LivingGLP1
Study S001019

Safety, Tolerability, Pharmacokinetics, and Efficacy of LY3053102 With 12 Weeks of Treatment in Patients With Type 2 Diabetes Mellitus

Registration

Registration
NCT02020616
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1; PHASE2
Masking
TRIPLE
Status
TERMINATED
Enrollment
60
Start
2013-12
Primary completion
2015-02
Lead sponsor
Eli Lilly and Company
Conditions
Type 2 Diabetes Mellitus
Interventions
DRUG:LY3053102; DRUG:Exenatide ER; DRUG:Placebo; DRUG:Metformin
Results posted
TRUE
Individual participant data sharing
YES
Secondary identifiers
OTHER:I6I-MC-LMRB

Registered primary outcomes

  • Change From Baseline in Hemoglobin A1c (HbA1c) at 12-Week Endpoint [Baseline, Week 12]

Linked records (0)

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