Melanotan II trials recruiting now

1 registration that name melanotan II as a study arm and are recruiting or about to, as ClinicalTrials.gov listed them on Oct 20, 2026. Read each listing for its full criteria and current status.

Kymata never assesses eligibility. Each listing names its own criteria; only its study team can say whether someone can join. Trial doses are given under the trial's monitoring and are not a schedule for anyone outside it.

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Status

All 1 registrations

RecruitingNCT07437560

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

  • Phase 2
  • Hudson Biotech
  • About 60 people
  • Started Feb 2, 2026

In plain words A Phase 2 study of melanotan II in people 18 to 65, run by Hudson Biotech. It plans to enroll about 60 people at 1 site, none in the US.

Who it lists and where

Who the trial lists, as registered

Lists people 18 to 65. Conditions: NonSegmental Vitiligo; Nonsegmental Vitiligo (Stable).

  • Adults aged 18-65 years able to provide informed consent.
  • Clinical diagnosis of nonsegmental vitiligo with stable disease (no new lesions and no lesion expansion) for >=6 months prior to screening.
  • Total body surface area involvement between 3% and 20% (inclusive), with at least two measurable target lesions suitable for standardized photography and colorimetry.
  • Willingness to undergo NB-UVB phototherapy per protocol and to avoid non-study vitiligo treatments during the study.

1 more inclusion criterion and the exclusion criteria are on the listing.

What it tests, as registered

Melanotan II (MT-II); Placebo; Narrowband UV-B (NB-UVB) phototherapy

Registered summary

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.

Where, as registered

No US site; China (1).

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