LivingGLP1
Study S001941

A Phase 3, Multi-center, Open-label, Randomized Study to Evaluate the Efficacy and Safety of XW003 Versus Dulaglutide in Patients With T2DM Inadequately Controlled by Metformin

Registration

Registration
NCT05680129
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
NONE
Status
COMPLETED
Enrollment
623
Start
2023-01-10
Primary completion
2024-07-03
Lead sponsor
Hangzhou Sciwind Biosciences Co., Ltd.
Conditions
T2DM; Type 2 Diabetes Mellitus
Interventions
DRUG:Ecnoglutide high dosage; DRUG:Ecnoglutide low dosage; DRUG:Dulaglutide; DRUG:Metformin
Results posted
FALSE
Individual participant data sharing
NO

Registered primary outcomes

  • Change from baseline in HbA1c [Baseline, week 32]

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
R0006211Efficacy and safety of cAMP-biased GLP-1 receptor agonist ecnoglutide versus dulaglutide in patients with type 2 diabetes and elevated glucose concentrations on metformin monotherapy (EECOH-2): a 52-week, multicentre, open-label, non-inferiority, randomised, phase 3 trial.
He Y, The lancet. Diabetes & endocrinology
2025Randomized trialPMID 40854315DOIcites ClinicalTrials.gov:NCT05680129; registry reference DERIVED:40854315