LivingGLP1
Study S001665

A Multiple-Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of LY3437943 in Patients With Type 2 Diabetes Mellitus

Registration

Registration
NCT04143802
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
72
Start
2019-12-18
Primary completion
2020-12-28
Lead sponsor
Eli Lilly and Company
Conditions
Diabetes Mellitus, Type 2
Interventions
DRUG:LY3437943; DRUG:Dulaglutide; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
NO
Secondary identifiers
OTHER:J1I-MC-GZBB

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 Day 106]

Linked records (2)

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
R0019180The novel GIP, GLP-1 and glucagon receptor agonist retatrutide delays gastric emptying.
Urva S, Diabetes, obesity & metabolism
2023Randomized trialPMID 37311727DOIcites ClinicalTrials.gov:NCT04143802
R0014993LY3437943, a novel triple GIP, GLP-1, and glucagon receptor agonist in people with type 2 diabetes: a phase 1b, multicentre, double-blind, placebo-controlled, randomised, multiple-ascending dose trial.
Urva S, Lancet (London, England)
2022Randomized trialPMID 36354040DOIcites ClinicalTrials.gov:NCT04143802; registry reference DERIVED:36354040