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NCT07431177 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study of Non-segmental Vitiligo, sponsored by Novartis Pharmaceuticals.

Recruiting
Registry status
Phase 2
Development phase
210
Enrollment target
6
Study locations

NCT07431177 is a Phase 2 study of Non-segmental Vitiligo that is actively recruiting participants, run by Novartis Pharmaceuticals. The registered enrollment target is 210 participants, above the 184-participant average among 5 other Non-segmental Vitiligo trials with a reported enrollment target (14% higher). The trial reports 6 study locations across 5 states.

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The verdict

NCT07431177, a Phase 2 study of Non-segmental Vitiligo, is actively recruiting participants, sponsored by Novartis Pharmaceuticals.

RECRUITING
Registry status
Phase 2
Development phase
210 participants
Enrollment target
6
Study locations

Study Summary

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.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG GIA632

Study Locations (6)

New South Wales

  • Novartis Investigative Site - Sydney
  • Novartis Investigative Site - Waitara

Alabama

  • Cahaba Derm and skin hlth ctr 27 - Birmingham

Florida

  • Miami Derm and Laser Institute - Miami

Michigan

  • Revival Research Institute - Troy

Ontario

  • Novartis Investigative Site - Toronto

Trial Details

FieldValue
Enrollment Target 210 participants
Start Date 2026-03-09
Est. Completion 2030-02-14
Phase Phase 2

Sponsor

Novartis Pharmaceuticals

1,375 total trials

What the Registry Record Tells You About NCT07431177

The ClinicalTrials.gov registry entry for NCT07431177 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 210 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 184-participant average among 5 other Non-segmental Vitiligo trials with a reported enrollment target (14% higher). The listed sponsor is Novartis Pharmaceuticals, which has 1,375 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Non-segmental Vitiligo appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT07431177 reports 6 study locations spanning 5 distinct geographic areas - top geographies include New South Wales, Alabama, Florida.

Frequently Asked Questions

What is clinical trial NCT07431177 about?

NCT07431177 is a clinical study titled "A Phase IIb Dose-ranging Study to Assess the Efficacy and Safety of GIA632 in Participants With Non-segmental Vitiligo". 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.

What is the current status of trial NCT07431177?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 210 participants. The study started on 2026-03-09. Estimated completion is 2030-02-14.

What conditions does trial NCT07431177 study?

This clinical trial studies the following conditions: Non-segmental Vitiligo.

What interventions are being tested in trial NCT07431177?

The interventions under investigation include: Placebo (DRUG), GIA632 (DRUG).

Who is sponsoring clinical trial NCT07431177?

This trial is sponsored by Novartis Pharmaceuticals, which has 1,375 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07431177 being conducted?

This trial has 6 study locations across Alabama, Florida, Michigan, New South Wales, Ontario. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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