RecruitingPhase 1NCT04617522
Study of Sacituzumab Govitecan in Participants With Advanced or Metastatic Solid Tumor and Moderate Liver Impairment
Studying Fibrolamellar hepatocellular carcinoma
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Gilead Sciences
- Principal Investigator
- Gilead Study DirectorGilead Sciences
- Intervention
- Sacituzumab Govitecan-hziy(drug)
- Enrollment
- 30 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2021 – 2026
Study locations (13)
- Pacific Shores Medical Group, Long Beach, California, United States
- Christiana Care Health Services, Newark, Delaware, United States
- University of Maryland, Baltimore, Maryland, United States
- NEXT Austin, 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
- Texas Liver Institute, San Antonio, Texas, United States
- NEXT Oncology, San Antonio, Texas, United States
- Institut Bergonie Medical Oncology, Bordeaux, France
- Centre Leon Berard, Lyon, France
- Institut de Cancerologie de l'Ouest (ICO) - Saint-Herblain, Saint-Herblain, France
- Institut Català d'Oncologia - L'Hospitalet de Llobregat, Barcelona, Spain
- Hospital Universitario Virgen del Rocío, Seville, Spain
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.
Open NCT04617522 on ClinicalTrials.govOther trials for Fibrolamellar hepatocellular carcinoma
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