LivingGLP1
Study S000351

A Dose Block-randomized, Double-blind, Placebo-controlled, Dose-escalating, Phase I Study to Evaluate Safety and Pharmacokinetics/Pharmacodynamics of DA-3091 After Subcutaneous Injection in Healthy Male Subjects

Registration

Registration
NCT01156779
Acronym
SR-Exenatide
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
31
Start
2010-07
Primary completion
2012-04
Lead sponsor
Dong-A Pharmaceutical Co., Ltd.
Conditions
Diabetes Mellitus
Interventions
DRUG:SR-exenatide
Results posted
FALSE

Registered primary outcomes

  • Assessment of safety [84 days]

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