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Brief Title: QUILT-3.055: A Study of Combination Immunotherapies in Patients Who Have Previously Received Treatment With Immune Checkpoint Inhibitors
Official Title: QUILT-3.055: A Phase IIb, Multicohort, Open-Label Study of Combination Immunotherapies in Patients Who Have Previously Received Treatment With PD-1/PD-L1 Immune Checkpoint Inhibitors
Study ID: NCT03228667
Brief Summary: This is a Phase IIb, multicohort, open-label multicenter study of combination immunotherapies in patients who have previously received treatment with PD-1/PD-L1 immune checkpoint inhibitors. All patients in Cohorts 1-4 will receive the combination treatment of PD-1/PD-L1 checkpoint inhibitor plus N-803 for up to 17 cycles. Each cycle is six weeks in duration. Some patients who experience disease progression while on study in Cohorts 1-4 may roll over into Cohort 5 and receive combination therapy with a PD-1/PD-L1 checkpoint inhibitor, N-803, and PD-L1 t-haNK cellular therapy for up to an additional 17 cycles. Each cycle is six weeks in duration. All patients will receive N-803 once every 3 weeks. Patients will also receive the same checkpoint inhibitor that they received during their previous therapy. Radiologic evaluation will occur at the end of each treatment cycle. Treatment will continue for up to 2 years, or until the patient experiences confirmed progressive disease or unacceptable toxicity, withdraws consent, or if the Investigator feels it is no longer in the patient's best interest to continue treatment. Patients will be followed for disease progression, post-therapies, and survival through 24 months past administration of the first dose of study drug.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Alaska Clinical Research Center, Anchorage, Alaska, United States
Genesis Cancer Center, Hot Springs, Arkansas, United States
Chan Soon-Shiong Institute for Medicine, El Segundo, California, United States
MemorialCare Health System, Fountain Valley, California, United States
Glendale Adventist Medical Center, Glendale, California, United States
University of Southern California Norris Comprehensive Cancer Center, Los Angeles, California, United States
Desert Hematology Oncology Medical Group, Inc., Rancho Mirage, California, United States
Memorial Healthcare System, Hollywood, Florida, United States
Miami Cancer Institute (Baptist Health South Florida), Miami, Florida, United States
University of Miami, Miami, Florida, United States
Horizon Oncology Associates, Lafayette, Indiana, United States
University of Iowa Holden Comprehensive Cancer Center, Iowa City, Iowa, United States
Baptist Health - Lexington, Lexington, Kentucky, United States
Baptist Health- Louisville, Louisville, Kentucky, United States
Dana Farber Cancer Institute, Boston, Massachusetts, United States
Henry Ford Hospital, Detroit, Michigan, United States
University of Minnesota - Masonic Cancer Center, Minneapolis, Minnesota, United States
Mercy Research Joplin, Joplin, Missouri, United States
Washington University School of Medicine, Saint Louis, Missouri, United States
Mercy Clinic Cancer & Hematology - Chub O'Reilly Cancer Center, Springfield, Missouri, United States
St. Vincent Frontier Cancer Center (SCL), Billings, Montana, United States
Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, United States
Roswell Park Cancer Institute, Buffalo, New York, United States
University of Rochester, Rochester, New York, United States
Cleveland Clinic - Main Site, Cleveland, Ohio, United States
Mercy Clinic Oklahoma City, Oklahoma City, Oklahoma, United States
Providence Portland Medical Center, Portland, Oregon, United States
Gettysburg/Hanover Cancer Centers, Gettysburg, Pennsylvania, United States
Medical University of South Carolina, Charleston, South Carolina, United States
St. Francis Cancer Center/Bon Secours St. Francis Health System, Greenville, South Carolina, United States
Spartanburg Medical Center, Spartanburg, South Carolina, United States
Sanford Clinical Research, Sioux Falls, South Dakota, United States
University of Tennessee Medical Center, Knoxville, Tennessee, United States
Oncology Consultants of Houston, Houston, Texas, United States
Bon Secours Richmond, Richmond, Virginia, United States