Open-label Study Evaluating the Safety and Efficacy of AGE Serum in Non-menopausal Patients on Glucagon-like Peptide-1 Agonists
Goldman, Butterwick, Fitzpatrick and Groff
Summary
The primary objective is to evaluate the safety and efficacy of a topical serum (AGE serum) in improving visible signs of aging (e.g., fine lines, wrinkles, sagging, texture, radiance) on the full face and neck.The study will be conducted in non-menopausal female and male subjects who are on glucagon-like peptide-1 (GLP-1) agonist therapy for weight loss.
Description
enrolled subjects will apply a topical serum (AGE Serum) to the full face and neck twice daily for 12 weeks. Subject follow-up visits will occur at Week 6 and Week 12. Subjects will complete assessments and participate in and standardized 2D and 3D (Visia) digital photography.
Eligibility
- Age range
- 25–50 years
- Sex
- All
- Healthy volunteers
- Yes
Inclusion Criteria: 1. Presence of mild to moderate signs of facial aging (e.g., fine lines, laxity, dull texture) based on modified Griffith scale. 2. Adult men and women aged 25-50 years. 3. Fitzpatrick skin types I-IV. 4. Current treatment with a stable dose of GLP-1 agonist medication, including Ozempic, Rybelsus, or Wegovy for at least last 6 months. 5. Must be willing to sign a photography release and ICF, and complete the entire course of the study. 6. Subjects in good general health based on the investigator's judgment and medical history. 7. Negative urine pregnancy test result at th…
Interventions
- OtherAGE Serum
AGE serum is a topical that contains a high concentration of 30% Proxylane and a synergistic blend of fruit-derived flavonoids (blueberry, pomegranate) and Cassia alata extract.
Location
- West Dermatology Research CenterSan Diego, California