LivingGLP1
Study S000013

A Multicenter, Randomized, Double-blind, Placebo-controlled Clinical Study to Evaluate the Efficacy and Safety of IBI362 in Participants With Mild to Moderate Hypertension Complicated by Overweight/Obesity Who Have Not Received Antihypertensive Drug Treatment

Registration

Registration
NCT07469800
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
DOUBLE
Status
RECRUITING
Enrollment
336
Start
2026-04-23
Primary completion
2026-08-01
Lead sponsor
Innovent Biologics (Suzhou) Co. Ltd.
Conditions
Overweight; Obesity; Hypertensive
Interventions
DRUG:IBI362; DRUG:Placebo
Results posted
FALSE

Registered primary outcomes

  • To evaluate the effect of IBI362 on mean sitting systolic blood pressure (msSBP) compared with placebo at Week 16 of treatment. [Week 16]

Linked records (0)

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