Evaluate the Safety and Efficacy of AGE Serum in Post-menopausal Patients on Hormone Replacement Therapy Taking Glucagon-like Peptide-1 Agonist
Part of paid clinical trials in San Diego, California.
- Sponsor
- Goldman, Butterwick, Fitzpatrick and Groff
- Study ID
- NCT07558603
- Status
- Not Yet Recruiting
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Conditions
- Laxity; Skin
Eligibility Criteria
- Sex
- FEMALE
- Age
- 45 Years - 65 Years
- Healthy Volunteers
- Accepted
Interventions
- On GLP1 plus HRT — DRUGAGE 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.
- On GLP1 Only — DRUGAGE 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.
Study Details
The primary objective is to assess the safety and efficacy of the AGE Serum in improving the appearance of skin in post-menopausal subjects on HRT and non-HRT who are takingGLP-1 agonist therapy through the use of investigator assessments, subject questionnaires/assessments, photography, skin imaging, and reported adverse reactions.
Key Dates
- Start date
- Apr 20, 2026
- Status verified
- Apr 2026
- Primary completion
- Aug 30, 2026
- Completion
- Nov 30, 2026
Study Design
- Enrollment
- 50 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Active Comparator: Group A= On GLP1 plus HRTEnrolled subjects will receive AGE Serum.
- Sham Comparator: Group B= On GLP1 OnlyEnrolled subject will receive AGE serum
Primary Outcome Measure
Modified Griffith Scale [ Time Frame: Baseline, Week 6 and Week12 ]
Central Contacts
- Andrea Pacheco858-657-1004
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| West Dermatology Research Center | San Diego | California | 92121 |
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