A Phase 2a Trial of FOL-005 Topical Formulations to Investigate Hair Growth Potential and Safety in Healthy Male Volunteers

NCT ID: NCT04774874

Last Updated: 2021-03-01

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 209 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-06-24
• Study Completion Date: 2021-01-29

Brief Summary

This exploratory phase IIa, double blind, randomized, vehicle controlled, multicenter dose-finding trial will evaluate the safety, tolerability, and efficacy of FOL-005 topical formulation (at 0.1%, 0.5% and 1.5% strength) administered once daily (in the evening) for 16 weeks in healthy male subjects with androgenetic alopecia.

Detailed Description

This exploratory phase IIa, double blind, randomized, vehicle controlled, multicenter dose-finding trial will evaluate the safety, tolerability, and efficacy of FOL-005 topical formulation (at 0.1%, 0.5% and 1.5% strength) administered once daily (in the evening) for 16 weeks in healthy male subjects with androgenetic alopecia.

The trial will be performed at three centers in Germany. The aim of the trial is to determine the most efficacious dose of FOL-005 topical formulation based on efficacy dose trends. It is planned to randomize 220 subjects (with a ratio 1:1:1:1 FOL-005 0.1%; FOL-005 0.5%; FOL-005 1.5%; vehicle).

The trial consists of a screening period of up to three weeks and a treatment period of 16 weeks.

Eligible subjects will be randomized at Baseline (Day 1) and will apply the investigational products themselves at home once daily for 16 weeks. Subjects will return to the sites bi- weekly for check of compliance and assessment of local tolerability. At Day1, Day 84 and Day 112 subjects will be evaluated for hair growth parameters by TrichoLAB imaging. The end of the clinical trial for each individual subject is defined as the Final Visit at Day 112. In case of premature termination of a randomized subject an Early Termination (ET) visit should be performed.

Conditions

Androgenetic Alopecia

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

FOL- 005 (0.1 %)

topical formulation

Group Type: EXPERIMENTAL

Topical formulation

Intervention Type: DRUG

Topical administration on the scalp once daily for 16 weeks

FOL -005 (0.5 %)

topical formulation

Group Type: EXPERIMENTAL

Topical formulation

Intervention Type: DRUG

Topical administration on the scalp once daily for 16 weeks

FOL -005 (1.5 %)

topical formulation

Group Type: EXPERIMENTAL

Topical formulation

Intervention Type: DRUG

Topical administration on the scalp once daily for 16 weeks

Vehicle

topical formulation

Group Type: PLACEBO_COMPARATOR

Topical formulation

Intervention Type: DRUG

Topical administration on the scalp once daily for 16 weeks

Interventions

Topical formulation

Topical administration on the scalp once daily for 16 weeks

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Healthy male, aged 18-55 years

2. Skin phototype II, III and IV according to Fitzpatrick's classification (Fitzpatrick et al. 1974)

3. Androgenetic alopecia (AGA) classified according to Hamilton Norwood grade 3V, 4, 5, 5A, 5V (Hamilton, 1951)

4. Willing and able to comply with scheduled visits

5. Willing to maintain the same hair hygiene products and general hair care habits during the trial period

6. Willing to maintain the same hair length and hair color during the trial period

7. Willing to have treatment areas shaved for TrichoLAB® measurement and marked with small semi-permanent dot tattoos

8. Willing to avoid prolonged UV exposition and UV tanning beds

9. Signed written informed consent before participation in the trial.

10. Subjects with a hair length of above 1 cm

Exclusion Criteria

1. Damaged skin in or around test sites including sunburn, uneven skin tones, tattoos, scars or other disfiguration of the test sites risking to interfere with investigational evaluations

2. Any dermatological disorders of the scalp which might interfere with the application of the investigational product (IP) or examination method, such as fungal or bacterial infections, seborrheic dermatitis (except mild forms which are managed with OTC shampoos and which do not require dermatological treatment), psoriasis, eczema, folliculitis, that require chronic use of medication or scalp atrophy

3. Any skin pathology (e.g. scar, nevus) or general condition (e.g. uncontrolled thyroid diseases) that in the Investigator's opinion can interfere with the evaluation of the test areas or requires prohibited topical or systemic therapy

4. History of active hair loss due to alopecia areata, scarring alopecia, diffuse telogen effluvium or conditions other than androgenetic alopecia

5. Diabetes mellitus

6. Presence of any acute (e.g. acute infections) or chronic illness (e.g. psoriasis, atopic dermatitis, porphyria, folliculitis) or presence or history of known skin cancer that in the opinion of the Investigators might confound the results of the trial

7. History or clinical signs of keloids or hypertrophic scars

8. Immunological disorders such as alopecia areata, and systemic lupus erythematosus and other systemic known autoimmune disorders

9. Current or within the last 6 months history of severe dietary or weight changes

10. Hair transplantation at any time

11. Known sensitization to cosmetic hair dyes or hypersensitivity to any ingredients of the IP or tattoo ink.

12. Application of topical minoxidil preparation or any other topical over-the counter (OTC) or prescription medication for hair re-growth to scalp for 4 weeks or more during a 6 months period before enrollment.

13. Use of or planned use of shampoo with expected medicinal effect on the scalp (e.g. but not limited to anti-dandruff containing ketoconazole, anti-psoriatic, anti-fungal or shampoo containing urea, caffeine, acetylsalicylic acid, etc.) during the course of trial

14. Topical treatments of the scalp including corticosteroids, tacrolimus, retinoids or other treatments that may affect hair growth in the last 3 months as well as during the trial.

15. Platelet rich plasma (PRP) or any mesotherapy treatment on scalp during the last 12 months as well as during the trial.

16. Systemic therapy using retinoids, cyclosporine, beta blockers or corticosteroids within the last 6 months as well as during the trial.

17. Scalp procedures e.g. surgery, laser, light, micro-needling within the last 6 months as well as during the trial.

18. Finasterid (e.g. Propecia®) or Dutasteride intake or topical application in the last 12 months, or any systemic hair therapy medication in the last 12 months as well as during the trial.

19. Other systemic therapy which in the opinion of the Investigator might affect hair growth

20. Current or within 2 weeks prior to first dosing use of vasodilating drugs (e.g. Pentoxifyllin, nitroglycerine) or anticoagulating drugs (e.g. heparine, cumarines, new oral anticoagulants, regular intake of acetylsalicylic acid)

21. Current or within 3 months prior to first dosing use of systemic corticosteroids (nose drops, eye drops and/or inhalers are permitted) or other immunosuppressive drugs (e.g. cyclosporine A)

22. Elevated values for vital signs: blood pressure: systolic above 160 mmHg, diastolic above 95 mmHg, pulse rate: above 100 beats/min

23. Planned or scheduled subject surgery or hospitalisation during the course of the trial

24. Previously randomized in this trial (only valid for subjects included after 01JUN2020)

25. Psychiatric conditions that might limit the participation in the trial and/or that lead to the assumption that the ability to completely understand the consequences of consent is missing.

26. Subjects, who are inmates of psychiatric wards, prisons or state institutions.

27. Participation in a clinical trial with investigational medicinal products within the last 30 days prior to the Day 1 and / or during this trial.

28. Employees of the trial sites who are directly involved in this trial or employees of the Sponsor's company.

29. If in the opinion of the Investigator the subject should not participate in the trial for any reason.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: Yes

Sponsors

proDERM GmbH

INDUSTRY

Sponsor Role: collaborator

Hair and Skin Institute, Charité, Berlin, Germany

UNKNOWN

Sponsor Role: collaborator

CentroDerm GmbH

NETWORK

Sponsor Role: collaborator

Follicum AB

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Ulrike Blume-Peytavi

Role: PRINCIPAL_INVESTIGATOR

Klinik für Dermatologie, Charité-Universitätsmedizin, Berlin

Locations

ProDerm GmbH

Hamburg, , Germany

Countries

Germany

Other Identifiers

FCS-003

Identifier Type: -

Identifier Source: org_study_id