LivingGLP1
Study S001004

Post Marketing Surveillance Study of Byetta ™ (Exenatide) Use Among Filipino Patients

Registration

Registration
NCT00622323
Study type
OBSERVATIONAL
Status
COMPLETED
Enrollment
41
Start
2008-02
Primary completion
2009-09
Lead sponsor
AstraZeneca
Conditions
Type 2 Diabetes Mellitus
Results posted
FALSE
Secondary identifiers
OTHER:H8O-PH-B006

Registered primary outcomes

  • To determine the proportion of patients experiencing an adverse event and a list of the experienced adverse events, that would occur among Filipino patients with type 2 diabetes and inadequate glycemic control treated with exenatide [12 weeks]

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