LivingGLP1
Study S002169

An Exploratory Study of the Effect of Treatment Interruption on Safety of Exenatide in Patients With Type 2 Diabetes

Registration

Registration
NCT00516048
Study type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Phase
PHASE3
Masking
NONE
Status
COMPLETED
Enrollment
58
Start
2007-08
Primary completion
2008-04
Lead sponsor
AstraZeneca
Conditions
Type 2 Diabetes Mellitus
Interventions
DRUG:exenatide
Results posted
TRUE

Registered primary outcomes

  • Treatment-emergent Antibody Status (Maximum Titer Level Experienced) [24 weeks]
  • Incidence of Potentially Immune-related Treatment-emergent Adverse Events [24 weeks]

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