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

Phase 3

Completed

• Conditions: Androgenetic Alopecia; Female Pattern Hair Loss
• Interventions: Drug: minoxidil

• Registration Number: NCT00958750
• Lead Sponsor: Charite University, Berlin, Germany

Brief Summary

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2008-06
• Primary Completion: 2009-02
• Study Completion: 2009-06
• Status Verified: 2009-08
• Study First Submitted: 2009-08-12
• Study First Submitted QC: 2009-08-12
• Study First Posted: 2009-08-13
• Last Update Submitted: 2011-11-17
• Last Update Posted: 2011-11-18

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 113

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
5% MTF	minoxidil	5% minoxidil topical foam used once daily
2% MTS	minoxidil	2% minoxidil topical solution twice daily use

Primary Outcome Measures

Name	Time	Method
Change of target area non-vellus hair count (TAHC) [n/cm²] after 24 weeks	24 weeks

Secondary Outcome Measures

Name	Time	Method
Assessing the investigational products safety by means of clinical examination (local intolerance, facial hypertrichosis, AE, SAE) and blood Minoxidil level (baseline + week 24)	24 weeks
Change of cumulative hair width in non-vellus hair (TAHW) after 24 weeks	24 weeks
Global expert panel rating of change in scalp coverage via assessment of global photographs	24 weeks
Volunteer questionnaire rating for administration and contentment of the study product	24 weeks

Trial Locations

Locations (1)

Charité-Universitaetsmedizin; Clinical Research Center for Hair and Skin Science; 🇩🇪 Berlin, Germany