66
Participants
Start Date
December 8, 2017
Primary Completion Date
April 29, 2019
Study Completion Date
April 29, 2019
GDC-0334
Part 1: GDC-0334 given orally with dose escalation between cohorts, based on emerging safety and pharmacokinetic (PK) data. Parts 2 and 3: doses to be based on the safety, tolerability, and PK data generated in the study. The dosing duration in Part 3 is planned to be at least 14 days, but no longer than 28 days.
Placebo
Participants will receive GDC-0334-matching placebo.
Quotient Clinical Ltd, Clinical Research Unit, Nottingham
Lead Sponsor
Genentech, Inc.
INDUSTRY