VENEZE Peptide Factor Hair Serum Compared With Topical 2% Minoxidil for Androgenetic Alopecia (VENEZE-AGA)

Institute of Dermatology, Thailand

Status: Enrolling

Conditions: Androgenetic Alopecia (AGA)

Treatments: Other: Veneze peptide hair serum; Drug: Topical minoxidil

Study type: Interventional

Funder types: Other

Identifiers

NCT07536100

031/2568

IRB-IOD-031/2568 (Other Identifier)

Details and patient eligibility

About

This study aims to evaluate the effectiveness and tolerability of a peptide-based hair serum compared with topical minoxidil in patients with androgenetic alopecia. Participants will be randomly assigned, in a double-blind manner, to receive either the peptide hair serum or topical minoxidil. The primary objective is to assess improvement in hair growth over the study period, including changes in hair density and hair thickness. Secondary outcomes will include safety and tolerability assessments. The findings of this study may provide evidence supporting an alternative treatment option for patients with androgenetic alopecia.

Full description

Androgenetic alopecia (AGA) is a common condition affecting both men and women and can significantly impact quality of life. Topical minoxidil is a widely used treatment; however, its effectiveness varies and it may cause local adverse effects in some patients. Peptide hair serums have emerged as a potential alternative, with proposed mechanisms including stimulation of hair follicle activity and promotion of hair growth.

This study aims to evaluate the efficacy and safety of a peptide-based hair serum compared with topical minoxidil in patients with androgenetic alopecia. The primary objective is to assess improvement in hair growth, including changes in hair density and hair thickness. Secondary objectives include evaluation of safety, tolerability, and patient-reported outcomes.

This is a randomized, double-blind, parallel-group study. Eligible participants with androgenetic alopecia will be randomly assigned to receive either the peptide-based hair serum or topical minoxidil. Treatments will be administered according to the study protocol over a defined study period.

Efficacy outcomes will include quantitative assessment of hair density and hair thickness. Safety will be evaluated through monitoring of adverse events and local tolerability.

Enrollment: 80 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Male or female participants aged ≥18 years.
• Diagnosed with androgenetic alopecia (AGA): Norwood-Hamilton classification III-V in males or Ludwig classification I-II in females.
• Able to read and write for completion of study questionnaires (e.g., Patient Global Assessment, Hair Growth Questionnaire).
• Willing to comply with study procedures, including maintaining consistent hair color and hairstyle throughout the study.
• Hair length in the non-balding area (vertex surrounding area) ≥2 cm at each visit.
• Able to attend all scheduled visits during the 24-week study period.

Exclusion criteria

• Presence of unstable or uncontrolled systemic diseases that may affect hair growth or loss within 6 months prior to screening (e.g., liver, renal, thyroid, cardiovascular, neurological diseases, diabetes, anemia).
• History of malignancy within the past 5 years, except adequately treated basal cell carcinoma or squamous cell carcinoma.
• Psychiatric disorders or other conditions that may affect participant safety or compliance.
• Pregnant or breastfeeding women.

Hair and scalp-related exclusions:

• Diffuse hair thinning involving the occipital area.
• Scalp conditions or diseases affecting hair growth (e.g., tinea infection, non-AGA hair loss, psoriasis, uncontrolled seborrheic dermatitis).
• History of hair transplantation at any time or hair extensions within 6 months prior to screening.
• Use of cosmetic products for hair loss concealment within 2 weeks prior to screening.
• Use of light/laser therapy on the scalp within 3 months prior to screening.
• Use of supplements related to hair growth (e.g., zinc, biotin) within 3 months prior to screening.
• Use of hair products containing active ingredients (e.g., caffeine, peptides) within 3 months prior to screening.
• Hair procedures such as mesotherapy or stem cell injection within 3 months prior to screening.

Medication-related exclusions:

• Known hypersensitivity to study-related products or ingredients.

• Use of dutasteride within 12 months prior to screening.

• Use of systemic cytotoxic agents.

• Use of systemic glucocorticoids within 3 months prior to screening (except inhaled or topical corticosteroids not applied to the scalp).

• Use within 6 months prior to screening of:

  • Minoxidil (topical or oral)
  • Finasteride (topical or oral)
  • Anti-androgenic drugs (e.g., spironolactone, cyproterone acetate, flutamide, bicalutamide)
  • Prostaglandin analogs applied to the scalp
  • Estrogen or progesterone topical preparations
  • Tamoxifen
  • Drugs associated with hypertrichosis (e.g., cyclosporine, phenytoin)
  • Drugs associated with hair loss (e.g., valproic acid)

• Participation in another clinical trial within 1 month prior to screening or during this study.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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80 participants in 2 patient groups

VENEZE Peptide factor hair serum

Experimental group

Description:

Participants in this arm will receive the VENEZE peptide factor hair serum applied topically to the scalp for 24 weeks.

Treatment:

Other: Veneze peptide hair serum

Topical 2% minoxidil solution

Active Comparator group

Description:

Participants in this arm will receive 2% minoxidil solution applied topically to the scalp for 24 weeks.

Treatment:

Drug: Topical minoxidil