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Efficacy of Roflumilast vs Methotrexate for Flexural and/or Genital Psoriasis

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Summary

NIH registered a Phase 2 randomized controlled trial (NCT07543640) on April 22, 2026, comparing roflumilast (500 mcg daily oral tablet) against methotrexate (standard weekly dose) for the treatment of flexural (inverse) and/or genital psoriasis over a 16-week period. The trial's primary objective is to evaluate which treatment is more effective at clearing psoriatic lesions in skin folds and genital areas and how each drug improves quality of life and pruritus symptoms. Participants will be monitored monthly for skin clearance, symptom relief, and safety/tolerability.

“This 16-week randomized controlled trial is the first to directly compare two oral medications for these specific sites: roflumilast (a daily 500 mcg pill) and methotrexate (a standard weekly dose).”

NIH , verbatim from source
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About this source

GovPing monitors ClinicalTrials.gov Studies for new healthcare & life sciences regulatory changes. Every update since tracking began is archived, classified, and available as free RSS or email alerts — 676 changes logged to date.

What changed

NIH registered a new Phase 2 clinical trial (NCT07543640) titled 'Efficacy of Roflumilast in the Treatment of Flexural and/or Genital Psoriasis: A Randomized Controlled Trial.' The trial will enroll patients with flexural (inverse/intertriginous) and/or genital psoriasis, randomly assigning them to receive either roflumilast 500 mcg daily or methotrexate weekly over 16 weeks. Participants will be monitored monthly for skin clearance, quality of life improvement, and safety/tolerability.

Affected parties include patients with topically resistant flexural or genital psoriasis seeking systemic oral treatment alternatives, and healthcare providers treating these conditions. The trial aims to provide evidence-based data on oral treatment options that do not require intensive laboratory monitoring. This registration represents standard clinical trial documentation and does not create compliance obligations for pharmaceutical manufacturers, healthcare providers, or patients beyond standard clinical research protocols.

Archived snapshot

Apr 22, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

← ClinicalTrials.gov Studies

EFFICACY OF ROFLUMILAST IN THE TREATMENT OF FLEXURAL AND/OR GENITAL PSORIASIS: A RANDOMIZED CONTROLLED TRIAL.

Phase 2 NCT07543640 Kind: PHASE2 Apr 22, 2026

Abstract

Psoriasis affecting sensitive anatomical regions, such as the skin folds (flexural or inverse psoriasis) and genitalia, presents unique therapeutic challenges. These manifestations often result in a disproportionately high burden of disease, causing significant physical discomfort and a profound negative impact on a patient's quality of life and sexual health. While topical creams are the standard first-line treatment, many patients have "topically resistant" disease that requires a systemic (oral) approach.

This 16-week randomized controlled trial is the first to directly compare two oral medications for these specific sites: roflumilast (a daily 500 mcg pill) and methotrexate (a standard weekly dose). The study's primary objective is to evaluate which treatment is more effective at clearing psoriatic lesions in the skin folds and genital area, and how each drug improves the patient's overall quality of life and symptoms like pruritus (itching).

Participants are randomly assigned to one of the two treatment groups and are monitored monthly to assess skin clearance, symptom relief, and safety/tolerability. The goal of this research is to provide patients and healthcare providers with evidence-based data on a convenient, oral treatment option that does not require intensive laboratory monitoring.

Conditions: Flexural Psoriasis (Also Known as Inverse or Intertriginous Psoriasis) and Genital Psoriasis

Interventions: Methotrexate, Roflumilast 500 Mcg Oral Tablet

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Last updated

Classification

Agency
NIH
Instrument
Notice
Branch
Executive
Legal weight
Non-binding
Stage
Final
Change scope
Minor

Who this affects

Applies to
Patients Healthcare providers Pharmaceutical companies
Industry sector
3254 Pharmaceutical Manufacturing
Activity scope
Clinical trial registration Drug efficacy study Dermatological treatment research
Geographic scope
United States US

Taxonomy

Primary area
Pharmaceuticals
Operational domain
Clinical Operations
Topics
Public Health Healthcare

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