Actively Recruiting

All Genders
ID00315380

Longitudinal Study for Eosinophilic Granulomatosis With Polyangiitis to Discover Biomarkers of Disease Activity

Led by University of Pennsylvania · Updated on 2026-01-23

700

Participants Needed

13

Research Sites

N/A

Total Duration

On this page

Sponsors

U

University of Pennsylvania

Lead Sponsor

G

GlaxoSmithKline

Collaborating Sponsor

AI-Summary

What this Trial Is About

Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare immune disorder causing asthma, high levels of eosinophils in the blood, and inflammation of blood vessels, affecting organs like skin, lungs, nerves, and kidneys. This research aims to find new biological markers, or biomarkers, to better assess how active the disease is in people with EGPA, improving disease monitoring and future treatment development. The study involves regular visits every 6 or 12 months where participants provide blood and urine samples. Each visit includes a physical exam, medical and medication history review, and completion of questionnaires about disease activity, health status, and lifestyle habits. These procedures help researchers identify biomarkers that reflect disease severity and response to treatment. Participants will be monitored over time with repeated assessments to track disease progression and biomarker levels. Researchers will analyze these data to discover markers that can predict clinical outcomes and guide care. The study aims to improve understanding of EGPA activity and support better management for patients during times when symptoms may not be obvious.

CONDITIONS

Brief Title

Longitudinal Study for Eosinophilic Granulomatosis With Polyangiitis

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with a diagnosis of eosinophilic granulomatosis with polyangiitis
  • Parent or guardian willing to provide informed consent, if applicable
Not Eligible

You will not qualify if you...

  • Inability to give informed consent and to sign the consent form

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Monitoring

Duration - Up to 8 years

Participants undergo regular monitoring to assess disease activity through physical exams, medical history, and questionnaires. Blood and urine samples are collected to discover biomarkers associated with eosinophilic granulomatosis with polyangiitis.

Visits every 6 months or annually

Trial Site Locations

Total: 13 locations

1

University of California San Diego

San Diego, California, United States, 92122

Completed

2

National Jewish Health

Denver, Colorado, United States, 80206

Completed

3

Brigham and Women's Hospital

Boston, Massachusetts, United States, 02215

Completed

4

Mayo Clinic

Rochester, Minnesota, United States, 55905

Completed

5

Cleveland Clinic Foundation

Cleveland, Ohio, United States, 44195

Completed

6

University of Pennsylvania

Philadelphia, Pennsylvania, United States, 19104

Completed

7

University of Pittsburgh

Pittsburgh, Pennsylvania, United States, 15260

Completed

8

University of Utah

Salt Lake City, Utah, United States, 84112

Completed

9

St. Joseph's Healthcare

Hamilton, Ontario, Canada

Actively Recruiting

10

Mount Sinai Hospital

Toronto, Ontario, Canada

Completed

11

medius KLINIK KIRCHHEIM

Kirchheim unter Teck, Germany, 73230

Actively Recruiting

12

AOU Meyer IRCCS

Florence, Italy

Actively Recruiting

13

Imperial College Healthcare NHS Trust/ Imperial College London

London, United Kingdom, W12 0NN

Actively Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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Published Research Related To This Trial

Self-Reported Data and Physician-Reported Data in Patients With Eosinophilic Granulomatosis With Polyangiitis: Comparative Analysis.

Irena Doubelt, Jason M Springer, Tanaz A Kermani...

https://pubmed.ncbi.nlm.nih.gov/35612893