TerminatedPhase 2NCT04476329
Optimization for Regorafenib in HCC
Studying Adult hepatocellular carcinoma
Last synced from ClinicalTrials.gov
ℹ
Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- SC Liver Research Consortium, LLC
- Principal Investigator
- Catherine T Frenette, MD, M.D., Ph.DScripps MD Anderson Cancer Center
- Intervention
- Regorafenib 40 MG(drug)
- Enrollment
- 7 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2021 – 2021
Study locations (9)
- Banner MD Anderson Cancer Center, Gilbert, Arizona, United States
- VA Long Beach Health System, Long Beach, California, United States
- Tulane University, New Orleans, Louisiana, United States
- Henry Ford Health Systems, Detroit, Michigan, United States
- Cancer and Hematology Centers of Western Michigan, Grand Rapids, Michigan, United States
- Saint Louis University, St Louis, Missouri, United States
- Comprehensive Cancer Centers of Nevada, Henderson, Nevada, United States
- University of Cincinnati Medical Center, Cincinnati, Ohio, United States
- Albert Einstein Medical Center, Philadelphia, Pennsylvania, United States
Collaborators
Bayer
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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