drugset / Trial / NCT00106431

A Single Agent Phase II Study of Romidepsin (Depsipeptide, FK228) in the Treatment of Cutaneous T-cell Lymphoma (CTCL)

NCT00106431

Phase 2 Completed 102 enrolled Celgene Corporation
Non-randomizedSingle-groupOpen-labelTreatment

Summary

GPI-04-0001 was a Phase II, non-randomized, open label, single arm study that was conducted at approximately 30 sites, primarily in the United States, Europe and Russia. It assessed the efficacy, safety, and tolerability of romidepsin as a treatment for cutaneous T-cell lymphoma (CTCL). Study patients (pts) received romidepsin in a dose of 14 mg/m\^2 intravenously over 4 hours on Days 1, 8 and 15 of each 28-day cycle. The duration of study treatment was 6 cycles although pts who showed an objective response or stable disease could continue to receive therapy, at the discretion of the investigator, until disease progression or another withdrawal criterion was met.

Timeline

Start
2005-01-01
Primary completion
2008-06-01
Completion
2008-12-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Romidepsin Peptide 14 mg/m2 Intravenous