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A Phase IIb Dose-ranging Study to Assess the Efficacy and Safety of GIA632 in Participants With Non-segmental Vitiligo

Study acronym: VITESS
StatusRecruiting
PhasePhase 2
Started
View on ClinicalTrials.gov ↗

Record History

See every version on ClinicalTrials.gov ↗

  1. Minor Trial sites expanded: 76 → 83 locations
    • Eligibility criteria expanded, about 11 words
    • Secondary endpoints: details revised at 6 of 6 entries
  2. Minor Trial sites expanded: 72 → 76 locationsv17
  3. Minor Trial sites expanded: 52 → 72 locationsv16
  4. Minor Trial sites expanded: 33 → 52 locationsv15
  5. Minor Trial sites expanded: 28 → 33 locationsv14
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  1. Minor Study sites: 26 to 28v13
  2. Minor Study sites: 24 to 26v12
  3. Minor Study sites: 22 to 24
    • Primary completion date: Jun 23, 2028 to Jun 6, 2028
    • Study completion date: Feb 14, 2030 to Jan 28, 2030
    v11
  4. Minor Study sites: 20 to 22v10
  5. Minor Study sites: 18 to 20v9
  1. Minor Trial sites expanded: 15 → 18 locationsv8
  2. Minor Study sites: 13 to 15v7
  3. Minor Trial sites expanded: 10 → 13 locationsv6
  4. Minor Study sites: 8 to 10v5
  5. Minor Study sites: 6 to 8v4
  6. Minor Study sites: 3 to 6
    • Primary completion date: Jul 15, 2028 to Jun 23, 2028
    • Study completion date: Mar 8, 2030 to Feb 14, 2030
    v3
  7. Notable Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 3
    • Start date changed from estimate of Apr 1, 2026 to Mar 9, 2026
    v2
  8. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
555 trials monitored
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The main purpose of this multicenter, randomized, double-blind, placebo-controlled Phase 2b study is to investigate the safety and efficacy of GIA632 in participants with NSV and to identify the optimal dose to be promoted into the confirmatory Phase 3 program.
Trial Details
NCT Number NCT07431177
Lead Sponsor Novartis Pharmaceuticals
Conditions
(from sponsor)
Non-segmental Vitiligo
Related terms Vitiligo
Enrollment 210 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov