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
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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