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Clinical Trials/NCT06125405
NCT06125405
Recruiting
Phase 3

Study of the Telitacicept in Pediatric Patients With Frequently Relapsing or Steroid Dependent Nephrotic Syndrome

The Children's Hospital of Zhejiang University School of Medicine1 site in 1 country20 target enrollmentNovember 28, 2023

Overview

Phase
Phase 3
Intervention
Telitacicept
Conditions
Nephrotic Syndrome in Children
Sponsor
The Children's Hospital of Zhejiang University School of Medicine
Enrollment
20
Locations
1
Primary Endpoint
1-year relapse-free survival rate
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

The main objective is to evaluate the effectiveness of telitacicept in pediatric patients with frequently relapsing or steroid dependent nephrotic syndrome within the 52-week follow-up.

Detailed Description

Nephrotic syndrome(NS) is the most common glomerular disease in children. Approximately 45-50% of patients with nephrotic syndrome exhibit frequent relapses or are dependent on steroid therapy. Frequent relapses or steroid dependence in nephrotic syndrome have been challenging issues for clinicians. Long-term, repeated, and high-dose oral steroid use can lead to side effects such as obesity, delayed development, hypertension, diabetes, glaucoma, osteoporosis, and increased susceptibility to infections. The addition of traditional immunosuppressants such as cyclophosphamide and tacrolimus can cause severe and irreversible side effects. Therefore, exploring new drugs and their application protocols is particularly important. Telitacicept has a unique dual-target mechanism that can inhibit B cell maturation and differentiation at multiple stages, thereby inhibiting B cell activity. Clinical studies have confirmed its significant efficacy in various kidney diseases, such as lupus nephritis, IgA nephropathy, and adult recurrent minimal change nephrotic syndrome; moreover, it has good safety profiles. Therefore, through this prospective, single-center, open-label clinical trial, we aim to evaluate whether telitacicept provides superior efficacy compared to existing conventional treatment regimens for childhood frequent relapse (FR) or steroid-dependent (SD) nephrotic syndrome (NS), and assess its safety profile. Our goal is to provide an optimized treatment plan for childhood FRNS or SDNS.

Registry
clinicaltrials.gov
Start Date
November 28, 2023
End Date
October 24, 2027
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
The Children's Hospital of Zhejiang University School of Medicine
Responsible Party
Principal Investigator
Principal Investigator

Mao Jianhua

Professor

The Children's Hospital of Zhejiang University School of Medicine

Eligibility Criteria

Inclusion Criteria

  • Sensitive but frequent relapses or steroids dependence nephrotic syndrome
  • Age: 2 to 18 years old
  • Normal renal function: estimated glomerular filtration rate ≥90ml/ min/1.73m2
  • Morning urine protein \<1+ or urine protein-creatinine ratio \<0.2g/g (\<20 mg/ mmol) for 3 consecutive days and above when in enroll
  • No rituximab was used within 6 months, no tacrolimus, mycophenolate mofetil, cyclosporine A, or cyclophosphamide was used within 3 months, no ACTH was used within 3 months prior to the enrollment

Exclusion Criteria

  • Family history of nephrotic syndrome, chronic glomerulonephritis or uremia
  • Leukopenia (White Blood Cells ≤ 3.0 \* 10\^9 / L)
  • Moderate to severe anemia (hemoglobin \<9.0 g/dL)
  • Thrombocytopenia (platelet count \<100\*10\^12/L)
  • Positive Hepatitis B virus serological indicators (Hepatitis B surface antigen or / and Hepatitis B virus e antigen or / and Hepatitis B core antibody), Hepatitis C virus-positive or patients with abnormal liver function (2 or more times of alamine aminotransferase or total bilirubin was exceeded the normal value, and continued to rise for 2 weeks)
  • There are chronic active infections such as Epstein-Barrvirus, cytomegalovirus or Mycobacterium tuberculosis, and the usage of steroids and immunosuppressive agents may aggravate the state of an illness
  • Secondary nephrotic syndrome (such as purpuric nephritis, lupus nephritis, etc.)
  • Those who with hematological or endocrine system diseases as well as serious organs illness such as heart, liver or kidney
  • Those who with other autoimmune diseases or primary immunodeficiencies or tumors
  • Those who have participated in other clinical trials within three months prior to the enrollment

Arms & Interventions

Telitacicept group

Weekly administration (administration time can be within 1 week + 3 days). Body weight and dosage: for subjects with body weight greater than 10kg and less than or equal to 20kg, the dose of Telitacicept is 40mg; for subjects with body weight greater than 20kg and less than or equal to 40kg, the dose of Telitacicept is 80mg; for subjects with body weight greater than 40kg and less than or equal to 60kg, the dose of Telitacicept is 120mg; for subjects with body weight greater than or equal to 60kg, the dose of Telitacicept is 160mg. Treatment duration: 52 weeks.

Intervention: Telitacicept

Outcomes

Primary Outcomes

1-year relapse-free survival rate

Time Frame: 1-year period after enrollment

The rate of no relapse within 1 year

Secondary Outcomes

  • Relapse of nephrotic syndrome during 12 months after enrollment(1-year period after enrollment)
  • Number of relapses during 12 months follow up(1-year period after enrollment)
  • The first time to relapse(1-year period after enrollment)
  • Cumulative prednisone dosage (milligrams per kilogram per year)(1-year period after enrollment)
  • Change in hemoglobin of the patients(1-year period after enrollment)
  • Change in blood albumin of the patients(1-year period after enrollment)
  • Change in renal function of the patients(1-year period after enrollment)
  • Change in mass index (BMI) during 12-month period after enrollment(1-year period after enrollment)

Study Sites (1)

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