Efficacy and Safety Study to Compare Two Minoxidil Formulations on Women With Androgenetic Alopecia

Charité University Medicine Berlin

Status and phase

Completed

Phase 3

Conditions

Female Pattern Hair Loss

Androgenetic Alopecia

Treatments

Drug: minoxidil

Study type

Interventional

Funder types

Other

Identifiers

NCT00958750

CRC-AGA01

EudraCT: 2008-001770-33

Details and patient eligibility

About

The purpose of this study is to determine in women the risk/benefit profile and non-inferiority of a topical 5% Minoxidil foam formulation applied once daily for the treatment of androgenetic alopecia in comparison to 2% MTS used twice daily, using objective and subjective efficacy measures and safety assessments for a study period of 24 weeks.

Enrollment

113 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Female, age 18 or older, in general good health
Exhibits AGA based on a discernable decrease in hair density on the top of the scalp, relative to the sides and back of the scalp, with scalp hair density in involved area D3 to D6 on the Savin Density Scale (See Appendix 1)
Hair density equal or less than 220 hairs /cm2 measured with TrichoScan
Subjects who give their consent to the study after thoroughly clarification and who personally signed and dated the informed consent document indicating that the subject (or a legally acceptable representative), has been informed of all pertinent aspects of the trial
Women of childbearing potential, who practice an effective method of contraception for at least five consecutive weeks prior to the study entry and during the study with one of the following methods:
Double contraceptive method among hormonal contraception (e.g. contraceptive pill, intra uterine device, vaginal ring, injectable or implantable contraception), spermicide, condom and diaphragm. Oral/systemic contraception must have been the same during the past 6 months and will not be changed during the study
Sexual abstinence
Partner with a vasectomy (dated back more than 6 months) OR
Women of non-childbearing potential, i. e. postmenopausal (absence of menstrual bleeding for 2 years), or had hysterectomy, bilateral tubal ligation or bilateral ovariectomy
Women of childbearing potential must show a negative urine pregnancy test at Screening
Willing to maintain the same hairstyle, hair length and hair color throughout the study
Subjects who are willing and able to comply with scheduled visits, treatment plan, mini-tattoo, laboratory test and other trial procedures.

Exclusion criteria

Known to be hypersensitive to Minoxidil, hair dye (P-Phenylendiamin), Tattoo ink, propylene glycol, fragrances, hair gel or any vehicle components.
Current or 4 weeks dated back use of local treatment (drug or cosmetically) in the target region interfering with the study product or examination method (corticosteroids, Aminexil, Minoxidil, medical shampoos, topical estrogen, Ketoconazol)
Current or 3 months dated back use of systemic treatment (drugs or dietary supplement) taken for more than 2 consecutive weeks interfering with the study product or examination method (beta blocker, Cimetidine, Diazoxid, Isotretinoin, corticosteroids, vitamin A intake above 10000 IU per day)
Within past 6 month receiving of chemotherapy/cytotoxic agents as well as radiation and/or laser/surgical therapy of the scalp
Current or prior enrollment in any other investigational medication (drug) study within the last 4 weeks
Women with childbearing potential and insufficient contraception.
Female who is pregnant, planning a pregnancy (during the course of the study) or nursing a child
Presence of hair transplants, hair weaves or non-breathable wigs
Any dermatological disorders of the scalp in the target region with the possibility of interfering with the study product or examination method, such as fungal or bacterial infections, seborrheic dermatitis, psoriasis, eczema, folliculitis, scars or scalp atrophy
Active hair loss or history within the past 3 months including diffuse telogen effluvium, alopecia areata, scarring alopecia and androgen hair loss /hyper-androgenemia)
Other severe, acute or chronic medical condition that may lead to hair loss or interfere with the interpretation of trial results
Individuals who are institutionalized by court or regulatory order