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Completed Phase 3 Interventional Results available

Safety and Efficacy of Albiglutide + Insulin Glargine Versus Insulin Lispro + Insulin Glargine Subjects With Type 2 Diabetes Mellitus

ClinicalTrials.gov ID: NCT02229227

Public ClinicalTrials.gov record NCT02229227. 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 22, 2026, 8:21 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

Study 200977: Albiglutide + Insulin Glargine Versus Insulin Lispro + Insulin Glargine in the Treatment of Subjects With Type 2 Diabetes Mellitus: The Switch Study

Study identification

NCT ID
NCT02229227
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
814 participants

Conditions and interventions

Interventions

  • Albiglutide Drug
  • Insulin Glargine and Insulin Lispro Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Nov 20, 2014
Primary completion
Jul 23, 2017
Completion
Jul 23, 2017
Last update posted
Nov 26, 2020

2014 – 2017

United States locations

U.S. sites
39
U.S. states
16
U.S. cities
37
Facility City State ZIP Site status
GSK Investigational Site Searcy Arkansas 72143
GSK Investigational Site Huntington Beach California 92648
GSK Investigational Site Long Beach California 90807
GSK Investigational Site Los Angeles California 90017
GSK Investigational Site Tustin California 92780
GSK Investigational Site West Hills California 91307
GSK Investigational Site Colorado Springs Colorado 80909
GSK Investigational Site Brooksville Florida 34601
GSK Investigational Site Clearwater Florida 33765
GSK Investigational Site Hialeah Florida 33012
GSK Investigational Site Miami Florida 33156
GSK Investigational Site Orlando Florida 32825
GSK Investigational Site Pembroke Pines Florida 33027
GSK Investigational Site Tampa Florida 33634
GSK Investigational Site West Palm Beach Florida 33401
GSK Investigational Site Chicago Illinois 60612
GSK Investigational Site Paducah Kentucky 42003
GSK Investigational Site Lake Charles Louisiana 70601
GSK Investigational Site Shreveport Louisiana 71105
GSK Investigational Site Kalamazoo Michigan 49009
GSK Investigational Site Springfield Missouri 65807
GSK Investigational Site Las Vegas Nevada 89119
GSK Investigational Site Staten Island New York 10301
GSK Investigational Site Shelby North Carolina 28150
GSK Investigational Site Wilmington North Carolina 28401
GSK Investigational Site Columbus Ohio 43213
GSK Investigational Site Dayton Ohio 45439
GSK Investigational Site Kettering Ohio 45429
GSK Investigational Site Austin Texas 78749
GSK Investigational Site Austin Texas 78756
GSK Investigational Site Dallas Texas 75230
GSK Investigational Site Houston Texas 77058
GSK Investigational Site Houston Texas 77099
GSK Investigational Site Pharr Texas 78577
GSK Investigational Site Round Rock Texas 78681
GSK Investigational Site Sugar Land Texas 77479
GSK Investigational Site Hampton Virginia 23666
GSK Investigational Site Renton Washington 98057
GSK Investigational Site Tacoma Washington 98405

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 118 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02229227, 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 Nov 26, 2020 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02229227 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →