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Brief Title: INCMGA00012 in Combination With Other Therapies in Patients With Advanced Solid Tumors
Official Title: A Phase 1b Study of INCMGA00012 in Combination With Other Therapies in Patients With Advanced Solid Tumors
Study ID: NCT03589651
Brief Summary: The purpose of this study is to determine the safety, preliminary evidence of clinical activity, and recommended Phase 2 dose (RP2D) of INCMGA00012 in combination with other agents that may improve the therapeutic efficacy of anti-PD-1 monotherapy.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
The Angeles Clinic and Research Institute, Los Angeles, California, United States
Yale New Haven Hospital, New Haven, Connecticut, United States
University of Florida - Shands Cancer Center, Gainesville, Florida, United States
University of Chicago Medical Center, Chicago, Illinois, United States
Rutgers Cancer Institute of Nj, New Brunswick, New Jersey, United States
Roswell Park Cancer Institute, Buffalo, New York, United States
Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, United States
Upmc Cancercenter, Pittsburgh, Pennsylvania, United States
South Texas Accelerated Research Therapeutics, San Antonio, Texas, United States