CompletedPhase 2NCT01642186
Study of (1) Everolimus, (2) Estrogen Deprivation Therapy (EDT) With Leuprolide + Letrozole and (3) Everolimus + EDT in Patients With Unresectable Fibrolamellar Hepatocellular Carcinoma (FLL-HCC)
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
- Memorial Sloan Kettering Cancer Center
- Principal Investigator
- Ghassan Abou-Alfa, MDMemorial Sloan Kettering Cancer Center
- Intervention
- everolimus(drug)
- Enrollment
- 28 target
- Eligibility
- 12 years · All sexes
- Timeline
- 2012 – 2021
Study locations (6)
- University of California San Francisco, San Francisco, California, United States
- John Hopkins Medical Center, Baltimore, Maryland, United States
- Massachusetts General Hospital Cancer Center, Boston, Massachusetts, United States
- Brigham and Women's Hospital, Boston, Massachusetts, United States
- Dana-Farber Cancer Institute, Boston, Massachusetts, United States
- Memorial Sloan Kettering Cancer Center, New York, New York, United States
Collaborators
Fibrolamellar Cancer Foundation · Dana-Farber Cancer Institute · Johns Hopkins University · University of California, San Francisco · Abbott · Novartis Pharmaceuticals
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 NCT01642186 on ClinicalTrials.govOther trials for Fibrolamellar hepatocellular carcinoma
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