NonSegmental Vitiligo

4

Review clinical trials related to NonSegmental Vitiligo. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

A Study of Zasocitinib in Adults With Nonsegmental Vitiligo

Vitiligo is a long-term autoimmune condition that causes the skin to lose its color. The body's germ-fighting system (immune system) mistakenly attacks the skin cells (melanocytes) which produce the pigment that gives the skin color (melanin). This leads to the formation of patches of skin with less or no pigment (depigmentation). These patches can occur anywhere on the body. In the nonsegmental form of vitiligo, similar patches occur on both sides of the body (symmetrical patches). The main aim of this study is to learn how safe zasocitinib is, how well it works and how well it is tolerated by adults with nonsegmental vitiligo. The participants will receive the study treatment (either zasocitinib or placebo) for up to 1 year (52 weeks). The placebo looks like the zasocitinib capsule but does not have any medicine in it. Participants who receive placebo at the beginning will change to zasocitinib after about 6 months. During the study, participants will visit their study clinic 11 times.

Participants needed: 200
Trial details
Phase: Phase 2Age: 18-75Biological sex: AllType: InterventionalSponsor: TakedaUpdated: Jun 12, 2026Locations: 70
Eligibility criteria

Participant is willing and able to understand and fully comply with trial proced... [+4]

Participant has segmental vitiligo (including mixed vitiligo) or any other conge... [+54]

Status: Recruiting

Melanotan II (MT-II) as an Adjunct to NB-UVB Phototherapy for Repigmentation in Stable Nonsegmental Vitiligo

This example interventional study record describes a randomized Phase 2 clinical trial evaluating investigational Melanotan II (MT-II) as an adjunct to standard NB-UVB phototherapy for repigmentation in adults with stable nonsegmental vitiligo.

Participants needed: 60
Trial details
Phase: Phase 2Age: 18-65Biological sex: AllType: InterventionalSponsor: Hudson BiotechUpdated: Feb 27, 2026Locations: 1
Eligibility criteria

Adults aged 18-65 years able to provide informed consent. [+4]

Segmental vitiligo as the predominant type, or rapidly progressive disease withi... [+8]

Status: Recruiting

A Study to Evaluate the Safety and Efficacy of Ruxolitinib Cream in Pediatric Participants With Nonsegmental Vitiligo

The purpose of this study is to to evaluate the safety and efficacy of ruxolitinib cream in pediatric participants with nonsegmental vitiligo.

Participants needed: 180
Trial details
Phase: Phase 3Age: 2-11Biological sex: AllType: InterventionalSponsor: Incyte CorporationUpdated: Dec 18, 2025Locations: 99
Eligibility criteria

Clinical diagnosis of nonsegmental vitiligo with depigmented area including ≥ 0.... [+4]

Diagnosis of other forms of vitiligo (eg, segmental). [+13]

Status: Recruiting

A Study to Evaluate the Efficacy and Safety of Ruxolitinib Cream in Children (6 to < 12 Years Old) With Nonsegmental Vitiligo

The purpose of this study is to evaluate the efficacy and safety of ruxolitinib cream in children (6 to \< 12 years old) with nonsegmental vitiligo.

Participants needed: 250
Trial details
Phase: Phase 3Age: 6-11Biological sex: AllType: InterventionalSponsor: Incyte CorporationUpdated: Dec 17, 2025Locations: 86
Eligibility criteria

Aged 6 to < 12 years at the time of signing the ICF. [+5]

Diagnosis of other forms of vitiligo (eg, segmental). [+16]