Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING Phase 3

A Long-term Study of the Medicine Called Abrocitinib in Children Aged 2 Years and Older With Moderate to Severe Eczema

NCT06807281 · View on ClinicalTrials.gov ↗

Study Summary

This 24-month study will assess the long-term safety and efficacy of liquid abrocitinib oral suspension with or without topical medications in children 2 years of age or older with moderate-to-severe atopic dermatitis. The study will enroll two groups: participants who have completed other abrocitinib studies and participants who have never participated in abrocitinib studies.

Conditions Studied

Interventions

  • DRUG Abrocitinib

Study Locations (20)

Other

  • Xinhua Hospital Affiliated to Shanghai JiaoTong University School of Medicine — Shanghai
  • Fukuoka National Hospital — Fukuoka
  • Servicios Hospitalarios de Mexico S.A. DE C.V. — Chihuahua City

California

  • Investigational Drug Service - Rady Childrens Hospital-San Diego — San Diego
  • University of California, San Diego/ Rady Children's Hospital - San Diego — San Diego

Alabama

  • Cahaba Dermatology & Skin Health Center — Birmingham

Arkansas

  • Arkansas Research Trials — North Little Rock

Florida

  • Solutions Through Advanced Research — Jacksonville

Indiana

  • Dawes Fretzin Clinical Research Group, LLC — Indianapolis

South Carolina

  • Tribe Clinical Research, LLC — Greenville

North Rhine-Westphalia

  • Universitätsklinikum Münster — Münster

Trial Details

FieldValue
Enrollment Target 500 participants
Start Date 2025-12-02
Est. Completion 2032-02-22
Phase Phase 3

Sponsor

Pfizer

769 total trials

Interested in This Trial?

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06807281

The ClinicalTrials.gov registry entry for NCT06807281 describes a study currently listed as recruiting. It is categorized as Phase 3, 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 500 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pfizer, which has 769 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 Atopic Dermatitis appearing as the primary indexed condition, and to 1 intervention — of which Abrocitinib 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: NCT06807281 reports 20 study locations spanning 17 distinct geographic areas — top geographies include Other, California, Alabama. 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 NCT06807281 about?

NCT06807281 is a clinical study titled "A Long-term Study of the Medicine Called Abrocitinib in Children Aged 2 Years and Older With Moderate to Severe Eczema". This 24-month study will assess the long-term safety and efficacy of liquid abrocitinib oral suspension with or without topical medications in children 2 years of age or older with moderate-to-severe atopic dermatitis. The study will enroll two groups: participants who have completed other abrocitin...

What is the current status of trial NCT06807281?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 500 participants. The study started on 2025-12-02. Estimated completion is 2032-02-22.

What conditions does trial NCT06807281 study?

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

What interventions are being tested in trial NCT06807281?

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

Who is sponsoring clinical trial NCT06807281?

This trial is sponsored by Pfizer, which has 769 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06807281 being conducted?

This trial has 20 study locations across Alabama, Arkansas, California, Florida, Indiana. 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