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NCT07533019 · ClinicalTrials.gov registry record · Phase 2

A Study of LY4005130 in Adult Participants With Non-Segmental Vitiligo

A Phase 2 study, sponsored by Eli Lilly and Company.

Recruiting
Registry status
Phase 2
Development phase
60
Enrollment target

NCT07533019 is a Phase 2 study that is actively recruiting participants, run by Eli Lilly and Company. The registered enrollment target is 60 participants.

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The verdict

NCT07533019, a Phase 2 study, is actively recruiting participants, sponsored by Eli Lilly and Company.

RECRUITING
Registry status
Phase 2
Development phase
60 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate how well LY4005130 is tolerated and what side effects may occur in participants with non-segmental vitiligo (NSV) when compared with placebo. The study drug will be administered intravenously (IV) (into a vein in the arm). Blood tests will be performed to investigate how the body processes the study drug and how the study drug affects the body. The study will last approximately 48 weeks, including screening.

Interventions

  • DRUG Placebo
  • DRUG LY4005130

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2026-04-14
Est. Completion 2027-09
Phase Phase 2

Sponsor

Eli Lilly and Company

1,341 total trials

What the Registry Record Tells You About NCT07533019

The ClinicalTrials.gov registry entry for NCT07533019 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Eli Lilly and Company, which has 1,341 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT07533019 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT07533019 about?

NCT07533019 is a clinical study titled "A Study of LY4005130 in Adult Participants With Non-Segmental Vitiligo". The purpose of this study is to evaluate how well LY4005130 is tolerated and what side effects may occur in participants with non-segmental vitiligo (NSV) when compared with placebo. The study drug will be administered intravenously (IV) (into a vein in the arm). Blood tests will be performed to in...

What is the current status of trial NCT07533019?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 60 participants. The study started on 2026-04-14. Estimated completion is 2027-09.

What interventions are being tested in trial NCT07533019?

The interventions under investigation include: Placebo (DRUG), LY4005130 (DRUG).

Who is sponsoring clinical trial NCT07533019?

This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.