Trial of Efficacy and Safety of NS-229 Versus Placebo in Patients With Eosinophilic Granulomatosis With Polyangiitis

Last updated: May 22, 2026
Sponsor: NS Pharma, Inc.
Overall Status: Active - Not Recruiting

Phase

2

Condition

Collagen Vascular Diseases

Connective Tissue Diseases

Treatment

NS-229

Placebo

Clinical Study ID

NCT06046222
NS229-P2-01
  • Ages > 18
  • All Genders

Study Summary

This study will enroll male and female subjects who are 18 years of age or older with Eosinophilic Granulomatosis With Polyangiitis.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Ability to provide written informed consent prior to participation in the study.

  • Male or female subjects aged ≥18 years at the time the informed consent form issigned.

  • Diagnosis of EGPA: Subjects who have been diagnosed with EGPA based on the historyor presence of eosinophilia plus at least a history or presence of 2 of additionalfeatures of EGPA.

  • Subjects receive background OGC dose of ≥7.5 mg/day with or without stable treatmentwith Mepolizumab/Benralizumab.

  • Use of adequate contraception.

  • Other inclusion criteria may apply.

Exclusion

Exclusion Criteria:

  • Current diagnosis of either granulomatosis with polyangiitis or microscopicpolyangiitis

  • Imminently life-threatening EGPA at the time of screening.

  • History or presence of any form of cancer within 5 years prior to screening.

  • Serious liver, renal, blood, or psychiatric disease

  • Severe or clinically significant cardiovascular disease uncontrolled with standardtreatment

  • Active systemic infections (including TB, pneumonia, Pneumocystis pneumonia, sepsis,and opportunistic infections)

  • Parasitic infection: Subjects with a known parasitic infestation within 6 monthsprior to screening.

  • HIV positive status

  • Active hepatitis due to hepatitis B virus or hepatitis C virus

  • Known history or presence of venous thromboembolism/venous thrombotic events (deepvein thrombosis and/or pulmonary embolus)

  • laboratory parameter exclusions:

  1. Estimated glomerular filtration rate of <30 mL/min/1.73 m2 by Chronic KidneyDisease Epidemiology Collaboration equations

  2. WBC count <4 × 109/L

  3. Absolute lymphocyte count <500 cells/mm3

  4. Absolute neutrophil count <1000 cells/mm3

  5. Platelet count <120,000/mm3

  6. Hemoglobin <8 g/dL (<80 g/L)

  • Subjects who are pregnant, breastfeeding, or planning to become pregnant during thetime of study participation

  • History of clinically significant drug or alcohol abuse within the last 6 months

  • Other exclusion criteria may apply.

Study Design

Total Participants: 45
Treatment Group(s): 2
Primary Treatment: NS-229
Phase: 2
Study Start date:
December 20, 2023
Estimated Completion Date:
December 31, 2026

Study Description

The purpose of this randomized, double-blind study is to investigate the efficacy and safety of NS229 compared with placebo over a 28-week study treatment period in subjects with Eosinophilic Granulomatosis with Polyangiitis (EGPA) receiving background corticosteroid therapy with or without Mepolizumab/Benralizumab therapy. During the treatment period corticosteroid dose will be tapered.

The key outcomes in the study focus on evaluation of clinical remission, defined as Birmingham Vasculitis Activity Score (BVAS)=0 with a corticosteroid dose of <=4 mg/day prednisolone/prednisone.

Connect with a study center

  • University of Alberta

    Edmonton, Alberta T6G 2B7
    Canada

    Site Not Available

  • St Joseph's Healthcare Hamilton

    Hamilton, Ontario L8N4A6
    Canada

    Site Not Available

  • University of Toronto

    Toronto, Ontario M5G 1X5
    Canada

    Site Not Available

  • CHU Nice

    Nice, 06202
    France

    Site Not Available

  • Hopital Cochin

    Paris, 75014
    France

    Site Not Available

  • Chu Rangueil

    Toulouse, 31059
    France

    Site Not Available

  • Medius Kliniken gGmbh

    Kirchheim unter Teck, Studienzentrale 73230
    Germany

    Site Not Available

  • Istituto Auxologico Italiano IRCCS

    Milan, 20145
    Italy

    Site Not Available

  • Fondazione Policlinico Universitario Campus Bio-Medico

    Roma, 00128
    Italy

    Site Not Available

  • Azienda Provinciale per i Servizi Sanitari Provincia Autonoma Trento

    Trento, 38122
    Italy

    Site Not Available

  • Azienda Ospedaliera Universitaria Integrata Verona

    Verona, 37126
    Italy

    Site Not Available

  • Chiba University Hospital

    Chuo-ku, Chiba-shi, Chiba 260-8677
    Japan

    Site Not Available

  • Hospital of the University of Occupational and Environmental Health, Japan

    Kitakyushu, Fukuoka 807-8555
    Japan

    Site Not Available

  • Hokkaido University Hospital

    Sapporo, Hokkaido 060-8648
    Japan

    Site Not Available

  • NHO Sagamihara National Hospital

    Sagamihara, Kanagawa 252-0392
    Japan

    Site Not Available

  • National Hospital Organization Yokohama Medical Center

    Yokohama, Kanagawa 245-8575
    Japan

    Site Not Available

  • Tohoku University Hospital

    Sendai, Miyagi 980-8574
    Japan

    Site Not Available

  • Osaka Habikino Medical Center

    Habikino, Osaka 583-8588
    Japan

    Site Not Available

  • Saitama Medical Center

    Kawagoe, Saitama 350-8550
    Japan

    Site Not Available

  • Juntendo University Hospital

    Bunkyo-ku, Tokyo 113-8431
    Japan

    Site Not Available

  • Kyorin University Hospital

    Mitaka, Tokyo 181-8611
    Japan

    Site Not Available

  • Toho University Omori Medical Center

    Ota-ku, Tokyo 143-8541
    Japan

    Site Not Available

  • Toho University Omori Medical Center

    Ōta-ku, Tokyo 143-8541
    Japan

    Site Not Available

  • Complejo Hospitalario Universitario de Santiago de Compostela

    Santiago de Compostela, A Coruna 15706
    Spain

    Site Not Available

  • Complejo Hospitalario de Navarra

    Pamplona, 31008
    Spain

    Site Not Available

  • Queen Elizabeth Hospital Birmingham

    Edgbaston, Birmingham B15 2GW
    United Kingdom

    Site Not Available

  • Addenbrookes Hospital

    Cambridge, CB2 2QQ
    United Kingdom

    Site Not Available

  • Royal Berkshire NHS Foundation Trust

    Reading, RG1 5AN
    United Kingdom

    Site Not Available

  • National Jewish Health

    Denver, Colorado 80206
    United States

    Site Not Available

  • Mayo Clinic

    Rochester, Minnesota 55905
    United States

    Site Not Available

  • Cleveland Clinic

    Cleveland, Ohio 44195
    United States

    Site Not Available

  • The Ohio State University Wexner Medical Center

    Columbus, Ohio 43210
    United States

    Site Not Available

  • University of Pennsylvania

    Philadelphia, Pennsylvania 19104
    United States

    Site Not Available

  • Medical University of South Carolina

    Charleston, South Carolina 29425
    United States

    Site Not Available

  • Vanderbilt University Medical Center

    Nashville, Tennessee 37232
    United States

    Site Not Available

Map preview placeholder

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.