LivingGLP1
Study S000173

A 12/24-weeks, Open, Multi-centre, Phase IV Study on Safety and Efficacy of 2mg Exenatide Once Weekly (Bydureon) in Patients With Type 2 Diabetes Mellitus

Registration

Registration
NCT02533453
Acronym
Bydureon
Study type
INTERVENTIONAL
Phase
PHASE4
Masking
NONE
Status
COMPLETED
Enrollment
110
Start
2016-01-28
Primary completion
2016-12-07
Lead sponsor
AstraZeneca
Conditions
Type 2 Diabetes Mellitus
Interventions
BIOLOGICAL:Bydureon
Results posted
TRUE

Registered primary outcomes

  • Percentage of Participants With Adverse Events(AEs) and Serious Adverse Event(SAEs) [baseline and 12/24 weeks]

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