Melanoma Clinical Trial
Official title:
A Single-armed, Open-labeled and Single-centered Phase II Trial of Everolimus in Selected Patients With Metastatic Melanoma: Efficacy and Safety Study
This is a single-armed, open-labeled and single-centered study of everolimus in selective
patients with metastatic melanoma for evaluation of the efficacy and safety. The study
objective is to evaluate efficacy profile of everolimus.
The patients who comply with the inclusion and exclusion criteria will be enrolled. The
estimated recruiting duration is 18 months. Everolimus will be given in the dose of 10 mg
orally each day at lease 6 months unless disease progression or intolerance. The follow-up
is till death(at least 1 year).
n/a
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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