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Clinical Trials in Egypt / NCT07563036
Recruiting Not applicable

JAK2 Expression in Androgenetic Alopecia Before and After Topical Minoxidil

NCT07563036 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2026-02-01
Last updated
2026-05-01

Condition(s) studied

Androgenetic AlopeciaAndrogenic Alopecia

Investigational drug(s) / intervention(s)

Topical Minoxidil 5% Solution →Scalp Punch BiopsyTissue JAK2 Protein Measurement by ELISA

Topical Minoxidil 5% Solution: Topical minoxidil 5% solution applied to the affected scalp areas for 12 weeks. Men will apply 1 cc twice daily and women will apply 1 cc once daily.

Scalp Punch Biopsy: Three 2 mm punch biopsies will be obtained during the study: one from the balding scalp area and one from the non-balding scalp area at baseline, and one from the balding scalp area after 12 weeks of treatment.

Tissue JAK2 Protein Measurement by ELISA: Tissue samples obtained from scalp punch biopsies will be analyzed for Janus Kinase 2 (JAK2) protein levels using ELISA at baseline and after 12 weeks of treatment.

Study summary

Androgenetic alopecia is a common form of progressive hair loss. This prospective single-arm pre-post interventional study aims to assess tissue Janus Kinase 2 (JAK2) expression in patients with androgenetic alopecia by comparing balding and non-balding scalp at baseline, and to evaluate changes in JAK2 expression in balding scalp after 3 months of topical minoxidil 5% therapy. Clinical response will be assessed using standardized trichoscopic parameters.

Eligibility

Sex
MALE
Min age
18 Years
Max age
50 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Male adults aged 18 to 50 years with androgenetic alopecia. * Mild to moderate disease severity, defined as Hamilton-Norwood scale II to V. * Patients who are treatment-naive or willing to undergo an adequate washout period for prior hair loss therapies of at least 1 month. * Willing and able to provide written informed consent. Exclusion Criteria: * Other types of hair loss, including inflammatory or scarring alopecia. * Inflammatory scalp dermatoses, such as psoriasis or seborrheic dermatitis. * Use of systemic immunosuppressants, JAK inhibitors, or systemic corticosteroids within the last 12 months. * History of severe systemic disease, including renal, cardiovascular, or hepatic disease. * Chemotherapy during the last 5 years. * Bleeding disorders.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Kasr El Aini Hospital Cairo Cairo Governorate Recruiting

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07563036 on ClinicalTrials.gov ↗ ← All trials in Egypt