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ACTIVE NOT RECRUITING Phase 1

A Trial to Test the Safety and Efficacy of TEV-53408 in Treating Vitiligo

NCT06625177 · View on ClinicalTrials.gov ↗

Study Summary

The primary objective of the trial is to evaluate the safety of TEV-53408 administered subcutaneously for the treatment of adults with vitiligo. A secondary objective is to further evaluate the safety of TEV-53408. The planned study period per participant is 84 weeks including a screening period (up to 4 weeks), a 24-week open-label treatment period, a 16-week washout period, and a 40-week follow-up period.

Conditions Studied

Interventions

  • DRUG TEV-53408

Study Locations (13)

California

  • Teva Investigational Site 12044 — Fremont
  • Teva Investigational Site 12051 — Irvine
  • Teva Investigational Site 12046 — Pasadena

Texas

  • Teva Investigational Site 12045 — Dallas
  • Teva Investigational Site 12057 — Webster

Arizona

  • Teva Investigational Site 12043 — Scottsdale

Arkansas

  • Teva Investigational Site 12052 — Hot Springs

Florida

  • Teva Investigational Site 12049 — Miramar

Illinois

  • Teva Investigational Site 12047 — Chicago

Kentucky

  • Teva Investigational Site 12053 — Louisville

Michigan

  • Teva Investigational Site 12048 — Canton

Trial Details

FieldValue
Enrollment Target 38 participants
Start Date 2024-11-11
Est. Completion 2027-06-05
Phase Phase 1

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06625177

The ClinicalTrials.gov registry entry for NCT06625177 describes a study currently listed as active not recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 38 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Teva Branded Pharmaceutical Products R&D, which has 103 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Vitiligo appearing as the primary indexed condition, and to 1 intervention — of which TEV-53408 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06625177 reports 13 study locations spanning 10 distinct geographic areas — top geographies include California, Texas, Arizona. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06625177 about?

NCT06625177 is a clinical study titled "A Trial to Test the Safety and Efficacy of TEV-53408 in Treating Vitiligo". The primary objective of the trial is to evaluate the safety of TEV-53408 administered subcutaneously for the treatment of adults with vitiligo. A secondary objective is to further evaluate the safety of TEV-53408. The planned study period per participant is 84 weeks including a screening period (...

What is the current status of trial NCT06625177?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 38 participants. The study started on 2024-11-11. Estimated completion is 2027-06-05.

What conditions does trial NCT06625177 study?

This clinical trial studies the following conditions: Vitiligo. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06625177?

The interventions under investigation include: TEV-53408 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06625177?

This trial is sponsored by Teva Branded Pharmaceutical Products R&D, which has 103 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06625177 being conducted?

This trial has 13 study locations across Arizona, Arkansas, California, Florida, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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