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Spots Global Cancer Trial Database for CB-839 With Everolimus vs. Placebo With Everolimus in Participants With Renal Cell Carcinoma (RCC)

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Trial Identification

Brief Title: CB-839 With Everolimus vs. Placebo With Everolimus in Participants With Renal Cell Carcinoma (RCC)

Official Title: A Randomized, Double-Blind, Placebo-Controlled Phase 2 Study Comparing CB-839 in Combination With Everolimus (CBE) vs. Placebo With Everolimus (PboE) in Patients With Advanced or Metastatic Renal Cell Carcinoma (RCC)

Study ID: NCT03163667

Study Description

Brief Summary: The primary objective of this study is to compare the progression-free survival (PFS) of participants treated with telaglenastat and everolimus versus placebo and everolimus for advanced or metastatic clear cell renal cell carcinoma (ccRCC) previously treated with the following: * At least 2 lines of therapy, including at least 1 vascular endothelial growth factor tyrosine kinase inhibitor (VEGF TKI) * Radiographic progression of metastatic RCC must have occurred (per investigator assessment) on or after the most recent systemic therapy and within 6 months prior to cycle 1 day 1

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

The University of Arizona Cancer Center, Tucson, Arizona, United States

Highlands Oncology Group, Rogers, Arkansas, United States

Los Angeles Hematology Oncology Medical Group, Los Angeles, California, United States

UCLA Department of Medicine - Hematology/Oncology, Los Angeles, California, United States

Stanford Cancer Center, Stanford, California, United States

Florida Cancer Specialists- South, Fort Myers, Florida, United States

Florida Cancer Specialists- North, Saint Petersburg, Florida, United States

University Cancer & Blood Center, LLC, Athens, Georgia, United States

Northwest Georgia Oncology Centers, P.C., Marietta, Georgia, United States

St. Luke's Mountain States Tumor Institute, Boise, Idaho, United States

Northwestern University, Chicago, Illinois, United States

Parkview Research Center, Fort Wayne, Indiana, United States

University of Iowa Hospitals and Clinics, Iowa City, Iowa, United States

Norton Cancer Institute, Norton Healthcare Pavilion, Louisville, Kentucky, United States

Ochsner Clinical Foundation, New Orleans, Louisiana, United States

Anne Arundel Medical Center Oncology and Hematology, Annapolis, Maryland, United States

University of Maryland, Greenebaum Comprehensive Cancer Center, Baltimore, Maryland, United States

Metro-Minnesota Community Oncology Research Consortium, Saint Louis Park, Minnesota, United States

Mercy Clinic Oncology & Hematology, Joplin, Missouri, United States

SCRI HCA Midwest, Kansas City, Missouri, United States

Washington University School of Medicine, Saint Louis, Missouri, United States

St. Vincent Frontier Cancer Center, Billings, Montana, United States

Comprehensive Cancer Centers of Nevada, Las Vegas, Nevada, United States

Montefiore Medical Center, Bronx, New York, United States

North Shore Hematology Oncology Associates PC DBA NY Cancer and Blood Specialists, East Setauket, New York, United States

NYU Winthrop Hospital - Cancer Clinical Trials Oncology/Hematology, Mineola, New York, United States

Memorial Sloan Kettering Cancer Center, New York, New York, United States

SUNY Upstate Medical University, Syracuse, New York, United States

University of Cincinnati Medical Center, Cincinnati, Ohio, United States

Ann B. Barshinger Cancer Institute / Lancaster General Hospital, Lancaster, Pennsylvania, United States

Monongahela Valley Hospital, Monongahela, Pennsylvania, United States

Charleston Hematology Oncology Associates,PA, Charleston, South Carolina, United States

UT/Erlanger Oncology & Hematology, Chattanooga, Tennessee, United States

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

The University of Texas MD Anderson Cancer Center, Houston, Texas, United States

Utah Cancer Specialists, Salt Lake City, Utah, United States

Wenatchee Valley Hospital and Clinics, Wenatchee, Washington, United States

University of Wisconsin Carbone Cancer Center, Madison, Wisconsin, United States

Contact Details

Name: Sam Whiting

Affiliation: Calithera Biosciences

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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