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Completed Phase 2 Interventional Results available

Pharmacokinetics/Pharmacodynamics of Albiglutide

ClinicalTrials.gov ID: NCT01357889

Public ClinicalTrials.gov record NCT01357889. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 24, 2026, 9:42 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multidose Study in Subjects With Type 2 Diabetes Mellitus to Assess the Pharmacokinetics and Pharmacodynamics of Albiglutide

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The first part of the study includes a single dose treatment period to evaluate the pharmacokinetic bioequivalence of a subcutaneous injection of albiglutide from process 2 drug substance compared with process 3 drug substance. The second part of the treatment period will evaluate additional pharmacokinetic and pharmacodynamic parameters and safety and tolerability of repeat doses of albiglutide given weekly for 12 weeks from process 2 drug substance compared with process 3 drug substance. Subjects with type 2 diabetes whose glycemia is inadequately controlled on their current regimen of diet and exercise or stable dose of metformin will be recruited into the study.

Study identification

NCT ID
NCT01357889
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
283 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
18 Years to 80 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 2011 (Type not available)
Primary completion
Oct 2012 (Actual)
Completion
Oct 2012 (Actual)
Last update posted
Jan 9, 2017

2011 – 2012

United States locations

U.S. sites
30
U.S. states
15
U.S. cities
28
Facility City State ZIP Site status
GSK Investigational Site Dothan Alabama 36301 —
GSK Investigational Site Long Beach California 90806 —
GSK Investigational Site Riverside California 92506 —
GSK Investigational Site Hallandale Florida 33009 —
GSK Investigational Site Jacksonville Florida 32205 —
GSK Investigational Site Orlando Florida 32822 —
GSK Investigational Site Tampa Florida 33603 —
GSK Investigational Site Blue Ridge Georgia 30513 —
GSK Investigational Site Lexington Kentucky 40504 —
GSK Investigational Site Paducah Kentucky 42003 —
GSK Investigational Site Gulfport Mississippi 39501 —
GSK Investigational Site Picayune Mississippi 39466 —
GSK Investigational Site Omaha Nebraska 68131 —
GSK Investigational Site Greensboro North Carolina 27405 —
GSK Investigational Site Columbus Ohio 43213 —
GSK Investigational Site Mason Ohio 45040 —
GSK Investigational Site Bensalem Pennsylvania 19020 —
GSK Investigational Site Columbia South Carolina 29201 —
GSK Investigational Site North Myrtle Beach South Carolina 29582 —
GSK Investigational Site Simpsonville South Carolina 29681 —
GSK Investigational Site Clarksville Tennessee 37043 —
GSK Investigational Site McKenzie Tennessee 38201 —
GSK Investigational Site Houston Texas 77074 —
GSK Investigational Site Irving Texas 75039 —
GSK Investigational Site San Antonio Texas 78215 —
GSK Investigational Site San Antonio Texas 78218 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site Sugarland Texas 77479 —
GSK Investigational Site Bountiful Utah 84010 —
GSK Investigational Site Lewisburg West Virginia 24901 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01357889, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 9, 2017 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01357889 live on ClinicalTrials.gov.

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