LivingGLP1
Study S002530

A Double-Blind, Randomized, Multi-Center, Dose-Ranging, Phase 2 Study of the Efficacy and Safety of ALV-100 Versus Placebo for Maintenance of Weight Loss in Patients Previously Treated With Incretin-Based Therapies

Registration

Registration
NCT07837973
Acronym
PRESERVE
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
QUADRUPLE
Status
RECRUITING
Enrollment
220
Start
2026-08-10
Primary completion
2027-08-24
Lead sponsor
Alveus Therapeutics, Inc.
Conditions
Overweight , Obesity; Adults
Interventions
DRUG:ALV-100; DRUG:Placebo
Results posted
FALSE

Registered primary outcomes

  • Dose response of ALV-100 as assessed by maintenance of weight loss [24 weeks]

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