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NCT04811131 · ClinicalTrials.gov registry record · Phase 2

Safety and Efficacy of ARQ-252 Cream 0.3% in Subjects With Non-Segmental Facial Vitiligo

A Phase 2 study, sponsored by Arcutis Biotherapeutics.

Terminated
Registry status
Phase 2
Development phase
114
Enrollment target

NCT04811131: Clinical Trial Phase 2 study, sponsored by Arcutis Biotherapeutics.

NCT04811131 is a Phase 2 study that was terminated before completion, run by Arcutis Biotherapeutics. The registered enrollment target is 114 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (14% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04811131, a Phase 2 study, was terminated before completion, sponsored by Arcutis Biotherapeutics.

TERMINATED
Registry status
Phase 2
Development phase
114 participants
Enrollment target

Study Summary

This study will assess the safety and efficacy of ARQ-252 cream in combination with NB-UVB phototherapy treatment in individuals with non-segmental facial vitiligo.

Primary Outcome

Achievement of F-VASI75 was declared with a ≥75% improvement from Baseline in F-VASI. F-VASI measures the % of vitiligo involvement (percentage of body surface area \[BSA\]) and the degree of depigmentation: 0% (none), 10% (only specks), 25% (pigmented area \> depigmented area), 50% (depigmented and pigmented areas equal), 75% (depigmented area \> pigmented area), 90% (specks of pigment), or 100% (no pigment). F-VASI was then derived by multiplying the values assessed for the vitiligo involvemen

Interventions

  • DRUG ARQ-252 cream 0.3%
  • DRUG ARQ-252 Vehicle cream
  • DEVICE NB-UVB phototherapy active treatment
  • DEVICE NB-UVB phototherapy sham treatment

Trial Details

FieldValue
Enrollment Target 114 participants
Start Date 2021-03-04
Est. Completion 2021-08-09
Phase Phase 2
Arcutis Biotherapeutics

25 total trials

Why NCT04811131 stopped before completion

NCT04811131 is an interventional study that assigns participants to a tested intervention. The registered 114 participants enrollment target is mid-sized for trials with a published cap, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (14% lower).

The record links to 0 conditions, and to 4 interventions - of which ARQ-252 cream 0.3% is the first listed.

NCT04811131 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04811131 about?

NCT04811131 is a clinical study titled "Safety and Efficacy of ARQ-252 Cream 0.3% in Subjects With Non-Segmental Facial Vitiligo". This study will assess the safety and efficacy of ARQ-252 cream in combination with NB-UVB phototherapy treatment in individuals with non-segmental facial vitiligo.

What is the current status of trial NCT04811131?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 114 participants. The study started on 2021-03-04. Estimated completion is 2021-08-09.

What interventions are being tested in trial NCT04811131?

The interventions under investigation include: ARQ-252 cream 0.3% (DRUG), ARQ-252 Vehicle cream (DRUG), NB-UVB phototherapy active treatment (DEVICE), NB-UVB phototherapy sham treatment (DEVICE).

Who is sponsoring clinical trial NCT04811131?

This trial is sponsored by Arcutis Biotherapeutics, which has 25 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04811131's enrollment target sits among peer trials

114 627th of 2000 higher than 1,370 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT04811131, the US trial registry maintained by the National Library of Medicine. NCT04811131 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.