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Efficacy and Safety Phase II Study of VC005 Tablets in Subjects With Non-segmental Vitiligo

RecruitingPhase 2Ages 18 Years - 75 YearsAllJiangsu vcare pharmaceutical technology co., LTD
NCT07172347 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

This clinical trial is a multicenter, randomized, double-blind, controlled phase II clinical study

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📋 Eligibility rules (as published)
Inclusion Criteria: * The subject understands and voluntarily signs the informed consent form (ICF) and is willing and able to comply with the study protocol. * The subject is between 18 and 70 years of age (including borderline values) , regardless of gender. Exclusion Criteria: * Pregnant or lactating women, or subjects with pregnancy or lactation plans during the study period. * All hair in the vitiligo area on the face is white. * Those who are known or suspected to be allergic to the main ingredients and excipients of VC005 or similar drugs. * Subjects who have previously received depigmentation treatment. * Subjects who have received experimental drug administration or participated in device clinical trials within the first month or 5 half lives (whichever is longer) prior to randomization.
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What it tests

  • VC005 tablets
  • VC005 Tablets Placebo
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Where

1 site
The Peking University People's Hospital
Beijing, China
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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