A Study of the Safety, Tolerability, Pharmacokinetics and Pharmacodynamic Effects of Single and Multiple Ascending Doses of GDC-0334 and the Effect of Food on the Pharmacokinetics of GDC-0334 in Healthy Adult Participants

PHASE1TerminatedINTERVENTIONAL
Enrollment

66

Participants

Timeline

Start Date

December 8, 2017

Primary Completion Date

April 29, 2019

Study Completion Date

April 29, 2019

Conditions
Healthy Volunteers
Interventions
DRUG

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.

DRUG

Placebo

Participants will receive GDC-0334-matching placebo.

Trial Locations (1)

NG11 6JS

Quotient Clinical Ltd, Clinical Research Unit, Nottingham

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Genentech, Inc.

INDUSTRY