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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 Jul 23, 2026, 6:20 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. 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

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

  • Albiglutide Drug
  • Auto-injector Device

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 6, 2016
Primary completion
Mar 20, 2017
Completion
Mar 20, 2017
Last update posted
Jul 11, 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 11, 2019 · Synced Jul 23, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02750930 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →