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Spots Global Cancer Trial Database for Phase 1/1b Study to Evaluate the Safety and Tolerability of Ciforadenant Alone and in Combination With Atezolizumab in Advanced Cancers

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Trial Identification

Brief Title: Phase 1/1b Study to Evaluate the Safety and Tolerability of Ciforadenant Alone and in Combination With Atezolizumab in Advanced Cancers

Official Title: A Phase 1/1b, Open-Label, Multicenter, Repeat-Dose, Dose-Selection Study of Ciforadenant as Single Agent and in Combination With Atezolizumab in Patients With Selected Incurable Cancers

Study ID: NCT02655822

Study Description

Brief Summary: This is a phase 1/1b open-label, multicenter, dose-selection study of ciforadenant, an oral small molecule targeting the adenosine-A2A receptor on T-lymphocytes and other cells of the immune system. This trial will study the safety, tolerability, and anti-tumor activity of ciforadenant as a single agent and in combination with atezolizumab, a PD-L1 inhibitor against various solid tumors. Ciforadenant blocks adenosine from binding to the A2A receptor. Adenosine suppresses the anti-tumor activity of T cells and other immune cells.

Detailed Description: This is a phase 1/1b open-label, multicenter, dose-selection study of ciforadenant, an oral small molecule targeting the adenosine-A2A receptor on T-lymphocytes and other cells of the immune system. This trial will study the safety, tolerability, and anti-tumor activity of ciforadenant as a single agent and in combination with atezolizumab, an intravenous PD-L1 inhibitor. Ciforadenant blocks adenosine from binding to the A2A receptor. Adenosine suppresses the anti-tumor activity of T cells and other immune cells.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

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

University of California - San Francisco, San Francisco, California, United States

Stanford Cancer Institute, Stanford, California, United States

Yale University, New Haven, Connecticut, United States

University of Miami Hospital and Clinics, Miami, Florida, United States

Rush University Medical Center, Chicago, Illinois, United States

University of Chicago Medical Center, Chicago, Illinois, United States

Sidney Kimmel Comprehensive Cancer Center - Johns Hopkins University School of Medicine, Baltimore, Maryland, United States

Massachusetts General Hospital, Boston, Massachusetts, United States

Karmanos Cancer Institute, Detroit, Michigan, United States

Roswell Park Cancer Institute, Buffalo, New York, United States

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

Cleveland Clinic, Cleveland, Ohio, United States

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

Medical College of Wisconsin, Milwaukee, Wisconsin, United States

Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia

Monash Health, Clayton, Victoria, Australia

Cross Cancer Institute, Edmonton, Alberta, Canada

British Columbia Cancer Agency - Vancouver Centre, Vancouver, British Columbia, Canada

The Ottawa Hospital Cancer Centre, Ottawa, Ontario, Canada

Contact Details

Name: Mehrdad Mobasher, MD, MPH

Affiliation: Corvus Pharmaceuticals

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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