drugset / Trial / NCT01168752

Study of Debio 0932 in Patients With Advanced Solid Tumours or Lymphoma

NCT01168752

Phase 1 Completed 81 enrolled Debiopharm International SA
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the maximum tolerated dose of Debio 0932 when administered orally, every-other-day or daily during the first 30 days, in patients with solid tumours or lymphoma.

Timeline

Start
2010-04
Primary completion
2013-04
Completion
2013-04

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject CUDC-305 Small molecule 50 mg Oral
Subject CUDC-305 Small molecule 1000 mg Oral
Subject CUDC-305 Small molecule 1600 mg Oral

Indications