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Terminated Phase 4 Interventional Results available

Extension to Study 200952 to Evaluate the Long-term Safety, Tolerability and Pharmacodynamics of Albiglutide Liquid Drug Product in Type 2 Diabetes Mellitus Subjects

ClinicalTrials.gov ID: NCT02750930

Public ClinicalTrials.gov record NCT02750930. 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 Nov 4, 2026, 12:44 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-label Extension to Study 200952 to Evaluate the Long-term Safety, Tolerability and Pharmacodynamics of Albiglutide Liquid Drug Product in Subjects With Type 2 Diabetes Mellitus

Brief summary

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

Albiglutide has been developed for the treatment of type 2 diabetes mellitus (T2DM) as an adjunct to diet and exercise, as monotherapy, or in combination with existing therapies and has been approved by the United States (US) Food and Drug Administration (FDA), the European Medicines Agency (EMA) and other regulatory agencies. This is a 26 week, open-label, single group, multicenter, extension study to Study 200952. This extension study will provide extended safety, tolerability and immunogenicity data for the albiglutide liquid drug product. This extension study will comprise 2 study periods: treatment (26 weeks) and post-treatment follow-up (8 weeks). A maximum of 300 subjects will be eligible to take part in this extension study.

Study identification

NCT ID
NCT02750930
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 4
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
8 participants

Conditions and interventions

Interventions

Drug · Device

Eligibility (public fields only)

Age range
Not listed
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
Oct 7, 2016 (Actual)
Primary completion
Mar 21, 2017 (Actual)
Completion
Mar 21, 2017 (Actual)
Last update posted
Jul 12, 2019

2016 – 2017

United States locations

U.S. sites
27
U.S. states
12
U.S. cities
25
Facility City State ZIP Site status
GSK Investigational Site Phoenix Arizona 85018 —
GSK Investigational Site Fresno California 93720 —
GSK Investigational Site Lomita California 90717 —
GSK Investigational Site Sacramento California 95831 —
GSK Investigational Site Spring Valley California 91978 —
GSK Investigational Site Tustin California 92780 —
GSK Investigational Site West Hills California 91307 —
GSK Investigational Site Littleton Colorado 80128 —
GSK Investigational Site Bradenton Florida 34201 —
GSK Investigational Site Clearwater Florida 33765 —
GSK Investigational Site Hallandale Florida 33009 —
GSK Investigational Site Miami Florida 33156 —
GSK Investigational Site Miami Florida 33176 —
GSK Investigational Site Orlando Florida 32825 —
GSK Investigational Site Conyers Georgia 30094 —
GSK Investigational Site Evansville Indiana 47714 —
GSK Investigational Site Kalamazoo Michigan 49009 —
GSK Investigational Site Chesterfield Missouri 63017 —
GSK Investigational Site Columbia North Carolina 28150 —
GSK Investigational Site Columbus Ohio 43201 —
GSK Investigational Site Columbia South Carolina 29204 —
GSK Investigational Site Arlington Texas 76012 —
GSK Investigational Site Dallas Texas 75230 —
GSK Investigational Site Houston Texas 77036 —
GSK Investigational Site Houston Texas 77058 —
GSK Investigational Site Schertz Texas 782154 —
GSK Investigational Site Shavano Prk Texas 78231 —

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 NCT02750930, 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 Jul 12, 2019 · Synced Nov 4, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02750930 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →