A Proof-of-Concept Study to Evaluate Topical-Lingual Semaglutide in Adults With Obesity
Gila Therapeutics, Inc. · NCT07728383
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–65 · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 4
- Target enrollment
- 40
- US sites recruiting
- 1
- Study start
- June 17, 2026
- Record last updated
- July 27, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
This study investigates the Topical-Lingual (T-L) delivery of semaglutide, a GLP-1 receptor agonist (GLP-1RA), via an oral liquid emulsion formulation as a Proof-of-Concept for the T-L delivery of metabolic hormones in general. GLP-1 is a gut-derived hormone that induces satiation through hypothalamic pathways.
Being studied: Semaglutide 6 mg liquid emulsion formulation; Wegovy® (semaglutide) Tablet; Placebo liquid emulsion formulation
Conditions: Obesity & Overweight
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Body Mass Index 30 to 45
Exclusion Criteria
- Type 2 Diabetes Mellitus
- Multiple Endocrine Neoplasia Type 2
- Medullary thyroid cancer
Recruiting US locations
Clinical Research Institute of Minnesota
Minneapolis, MN 55402
Site contact: Gary D Berman, M.D. · 612-333-2200 · gdb@allergy-asthma-docs.com
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