Open-label, Bioequivalence Study of Certolizumab Pegol 200 mg Solution Injected Either by a Prefilled Syringe (Reference) or by an E-Device (Test) in Healthy Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

100

Participants

Timeline

Start Date

March 31, 2016

Primary Completion Date

November 30, 2016

Study Completion Date

November 30, 2016

Conditions
Healthy
Interventions
DEVICE

Prefilled syringe (PFS)

Active substance: Certolizumab Pegol Pharmaceutical form: Solution for injection Administration: By prefilled syringe (PFS)

DEVICE

e-Device

Active substance: Certolizumab Pegol Pharmaceutical form: Solution for injection Administration: By e-Device

Trial Locations (1)

Unknown

Ra0132 001, Baltimore

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Parexel

INDUSTRY

lead

UCB BIOSCIENCES, Inc.

INDUSTRY