A Study to Compare Pharmacokinetics (PK) of Etrolizumab Administered Subcutaneously by a Prefilled Syringe With Needle Safety Device (PFS-NSD) or an Auto-injector (AI)

PHASE1CompletedINTERVENTIONAL
Enrollment

180

Participants

Timeline

Start Date

December 7, 2016

Primary Completion Date

April 9, 2018

Study Completion Date

April 9, 2018

Conditions
Healthy Volunteers
Interventions
DRUG

Etrolizumab

Etrolizumab will be administered at a dose of 105 milligrams (mg).

DEVICE

Auto-Injector (AI)

The pre-filled AI will be used to administer etrolizumab.

DEVICE

Prefilled Syringe With Needle Safety Device (PFS-NSD)

The PFS-NSD will be used to administer etrolizumab.

Trial Locations (4)

32117

Covance Research Unit - Daytona, Daytona Beach

47710

Covance Clinical Research Unit Inc.; Covance Gfi Research, Evansville

53704

Covance Clinical Research Unit, Inc, Madison

75247

Covance Research Unit - Dallas, Dallas

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Genentech, Inc.

INDUSTRY