LivingGLP1
Study S002331

A Multiple Dose Human Tolerability and Pharmacokinetic Study of IBI362 in Chinese Patients With Type 2 Diabetes Mellitus and Poor Glycemic Control

Registration

Registration
NCT04466904
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1; PHASE2
Masking
DOUBLE
Status
COMPLETED
Enrollment
42
Start
2020-09-12
Primary completion
2021-05-28
Lead sponsor
Innovent Biologics (Suzhou) Co. Ltd.
Conditions
Type 2 Diabetes
Interventions
DRUG:IBI362; DRUG:Placebo; DRUG:Dulaglutide
Results posted
FALSE

Registered primary outcomes

  • To assess the number and incidence of Treatment-Emergent Adverse Events [Safety and Tolerability] of IBI362 compared with placebo [From the first dose of study drug to week 19]

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
R0009340A phase 1b randomised controlled trial of a glucagon-like peptide-1 and glucagon receptor dual agonist IBI362 (LY3305677) in Chinese patients with type 2 diabetes.
Jiang H, Nature communications
2022Randomized trialPMID 35750681DOIcites ClinicalTrials.gov:NCT04466904; registry reference DERIVED:35750681