LivingGLP1
Study S003202

A Multicenter, Randomized, Double-blind, Placebo-parallel-controlled Phase III Clinical Study to Evaluate the Efficacy and Safety of Ribupatide Injection in Participants With Obesity and Knee Osteoarthritis

Registration

Registration
NCT07709910
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
QUADRUPLE
Status
NOT_YET_RECRUITING
Enrollment
382
Start
2026-07
Primary completion
2028-11
Lead sponsor
Fujian Shengdi Pharmaceutical Co., Ltd.
Conditions
Participants With Obesity and Knee Osteoarthritis
Interventions
DRUG:Ribupatide Injection; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
UNDECIDED

Registered primary outcomes

  • Change from baseline in WOMAC (Western Ontario and McMaster Universities Osteoarthritis Index) pain score after 68 weeks of treatment [after 68 weeks of continuous treatment, assessed every few weeks]
  • Percentage change from baseline in body weight after 68 weeks of treatment [after 68 weeks of continuous treatment, assessed every few weeks]

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