drugset / Trial / NCT01226277

A Study Evaluating the Safety, Tolerability and Pharmacokinetics of GDC-0917 Administered to Patients With Refractory Solid Tumors or Lymphoma

NCT01226277 ↗

Phase 1 Completed 42 enrolled Genentech, Inc.
RandomizedSingle-groupOpen-labelTreatment

Summary

This is an open-label, multicenter, Phase I dose-escalation study designed to assess the safety, tolerability, and pharmacokinetics (PK) of GDC-0917 in patients with refractory solid tumors or lymphoma.

Timeline

Start
2010-10
Primary completion
2012-09
Completion
2012-09

Drugs

EvaluationDrugModalityDoseRoute
Subject GDC-0917 Small molecule — Oral

Indications

No indication recorded.