drugset / Trial / NCT01169298

A Phase I, Multicenter, Open-label, Dose-escalation Study to Assess the Safety of Lenalidomide in Patients With Advanced Adult T-cell Leukemia-lymphoma and Peripheral T-cell Lymphomaperipheral T-cell Lymphoma

NCT01169298 ↗

Phase 1 Completed 13 enrolled Celgene Corporation
NaSingle-groupOpen-labelTreatment

Summary

To determine the maximum tolerated dose of lenalidomide in patients with adult T-cell leukemia-lymphoma (ATL) and peripheral T-cell lymphoma (PTCL) who have previously received therapy for ATL and PTCL

Timeline

Start
2010-07-01
Primary completion
2013-12-01
Completion
2013-12-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Lenalidomide Other / unclassified 25 mg —
Subject Lenalidomide Other / unclassified 35 mg —