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Completed

NCT Number: NCT04286607

Open-Label Extension Trial of PDE4 Inhibition With Roflumilast for the Management of Plaque Psoriasis

This study will assess the safety and efficacy of ARQ-151 cream applied once a day for 24 weeks by subjects with chronic plaque psoriasis

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Key information

Age range

2 year–11 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Arcutis Biotherapeutics Clinical Site 132, Calgary, Alberta, Canada

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About this study

This is an open-label study in which ARQ-151 cream is applied once daily x 24 weeks to subjects with psoriasis

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participants legally competent to sign and give informed consent or informed consent of legal guardian, and, if age appropriate, assent by the subject, as required by local laws
  • Males and females ages 2 years and older (inclusive)
  • Subjects with chronic plaque psoriasis who meet eligibility criteria and:
  • Successfully completed a prior ARQ-151 cream study in psoriasis (Cohort 1) or
  • Are naïve to treatment with ARQ-151 cream (Cohort 2)
  • Females of childbearing potential (FOCBP) must have a negative pregnancy test at all study visits. In addition, sexually active FOCBP must agree to use at least one form of highly effective contraception throughout the trial.

Exclusion criteria

  • Subjects who experienced an ARQ-151 treatment-related AE or a serious AE (SAE) that precluded further treatment with ARQ-151 cream in a prior ARQ-151 cream study.
  • Planned excessive exposure of treated area(s) to either natural or artificial sunlight, tanning bed or other LED.
  • Females who are pregnant, wishing to become pregnant during the study, or are breast-feeding.
  • Subjects with any serious medical condition or laboratory abnormality that would prevent study participation or place the subject at significant risk, as determined by the Investigator.
  • Subjects with a history of chronic alcohol or drug abuse within 6 months of initiation of investigational product.
  • Subjects who are unable to communicate, read or understand the local language, or who display another condition, which in the Investigator's opinion, makes them unsuitable for clinical study participation.

Treatment and study plan

Topical roflumilast

Drug

Active treatment

Other names: ARQ-151 Cream 0.3%

Primary outcomes

  1. Occurrence of treatment emergent AEs (TEAEs)

    Time frame: 24 weeks

    The occurrence of TEAEs and the occurrence of (Serious Adverse Events) SAEs

Secondary outcomes

  1. Achievement of an Investigator Global Assessment (IGA) of 'clear' or 'almost clear' over time.

    Time frame: 24 weeks

  2. In subjects who achieve a 'clear' IGA time to re-starting investigational product (duration of response).

    Time frame: 24 weeks

  3. Achievement of a 50% reduction in (Psoriasis Area Severity Index) PASI over time

    Time frame: 24 weeks

  4. Achievement of a 75% reduction in PASI over time

    Time frame: 24 weeks

  5. Achievement of a 90% reduction in PASI over time

    Time frame: 24 weeks

  6. Achievement of a 100% reduction in PASI over time

    Time frame: 24 weeks

  7. Change in Worst Itch Numeric Rating Scale) WI-NRS score over time

    Time frame: 24 weeks

Sponsors and collaborators

Lead sponsor

Arcutis Biotherapeutics, Inc.

Industry

Registry information

Official study title

A Phase 3, Multicenter, Open-Label Extension Study of the Long-Term Safety of ARQ-151 Cream 0.3% in Subjects With Chronic Plaque Psoriasis

Acronym: DERMIS-OLE

Important dates

Study start
2020
Primary completion
2024
Study completion
2024
First posted
Feb 27, 2020
Registry last updated
Jan 7, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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