LivingGLP1
Study S000323

A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Phase III Study to Evaluate the Efficacy and Safety of HRS-7535 in Participants With Chronic Kidney Disease

Registration

Registration
NCT07625774
Acronym
RENEW-CKD
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
QUADRUPLE
Status
NOT_YET_RECRUITING
Enrollment
3690
Start
2026-07
Primary completion
2031-05
Lead sponsor
Shandong Suncadia Medicine Co., Ltd.
Conditions
Chronic Kidney Disease
Interventions
DRUG:HRS-7535; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
UNDECIDED

Registered primary outcomes

  • Time to first occurrence of any of the following renal composite endpoint events [Up to approximately 4.8 years]

Linked records (0)

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