LivingGLP1
Study S001557

A 52-Week, Open-Label, Multicenter Study to Determine the Long Term Safety and Efficacy of Albiglutide in Combination With Monotherapy of Oral Antihyperglycemic Medications in Japanese Patients With Type 2 Diabetes Mellitus

Registration

Registration
NCT01777282
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
NONE
Status
COMPLETED
Enrollment
374
Start
2013-02-23
Primary completion
2015-01-27
Lead sponsor
GlaxoSmithKline
Conditions
Diabetes Mellitus
Interventions
DRUG:Albiglutide; DRUG:Sulfonylurea; DRUG:Biguanide; DRUG:Glinide; DRUG:Thiazolidinedione; DRUG:Alpha-glucosidase inhibitor
Results posted
TRUE
Individual participant data sharing
YES

Registered primary outcomes

  • Number of Participants With Any Adverse Event (AE) or Any Serious Adverse Event (SAE) [From Baseline through Week 52]
  • Number of Participants With Any Hypoglycemic Event [From Baseline through Week 52]

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
R0021319Albiglutide, a weekly GLP-1 receptor agonist, improves glycemic parameters in Japanese patients with type 2 diabetes over 1 year when added to single oral antidiabetic drugs.
Okuda I, Current medical research and opinion
2017Randomized trialPMID 27852119DOIcites ClinicalTrials.gov:NCT01777282; registry reference DERIVED:27852119