Vlllejuif, , France

Local Institution - 0027, Essen, , Germany

Local Institution - 0028, Heilbronn, , Germany

Local Institution - 0039, Kashiwa-shi, Chiba, Japan

Local Institution - 0040, Chuo-ku, Tokyo, Japan

Local Institution - 0041, Koto-ku, Tokyo, Japan

Local Institution - 0024, Seoul, , Korea, Republic of

Local Institution - 0056, Mexico City, Distrito Federal, Mexico

Local Institution, Oaxaca de Juarez, Oaxaca, Mexico

Local Institution - 0046, Merida, Yucatan, Mexico

Local Institution - 0011, Amsterdam, , Netherlands

Local Institution - 0034, Utrecht, , Netherlands

Local Institution - 0018, Barcelona, , Spain

Local Institution - 0017, Madrid, , Spain

Local Institution - 0016, Navarra, , Spain

Local Institution - 0037, Tainan, , Taiwan

Local Institution - 0026, Taipei, , Taiwan

Local Institution - 0006, Glasgow, Lanarkshire, United Kingdom

Local Institution - 0010, Birmingham, West Midlands, United Kingdom

Local Institution - 0008, London, , 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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