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Clinical Trial Summary

This open-label, Phase I study will evaluate the safety, tolerability, and pharmacokinetics of increasing doses of GDC-0853 in patients with relapsed or refractory B-cell non-Hodgkin's lymphoma or chronic lymphocytic leukemia. In a dose-expansion part, GDC-0853 will be assessed in subsets of patients.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01991184
Study type Interventional
Source Genentech, Inc.
Contact
Status Completed
Phase Phase 1
Start date December 16, 2013
Completion date March 8, 2022