LivingGLP1
Study S000558

A Phase 3, Randomized, Double-blinded Study to Evaluate the Efficacy and Safety of HRS-7535 Compared With Dapagliflozin in Adult Participants With Type 2 Diabetes and Inadequate Glycemic Control With Metformin (OUTSTAND-2)

Registration

Registration
NCT06589765
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
DOUBLE
Status
COMPLETED
Enrollment
810
Start
2024-09-27
Primary completion
2026-05-29
Lead sponsor
Shandong Suncadia Medicine Co., Ltd.
Conditions
Type 2 Diabetes
Interventions
DRUG:HRS-7535 tablet; DRUG:dapagliflozin tablet
Results posted
FALSE
Individual participant data sharing
UNDECIDED

Registered primary outcomes

  • Change from baseline in HbA1c at 32 weeks of treatment [at 32 weeks]

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
R0029347Oral small-molecule GLP-1RA safiglipron versus dapagliflozin in type 2 diabetes: a randomized, double-blind, active-comparator-controlled phase 3 trial.
Guo L, Nature medicine
2026Randomized trialPMID 42834229DOIcites ClinicalTrials.gov:NCT06589765; registry reference DERIVED:42834229