LivingGLP1
Study S000748

A Repeat-dose Study in Subjects With Type 2 Diabetes Mellitus to Assess the Efficacy, Safety, Tolerability and Pharmacodynamics, of Albiglutide Liquid Drug Product

Registration

Registration
NCT02683746
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
DOUBLE
Status
COMPLETED
Enrollment
308
Start
2016-03-16
Primary completion
2017-04-03
Lead sponsor
GlaxoSmithKline
Conditions
Diabetes Mellitus, Type 2
Interventions
DRUG:Lyophilized albiglutide DCC pen injector; DRUG:Lyophilized albiglutide DCC pen injector matching placebo; DRUG:Albiglutide liquid auto-injector; DRUG:Albiglutide liquid auto-injector matching placebo
Results posted
TRUE
Individual participant data sharing
YES

Registered primary outcomes

  • Change From Baseline in Glycated Hemoglobin (HbA1c) at Week 26 [Baseline and Week 26]

Linked records (1)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R0022858Efficacy and safety of an albiglutide liquid formulation compared with the lyophilized formulation: A 26-week randomized, double-blind, repeat-dose study in patients with type 2 diabetes mellitus.
Shaddinger BC, Diabetes research and clinical practice
2019Randomized trialPMID 31004676DOIregistry reference BACKGROUND:31004676