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
Registered primary outcomes
- Percentage of Participants With Adverse Events(AEs) and Serious Adverse Event(SAEs) [baseline and 12/24 weeks]
Linked records (0)
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