Promoting Repigmentation After Epidermal Cell Suspension Grafting and preVENTing the Loss of Melanocytes Using Topical Ruxolitinib for Vitiligo in Resistant Areas

NCT ID: NCT05872477

Last Updated: 2025-01-20

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 20 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-09-05
• Study Completion Date: 2025-01-10

Brief Summary

Medical approaches remain the gold standard treatment for non-segmental forms of vitiligo. Topical ruxolitinib cream has demonstrated its efficacy and good tolerance for treating vitiligo. While about 30% of patients will achieve at least 90% of repigmentation on the face after 1 year of treatment, some locations on the body, such as hands, feet, bony prominences remain highly challenging, and most patients won't get satisfactory repigmentation on those areas despite months of application of topical treatments, even when combined with UV. The poor rate of repigmentation in these locations are probably explained by the difficulty to stimulate the differentiation and proliferation of melanocytes stem cells in those areas. To study the efficacy at 3 months of epidermal cell suspension grafting followed by twice daily applications topical 1.5% ruxolitinib cream compared to epidermal cell suspension grafting followed by placebo in vitiligo resistant areas.There will be 2 arms with intra individual comparison. Both groups will receive epidermal cell suspension (provided by Cutiss®). After 7 days the dressing will be removed. Each grafted side of the body will be randomly assigned to receive twice daily application of topical 1.5% ruxolitinib cream (Group A) or twice daily application of placebo cream (Group B). After 3 months, both sides will be treated by twice daily applications of topical ruxolitinib for 3 additional months.There will be 8 visits in total during the 7 months duration for each subject.

Conditions

Vitiligo

Study Design

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

Study Groups

Group treatment

There will be 2 arms with intra individual comparison. After 7 days the dressing will be removed. Each grafted side of the body will be randomly assigned to receive twice daily application of topical 1.5% ruxolitinib cream After 3 months, both sides will be treated by twice daily applications of topical ruxolitinib for 3 additional months.

Group Type: EXPERIMENTAL

Ruxolitinib Topical

Intervention Type: DRUG

There will be 2 arms with intra individual comparison. Both groups will receive epidermal cell suspension (provided by Cutiss®). After 7 days the dressing will be removed. Each grafted side of the body will be randomly assigned to receive twice daily application of topical 1.5% ruxolitinib cream (Group A) or twice daily application of placebo cream (Group B). After 3 months, both sides will be treated by twice daily applications of topical ruxolitinib for 3 additional months.

group placebo

Each grafted side of the body will be randomly assigned to receive twice daily application of placebo cream (Group B).

After 3 months, both sides will be treated by twice daily applications of topical ruxolitinib for 3 additional months.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

There will be 2 arms with intra individual comparison. Both groups will receive epidermal cell suspension (provided by Cutiss®). After 7 days the dressing will be removed. Each grafted side of the body will be randomly assigned to receive twice daily application of topical 1.5% ruxolitinib cream (Group A) or twice daily application of placebo cream (Group B). After 3 months, both sides will be treated by twice daily applications of topical ruxolitinib for 3 additional months.

Interventions

Ruxolitinib Topical

There will be 2 arms with intra individual comparison. Both groups will receive epidermal cell suspension (provided by Cutiss®). After 7 days the dressing will be removed. Each grafted side of the body will be randomly assigned to receive twice daily application of topical 1.5% ruxolitinib cream (Group A) or twice daily application of placebo cream (Group B). After 3 months, both sides will be treated by twice daily applications of topical ruxolitinib for 3 additional months.

Intervention Type: DRUG

Placebo

There will be 2 arms with intra individual comparison. Both groups will receive epidermal cell suspension (provided by Cutiss®). After 7 days the dressing will be removed. Each grafted side of the body will be randomly assigned to receive twice daily application of topical 1.5% ruxolitinib cream (Group A) or twice daily application of placebo cream (Group B). After 3 months, both sides will be treated by twice daily applications of topical ruxolitinib for 3 additional months.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Men and women with non-segmental vitiligo.

2. ≥ 18 and <80 years.

3. At least one pair bilateral of stable vitiligo lesions with a surface >2cm² and < 20cm², located outside the face unresponsive to medical treatment

4. For women of child-bearing age, an effective contraception (estroprogestative pill, contraceptive implant, IUD, condoms or tubal ligation) should be used for more than one month before the inclusion in the study. A urine pregnancy test (βHCG in urines) will be performed.

5. Affiliation to a social security system

6. Signed informed consent

7. Participants who agree to discontinue all agents used to treat vitiligo from screening through the final safety follow-up visit.

Exclusion Criteria

1. Pregnant or breast-feeding women. Or women who plan to get pregnant during the study duration.

2. Segmental or mixed vitiligo

3. Vitiligo lesions located only on face, feet, or fingers. (dorsum of the hand accepted).

4. Concomitant use of topical or systemic immunosuppressive medication or steroids

5. Previous treatment with topical ruxolitinib cream or any systemic JAK inhibitor

6. Areas that have already received surgical grafting

7. Patients suffering from photodermatosis or taking photosensitive drugs

8. Medical history of hypertrophic scars or keloids

9. Medical history of skin cancer on the site to be treated

10. Allergy to ruxolitinib cream, xylocaine or hyaluronic acid or trypsin (Viticell® must not be utilised with patients who are hypersensitive to hyaluronic acid or trypsin)

11. Active infection

12. Patients with thromboembolic risk

13. Any dermatosis located on the treated site that could interfere with the evaluation of the treatment

14. Vulnerable people: pregnant or breast-feeding women, minors, adult under guardianship or deprived of freedom

15. Participants in other clinical therapeutic studies involving a drug that could interfere with the present evaluation

16. Participants with active acute bacterial, fungal, or viral skin infection within 1 week before baseline;

17. Participants with concurrent malignant disease or a history of that in the 5 years preceding the baseline visit except for adequately treated non metastatic malignancies;

18. Participants with current and/or history of liver disease, including known hepatitis B or C, with hepatic or biliary abnormalities;

19. Participants with current and/or history of tuberculosis;

20. Participants who have used depigmentation treatments for past treatment of vitiligo or other pigmented areas.

21. Patient under guardianship or curatorship

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Centre Hospitalier Universitaire de Nice

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Passeron Thierry, PhD

Role: PRINCIPAL_INVESTIGATOR

CHU de Nice, Service de Dermatologie

Locations

CHU de Nice - Hôpital de l'Archet

Nice, Alpes-maritimes, France

Countries

France

Other Identifiers

22-PP-16

Identifier Type: -

Identifier Source: org_study_id