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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Key facts

Sponsor
Memorial Sloan Kettering Cancer Center
Principal Investigator
Ghassan Abou-Alfa, MD
Memorial Sloan Kettering Cancer Center
Intervention
everolimus(drug)
Enrollment
28 target
Eligibility
12 years · All sexes
Timeline
20122021

Study locations (6)

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.gov

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