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Study identifier: NCT07558603 Synced from ClinicalTrials.gov · August 04, 2026
● Not Yet Recruiting

Evaluate the Safety and Efficacy of AGE Serum in Post-menopausal Patients on Hormone Replacement Therapy Taking Glucagon-like Peptide-1 Agonist

Condition: Laxity; Skin  ·  Sponsor: Goldman, Butterwick, Fitzpatrick and Groff

PhaseNA
Planned participants50
Who can joinFemale, 45 Years to 65 Years
Healthy volunteersYes

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Andrea Pacheco  ·  858-657-1004  ·  andrea.pacheco@platinumderm.com

Always discuss trial participation with your own doctor first.

Locations (1)

West Dermatology Research CenterSan Diego, California, United States

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