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RECRUITING Phase 1

Maximal Usage Pharmacokinetics and Safety Study of ARQ-154 Foam 0.3% in Pediatric Participants With Scalp and Body Psoriasis

NCT07340216 · View on ClinicalTrials.gov ↗

Study Summary

This study will evaluate the systemic exposure and characterize the plasma pharmacokinetic (PK) profile and assess the safety and tolerability of ARQ-154 foam 0.3%.

Conditions Studied

Interventions

  • DRUG ARQ-154 Foam 0.3%

Study Locations (5)

Arkansas

  • Arcutis Clinical Study Site 106 — Bryant

Florida

  • Arcutis Clinical Study Site 107 — Miami Lakes

Idaho

  • Arcutis Clinical Study Site 108 — Meridian

Indiana

  • Arcutis Clinical Study Site 105 — West Lafayette

Texas

  • Arcutis Clinical Study Site 104 — Arlington

Trial Details

FieldValue
Enrollment Target 16 participants
Start Date 2025-12-15
Est. Completion 2027-02
Phase Phase 1

Sponsor

Arcutis Biotherapeutics

4 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07340216

The ClinicalTrials.gov registry entry for NCT07340216 describes a study currently listed as 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 16 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Arcutis Biotherapeutics, which has 4 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 Psoriasis appearing as the primary indexed condition, and to 1 intervention — of which ARQ-154 Foam 0.3% 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: NCT07340216 reports 5 study locations spanning 5 distinct geographic areas — top geographies include Arkansas, Florida, Idaho. 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 NCT07340216 about?

NCT07340216 is a clinical study titled "Maximal Usage Pharmacokinetics and Safety Study of ARQ-154 Foam 0.3% in Pediatric Participants With Scalp and Body Psoriasis". This study will evaluate the systemic exposure and characterize the plasma pharmacokinetic (PK) profile and assess the safety and tolerability of ARQ-154 foam 0.3%.

What is the current status of trial NCT07340216?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 16 participants. The study started on 2025-12-15. Estimated completion is 2027-02.

What conditions does trial NCT07340216 study?

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

What interventions are being tested in trial NCT07340216?

The interventions under investigation include: ARQ-154 Foam 0.3% (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07340216?

This trial is sponsored by Arcutis Biotherapeutics, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07340216 being conducted?

This trial has 5 study locations across Arkansas, Florida, Idaho, Indiana, Texas. 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