LivingGLP1
Study S001731

A Safety, Tolerability, Pharmacokinetic, and Pharmacodynamic Study of LY3325656 After Single Dose in Healthy Subjects and Patients With Type 2 Diabetes

Registration

Registration
NCT03115099
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
80
Start
2017-05-31
Primary completion
2018-04-05
Lead sponsor
Eli Lilly and Company
Conditions
Diabetes Mellitus, Type 2
Interventions
DRUG:LY3325656; DRUG:Placebo; DRUG:Liraglutide; DRUG:Sitagliptin
Results posted
FALSE
Secondary identifiers
OTHER:I8U-MC-DMBA

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 [Baseline through approximately 12 weeks and 5 weeks after first administration of study drug in Parts A and B, respectively]

Linked records (1)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R004963420-OR: GPR142 Agonists Increase Glucose-Dependent Insulin Secretion and Differentially Regulate Hormone Secretion in Preclinical and Phase 1 Studies
Edward John Pratt, Diabetes
2019Other trialDOIcites ClinicalTrials.gov:NCT03115099