LivingGLP1
Study S000464

Tolerability of Cagrilintide in People With Obesity That Discontinued GLP-1-RA Therapies Due to Gastrointestinal Adverse Events: a Double-blinded Randomised Feasibility Study

Registration

Registration
NCT07607587
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
QUADRUPLE
Status
RECRUITING
Enrollment
114
Start
2026-05-29
Primary completion
2027-11-19
Lead sponsor
Novo Nordisk A/S
Conditions
Obesity; Overweight
Interventions
DRUG:Cagrilintide; DRUG:Placebo (matched to Cagrilintide)
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1325-8511

Registered primary outcomes

  • Percentage of participants on standard dose or higher dose (yes/no) of cagrilintide and placebo [At week 26]

Linked records (0)

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