Safety and Efficacy Study of Human Autologous Hair Follicle Cells to Treat Androgenetic Alopecia

Inclusion Criteria: 1. Male or female between the age of 18 and 55 years and in good health having evidence of mild to moderate androgenetic alopecia (AGA) involving the vertex area of the scalp. Female patients with androgenetic alopecia (AGA) characterized as vertex pattern type II or type III of the Ludwig Scale qualify for inclusion in this study. Males with androgenetic alopecia (AGA) involving the vertex area of the scalp, characterized as type III vertex- type VI on the Norwood Scale qualify for inclusion in the study. 2. Willingness to provide written informed consent for participation in the study, attend all study visits and complete all procedures required by this protocol. 3. The test areas (areas to be injected) are of uniform skin color without erythema, dark pigmentation or scars that may confound study results. 4. Willingness to forego the use cosmetic or medical products for hair loss throughout the course of the study. 5. Females must be post-menopausal for at least one year, surgically sterile, or, if of childbearing potential, using highly-effective methods of birth control. This method of contraception must be used at least 4 weeks prior to and during the entire duration of the clinical trial. Exclusion Criteria: 1. Use of any product (medication or otherwise) which interferes with the hair growth cycle. 2. Any systemic medical treatment for hair loss (for example, Finasteride, Minoxidil, Dutasteride, or antiandrogens) within the last 12 months. 3. Start of contraception treatments containing chlormadinone or cyproterone acetate within the last 12 months. 4. Women who are pregnant or nursing. 5. Presence of any medical condition that influences the hair growth cycle (for example, alopecia areata, lichen planopilaris, lupus erythematosus, severe seborrheic eczema, psoriasis capitis or tinea capitis, untreated thyroid gland disease/goiter development, auto-immune diseases, etc.). 6. Any condition that, in the investigator's opinion would impact patient safety and/or a patient's ability to complete all study related procedures (for example, psychiatric illness, drug addiction, alcoholism, etc.). 7. Infection with human immunodeficiency virus (HIV), hepatitis, or syphilis. 8. Subjects diagnosed with cancer with or without chemotherapy treatment. 9. Sudden hair loss within the last 4 months unrelated to normal seasonal hair shedding or androgenetic alopecia (AGA). 10. Subjects in the process of or having completed surgical correction of hair loss in the past 24 months. 11. Participation in a cosmetic and/or pharmaceutical research study.