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Spots Global Cancer Trial Database for Rollover Study in Participants With Metastatic Solid Tumors Benefiting From Therapy With Sacituzumab Govitecan-hziy

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Trial Identification

Brief Title: Rollover Study in Participants With Metastatic Solid Tumors Benefiting From Therapy With Sacituzumab Govitecan-hziy

Official Title: Open-label Rollover Study to Evaluate Long-Term Safety in Subjects With Metastatic Solid Tumors That Are Benefiting From Continuation of Therapy With Sacituzumab Govitecan

Study ID: NCT04319198

Study Description

Brief Summary: The goal of this clinical study is to learn more about the study drug, sacituzumab govitecan-hziy, and how safe it is in participants with metastatic cancer (cancer that has spread).

Detailed Description: This is a rollover study. Only participants who continue to receive clinical benefit from continuation of sacituzumab govitecan-hziy therapy and are tolerating therapy at the time of enrollment are eligible for this study. Participants enrolled may continue to receive sacituzumab govitecan-hziy at the dose that they were receiving in the Gilead parent study at the time of consenting to participate in this rollover study.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

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

Rocky Mountain Cancer Center, Aurora, Colorado, United States

Christiana Care Health Services, Christiana Hospital, Newark, Delaware, United States

Florida Cancer Specialists & Research Institute, Fort Myers, Florida, United States

Baptist Health - Miami Cancer Institute, Miami, Florida, United States

Illinois Cancer Specialists, Arlington Heights, Illinois, United States

University of Chicago, Chicago, Illinois, United States

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

Massachusetts General Hospital, Boston, Massachusetts, United States

Dana Farber Cancer Institute, Boston, Massachusetts, United States

New York Cancer & Blood Specialists - Setauket Medical Oncology, Port Jefferson, New York, United States

UPMC Hillman Cancer Center, Pittsburgh, Pennsylvania, United States

Next Oncology, Austin, Texas, United States

Oncology Consultants,P.A., Houston, Texas, United States

The University of Texas M.D. Anderson Cancer Center, Houston, Texas, United States

NEXT Oncology, San Antonio, Texas, United States

Institut Jules Bordet, Bruxelles, , Belgium

CHU UCL NAMUR - Sainte Elisabeth, Namur, , Belgium

Institut Bergonie, Bordeaux Cedex, , France

Centre Leon Berard, Lyon, , France

Institut Claudius Regaud, Toulouse Cedex 9, , France

Contact Details

Name: Gilead Study Director

Affiliation: Gilead Sciences

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

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