LivingGLP1
Study S002751

A Randomized, Placebo-Controlled, Double-Blind, Parallel-Group Study Evaluating the Efficacy, Safety, and Pharmacokinetics of Daily Administrations of the GLP-1 Analogue ROSE-010 on Appetite and Food Intake in Overweight and Obese Subjects

Registration

Registration
NCT06621017
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
40
Start
2024-09-26
Primary completion
2025-02-27
Lead sponsor
Rose Pharma Inc
Conditions
Obesity; Overweight
Interventions
DRUG:ROSE-010 99 mcg; DRUG:Placebo; DRUG:ROSE-010 150 mcg
Results posted
TRUE
Individual participant data sharing
NO

Registered primary outcomes

  • Food Consumption [30 minutes]

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