LivingGLP1
Study S000494

A Multidose Study in Subjects With Type 2 Diabetes Mellitus to Assess the Pharmacokinetics and Pharmacodynamics of Albiglutide

Registration

Registration
NCT01357889
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
DOUBLE
Status
COMPLETED
Enrollment
283
Start
2011-07
Primary completion
2012-10
Lead sponsor
GlaxoSmithKline
Conditions
Diabetes Mellitus, Type 2
Interventions
BIOLOGICAL:albiglutide (GSK716155)
Results posted
TRUE
Individual participant data sharing
YES

Registered primary outcomes

  • Area Under the Plasma Concentration Versus Time Curve (AUC) From Time Zero to Infinity (0-inf) of Albiglutide in the Bioequivalence (BE) Phase [Pre-dose at Baseline; 24 hours (hr), 48 hr, 96 hr, 216 hr, 312 hr, 480 hr, and 672 hr post-dose]
  • Maximum Observed Plasma Concentration (Cmax) of Albiglutide in the BE Phase [Pre-dose at Baseline; 24 hr, 48 hr, 96 hr, 216 hr, 312 hr, 480 hr, and 672 hr post-dose]

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
R0018591Clinical pharmacology of albiglutide, a GLP-1 receptor agonist.
Young MA, Postgraduate medicine
2014Other trialPMID 25387217DOIcites ClinicalTrials.gov:NCT01357889; registry reference DERIVED:25387217