LivingGLP1
Study S002825

Zenagamtide Use for the Reduction of Risk of Major Adverse Cardiovascular Events in People With Established Atherosclerotic Cardiovascular Disease and Either Overweight or Obesity

Registration

Registration
NCT07861100
Acronym
AMBIENCE
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
QUADRUPLE
Status
NOT_YET_RECRUITING
Enrollment
8500
Start
2026-10-26
Primary completion
2030-09-16
Lead sponsor
Novo Nordisk A/S
Conditions
Cardiovascular Risk; Obesity
Interventions
DRUG:Zenagamtide; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1335-0048; OTHER:2026-525182-53

Registered primary outcomes

  • Time from randomization to first occurrence of a 4-point (P) composite major adverse cardiovascular events (MACE) endpoint consisting of: Cardiovascular (CV) death, Non-fatal MI, Non-fatal stroke, HF hospitalization or urgent HF visit [From baseline (week 0) to up to 203 weeks or longer]

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