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Spots Global Cancer Trial Database for QUILT-3.055: A Study of Combination Immunotherapies in Patients Who Have Previously Received Treatment With Immune Checkpoint Inhibitors

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Trial Identification

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

Study Description

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:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

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

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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