LivingGLP1
Study S001246

Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Multiple Doses of LY3025876 in Patients With Type 2 Diabetes Mellitus

Registration

Registration
NCT01870297
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
72
Start
2013-06
Primary completion
2014-12
Lead sponsor
Eli Lilly and Company
Conditions
Type 2 Diabetes Mellitus
Interventions
DRUG:LY3025876; DRUG:Placebo; DRUG:Liraglutide
Results posted
TRUE
Secondary identifiers
OTHER:I6D-MC-SMRB

Registered primary outcomes

  • Number of Participants With One or More Serious Adverse Event(s) (SAEs) Considered by the Investigator to be Related to Study Drug Administration [Predose on Day 1 up to Day 56 in each Part]

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