drugset / Trial / NCT01908413

Phase I Study to Assess the Safety, Tolerability and Pharmacokinetics of CUDC-427 When Given to Patients With Advanced and Refractory Solid Tumors or Lymphoma

NCT01908413 ↗

Phase 1 Terminated 23 enrolled Curis, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This is a phase I, open-label, dose-escalation study of CUDC-427 in patients with advanced or refractory solid tumors or lymphoma. CUDC-427 is a drug that is designed to antagonize proteins that prevent or interfere with cell death. The study is designed to assess the safety, including the maximum tolerated dose, the pharmacokinetics, and the anti-cancer activity of CUDC-427.

Timeline

Start
2013-07
Primary completion
2015-03
Completion
2015-11

Drugs

EvaluationDrugModalityDoseRoute
Subject GDC-0917 Small molecule — Oral

Indications