LivingGLP1
Study S001901

An Active-comparator-controlled, Open-label, Parallel Group Study to Evaluate the Effect of Survodutide on Energy Expenditure and Fatty Acid Oxidation in Subjects With Obesity

Registration

Registration
NCT06745284
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
ACTIVE_NOT_RECRUITING
Enrollment
64
Start
2025-03-26
Primary completion
2027-01-08
Lead sponsor
Boehringer Ingelheim
Conditions
Obesity
Interventions
DRUG:Survodutide; DRUG:Semaglutide
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
REGISTRY:U1111-1309-3679

Registered primary outcomes

  • Absolute change in sleeping metabolic rate (SMR) (measured in a whole room calorimeter) from baseline to first visit a participant reached at least 10% weight loss [at baseline, up to 36 weeks]

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