LivingGLP1
Study S002557

A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy and Safety of CIN-102 (Deudomperidone) in Adult Subjects With Diabetic Gastroparesis

Registration

Registration
NCT05832151
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
382
Start
2023-03-27
Primary completion
2025-11-14
Lead sponsor
CinDome Pharma, Inc.
Conditions
Diabetic Gastroparesis
Interventions
DRUG:CIN-102 Dose 15mg or 10mg; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
NO

Registered primary outcomes

  • Effect of CIN-102 to significantly decrease gastroparesis-related symptoms as compared to baseline based on the composite of the average ANMS GCSI-DD Nausea Sub-Scale and Vomiting Scores [Over the last 2 weeks of the 12-week Treatment Period as compared to baseline]

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