A Study of Telitacicept in Subjects With Childhood-onset Systemic Lupus Erythematosus

Last updated: September 19, 2024
Sponsor: RemeGen Co., Ltd.
Overall Status: Active - Recruiting

Phase

1

Condition

Cutaneous Lupus Erythematosus

Lupus

Bone Diseases

Treatment

Telitacicept

Telitacicept 2.5 mg/kg

Clinical Study ID

NCT05687526
18C018
  • Ages 5-17
  • All Genders

Study Summary

This is a multi-center, open-label, phase 1 study.

Eligibility Criteria

Inclusion

Main Inclusion Criteria:

  1. Fulfills SLICC 2012 or 2019 EULAR/ACR classification criteria for SLE.

  2. 5-17 years of age when signing the informed consent.

  3. Suject and/or legal guardian or parent provided written informed consent.

  4. SELENA SLEDAI score ≥ 8 at screening.

  5. Serum autoantibodies (ANA and/or anti ds-DNA) tested positive at screening.

  6. Have been on a stable standard of care for SLE for at least 30 days prior torandomization.

  7. Female patients are required to be non-pregnant, non-lactating or sterile.

Exclusion

Main Exclusion Criteria:

  1. Have received Telitacicept at any time.

  2. Have received any of the following therapies within 6 months of baseline: B-celltargeted treatment, e.g., belimumab, rituximab, abatacept, other investigationalbiologicals.

  3. Have received any of the following therapies within 90 days of baseline: anti-TNF oranti-IL-6 therapy, interleukin-1 receptor antagonist, intravenous immunoglobulin (IVIG), plasmapheresis.

  4. Have received any of the following therapies within 30 days of baseline: Intravenouscyclophosphamide, non-biological investigational agents (within 30 days of baselineor 5 half-lives, whichever is longer), newly addedimmunosuppressive/immunomodulatory agent, anti-malarial, NSAID, high-dose prednisoneor equivalent (> 1.5 mg/kg/day) or any intramuscular or intravenous steroid.

  5. Have received live vaccine within 30 days of baseline.

  6. Participated in an interventional clinical trial within 6 months of screening.

  7. Active CNS lupus requiring treatment within 60 days of baseline, including seizure,psychosis, organic brain syndrome, cerebrovascular accident, cerebritis or CNSvasculitis.

  8. Currently on kidney replacement therapy (hemodialysis, peritoneal dialysis) or inneed of such therapy within 90 days of baseline.

  9. eGFR<30 mL/min/1.73m2.

  10. Acute severe nephritis.

  11. History of vital organ transplant (e.g., heart, lung, kidney, liver) orhematopoietic stem cell/marrow transplant.

  12. Significant unstable or uncontrolled acute or chronic diseases (cardiovascular,lung, hematology, gastrointestinal, liver, renal, neurologic, malignancy orinfectious disease) that could be explained by causes other than SLE.

13 Have planned surgery, laboratory abnormalities, other diseases or conditions that, in the opinion of the investigator, makes the subject unsuitable for the study.

  1. History of malignant neoplasm in the past 5 years. 15. Primary immune deficiency.
  2. Acute or chronic infections requiring treatment. 17. HIV or HCV positive. 18.Tuberculosis. 19.HBsAg/HbcAb positive. 20.HBcAb positive. 21.History of COVID-19within 4 weeks prior to screening. 22.History of hospitalization due to severeCovid-19 within 12 months prior to screening.

23.History of allergy to parenteral administration of contrast agents, human or murine proteins or monoclonal antibodies.

24.History of drug or alcohol abuse or dependence within 364 days prior to baseline.

25.Investigators believe that there are other factors that are not suitable for participating in the experiment.

Study Design

Total Participants: 12
Treatment Group(s): 2
Primary Treatment: Telitacicept
Phase: 1
Study Start date:
May 25, 2023
Estimated Completion Date:
October 31, 2025

Study Description

The purpose of this study is to evaluate the pharmacokinetics (PK) of multiple doses of Telitacicept in subjects with childhood-onset systemic lupus erythematosus (cSLE) on a background of standard of care therapy and explore the safety and efficacy of Telitacicept in patients with cSLE.

Connect with a study center

  • Children's Hospital of Capital Institute of Pediatrics

    Beijing, Beijing
    China

    Site Not Available

  • Peking Union Medical College Hospital

    Beijing, Beijing
    China

    Site Not Available

  • Children's Hospital of Chongqing Medical University

    Chongqing, Chongqing
    China

    Site Not Available

  • Henan Children's Hospital

    Zhengzhou, Henan
    China

    Site Not Available

  • Hunan Children's Hospital

    Changsha, Hunan
    China

    Active - Recruiting

  • Nanjing Children's Hospital

    Nanjing, Jiangsu
    China

    Site Not Available

  • The First Hospital of Jilin University

    Changchun, Jilin
    China

    Site Not Available

  • Xi'an Children's Hospital

    Xi'an, Shaanxi
    China

    Site Not Available

  • Children's Hospital of Fudan University

    Shanghai, Shanghai
    China

    Site Not Available

  • Chengdu Women's & Children's Central Hospital

    Chengdu, Sichuan
    China

    Active - Recruiting

  • Children's Hospital of Zhejiang University School of Medicine

    Hangzhou, Zhejiang
    China

    Active - Recruiting

  • The Second Affiliated Hospital of Wenzhou Medical University

    Wenzhou, Zhejiang
    China

    Active - Recruiting

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.