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Spots Global Cancer Trial Database for Study to Explore the Safety, Tolerability and Efficacy of MK-3475 in Combination With INCB024360 in Participants With Selected Cancers

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Trial Identification

Brief Title: Study to Explore the Safety, Tolerability and Efficacy of MK-3475 in Combination With INCB024360 in Participants With Selected Cancers

Official Title: A Phase 1/2 Study Exploring the Safety, Tolerability, and Efficacy of MK-3475 in Combination With INCB024360 in Subjects With Selected Cancers (ECHO-202/KEYNOTE-037)

Study ID: NCT02178722

Interventions

MK-3475
INCB024360

Study Description

Brief Summary: The purpose of this study was to assess the safety, tolerability, and efficacy when combining MK-3475 and INCB024360 in participants with certain cancers. This study was conducted in 2 phases, Phase 1 and Phase 2.

Detailed Description:

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

UC San Diego Moores Cancer Center, La Jolla, California, United States

The Angeles Clinic and Research Institute, Los Angeles, California, United States

US Davis Cancer Center, Sacramento, California, United States

University Of Colorado Cancer Center, Aurora, Colorado, United States

University of Connecticut Health Center Carole And Ray Neag Comprehensive Cancer Center, Farmington, Connecticut, United States

Miami Cancer Institute at Baptist Health, Inc, Miami, Florida, United States

Georgia Cancer Specialists affiliated with Northside Hospital Cancer Institute, Atlanta, Georgia, United States

The University of Chicago Medicine, Chicago, Illinois, United States

St. Francis Cancer Center, Topeka, Kansas, United States

Greater Baltimore Cancer Center, Baltimore, Maryland, United States

St. Agnes Hospital Cancer Institute, Baltimore, Maryland, United States

The Center for Cancer and Blood Disorders (RCCA MD LLC- Maryland Division), Bethesda, Maryland, United States

University of Michigan Hospital and Health Systems, Ann Arbor, Michigan, United States

Health Partners Institute, Saint Louis Park, Minnesota, United States

Hackensack University Medical Center - John Theurer Cancer Center, Hackensack, New Jersey, United States

The Christ Hospital Hematology Oncology, Lindner Research Center, Cincinnati, Ohio, United States

University of Pennsylvania Hospital, Philadelphia, Pennsylvania, United States

Fox Chase Cancer Center, Philadelphia, Pennsylvania, United States

University of Pittsburgh Medical Center Hillman Cancer Center, Pittsburgh, Pennsylvania, United States

Greenville Health System Cancer Institute, Greenville, South Carolina, United States

West Cancer Center, Germantown, Tennessee, United States

Sarah Cannon Research Institute at Tennessee Oncology, Nashville, Tennessee, United States

University Of Texas Southwestern Medical Center At Dallas, Dallas, Texas, United States

Virginia Cancer Specialists, Arlington, Virginia, United States

Contact Details

Name: Mark Jones, MD

Affiliation: Incyte Corporation

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

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