drugset / Trial / NCT01356173

Evaluating the Safety and Tolerability of GDC-0349 in Patients With Locally Advanced or Metastatic Solid Tumors or Non Hodgkin's Lymphoma

NCT01356173 ↗

Phase 1 Completed 10 enrolled Genentech, Inc.
RandomizedSingle-groupOpen-labelTreatment

Summary

This is an open-label, multicenter, Phase I, dose-escalation study to assess the safety, tolerability, and pharmacokinetic (PK) of GDC-0349 administered once daily (QD), orally (PO).

Timeline

Start
2011-06
Primary completion
2012-12
Completion
2012-12

Drugs

EvaluationDrugModalityDoseRoute
Subject RG-7603 Small molecule — Oral

Indications