A Study to Evaluate the Bioavailability of Teduglutide Administered Subcutaneously by Syringe Injection Versus Pen Injector in Healthy Adult Participants

PHASE1CompletedINTERVENTIONAL
Enrollment

64

Participants

Timeline

Start Date

January 13, 2021

Primary Completion Date

August 20, 2021

Study Completion Date

August 20, 2021

Conditions
Healthy Volunteers
Interventions
DRUG

Teduglutide

Participants received 3 mg or 4 mg of Teduglutide SC syringe injection followed by pen injector or vice versa depending upon the treatment sequence AB or BA on Day 1 of Treatment Periods 1 and 2.

DEVICE

Syringe Injection

Teduglutide was administered using syringe.

DEVICE

Pen injector

Teduglutide was administered using pen injector.

Trial Locations (1)

85283

Celerion, Phoenix

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Takeda Development Center Americas, Inc.

INDUSTRY

lead

Shire

INDUSTRY

NCT04465396 - A Study to Evaluate the Bioavailability of Teduglutide Administered Subcutaneously by Syringe Injection Versus Pen Injector in Healthy Adult Participants | Biotech Hunter | Biotech Hunter