LivingGLP1
Study S001658

An Adaptive Design Study for the Assessment of the Pharmacokinetics of Albiglutide in Subjects With Normal Renal Function and Subjects With Moderate-to-severe Renal Impairment and Hemodialysis.

Registration

Registration
NCT00938158
Study type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
75
Start
2009-08-05
Primary completion
2011-04-12
Lead sponsor
GlaxoSmithKline
Conditions
Diabetes Mellitus, Type 2
Interventions
BIOLOGICAL:albiglutide
Results posted
FALSE
Individual participant data sharing
YES

Registered primary outcomes

  • The primary objective is to characterize the PK of albiglutide in subjects with type 2 diabetes and varying degrees of renal impairment, including subjects requiring hemodialysis, and in age, gender and BMI-matched subjects. [42 days]

Linked records (2)

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:NCT00938158; registry reference DERIVED:25387217
R0025635Effect of renal impairment on the pharmacokinetics, efficacy, and safety of albiglutide.
Young MA, Postgraduate medicine
2014Randomized trialPMID 24918790DOIcites ClinicalTrials.gov:NCT00938158; registry reference DERIVED:24918790