drugset / Trial / NCT00046735

Phase 1 Study OF CDC-501 in Patients With Solid Tumors

NCT00046735 ↗

Phase 1 Completed 24 enrolled Celgene Corporation
NaSingle-groupOpen-labelTreatment

Summary

To identify the maximum tolerated dose (MTD) and safety of CDC-501 when given in a 6-week cycle in patients with solid tumors that are refractory after standard treatment.

Timeline

Start
2002-06-01
Primary completion
2006-08-01
Completion
2006-09-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Lenalidomide Other / unclassified 5 mg —
Subject Lenalidomide Other / unclassified 10 mg —
Subject Lenalidomide Other / unclassified 25 mg —

Indications