LivingGLP1
Study S002273

A Phase 2a Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Study to Explore the Safety and Efficacy of NT-0796 as an Adjunct to Semaglutide Plus a Reduced Calorie Diet and Increased Physical Activity in Participants With Obesity

Registration

Registration
NCT07220629
Acronym
RESOLVE-2
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
TRIPLE
Status
COMPLETED
Enrollment
82
Start
2025-10-02
Primary completion
2026-08-21
Lead sponsor
Rezera (formerly NodThera Limited)
Conditions
Obesity
Interventions
DRUG:NT-0796; DRUG:Placebo
Results posted
FALSE

Registered primary outcomes

  • Assess the safety and tolerability of NT-0796 as an adjunct to semaglutide in participants with obesity by assessing AEs and SAEs, symptoms of nausea and vomiting, clinical laboratory parameters, vital signs and ECGs. [Baseline to Week 24]

Linked records (0)

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