LivingGLP1
Study S002233

A Proof-of-Concept, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, Efficacy and Pharmacokinetics of Topical-Lingual Semaglutide (T-L Semaglutide) in Adults With Obesity

Registration

Registration
NCT07728383
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE4
Masking
QUADRUPLE
Status
RECRUITING
Enrollment
40
Start
2026-06-17
Primary completion
2027-05
Lead sponsor
Gila Therapeutics, Inc.
Conditions
Obesity & Overweight
Interventions
DRUG:Semaglutide 6 mg liquid emulsion formulation; DRUG:Wegovy® (semaglutide) Tablet; DRUG:Placebo liquid emulsion formulation
Results posted
FALSE
Individual participant data sharing
NO

Registered primary outcomes

  • Percent body weight change from baseline [24 weeks]

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