LivingGLP1
Study S001619

A Dose Block-randomized, Double-blind, Placebo-controlled, Dose-escalating Study to Evaluate Safety and Pharmacokinetics/Pharmacodynamics of SR Exenatide (PT302) After Subcutaneous Injection in Healthy Male Volunteers

Registration

Registration
NCT00964262
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
TRIPLE
Status
COMPLETED
Enrollment
34
Start
2009-08
Primary completion
2010-10
Lead sponsor
Peptron, Inc.
Conditions
Type 2 Diabetes Mellitus
Interventions
DRUG:SR Exenatide (PT302); DRUG:Placebo
Results posted
FALSE

Registered primary outcomes

  • To evaluate the safety and pharmacokinetics of SR exenatide (PT302) in healthy subjects after a single subcutaneous injection [8 weeks]

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
R0023956Pharmacokinetic properties and effects of PT302 after repeated oral glucose loading tests in a dose-escalating study.
Gu N, Clinical therapeutics
2014Randomized trialPMID 24373998DOIcites ClinicalTrials.gov:NCT00964262; registry reference DERIVED:24373998