Study of Telitacicept in Patients With Refractory IgA Nephropathy

Official title

A Single-arm, Forward-looking, Exploratory Clinical Study of Telitacicept in Patients With Refractory IgA Nephropathy

Overview

The goal of this clinical trial is to explore the effectiveness and safety of Telitacicept in adults with refractory IgA nephropathy. The main questions it aims to answer are: * To evaluate the clinical efficacy of Telitacicept in patients with refractory IgA nephropathy. * To evaluate the safety and adverse reaction of Telitacicept in patients with refractory IgA nephropathy. Participants will be subcutaneously injected with 240mg of Telitacicept once per week. Study subject: After 6 months of sequential treatment with renin-angiotensin system (RAS) blockers or glucocorticoids, patients with pathological biopsy of 0.7≥5 g/24 hours of proteinuria was confirmed as refractory IgA nephropathy.

Interventions

• Drug Telitacicept
  Telitacicept will be subcutaneously injected at a dose of 240mg per week, lasting for 104 weeks.

Primary outcome measures

• Complete clinical response [Time frame: 3-year]
• The absolute value of eGFR [Time frame: 3-year]
• Changes in 24-hour urinary protein [Time frame: 104 weeks]

Secondary outcome measures (2)

• eGFR decrease [Time frame: 3-year]
• Need for dialysis [Time frame: 3-year]

Eligibility criteria

Inclusion criteria

• Voluntarily sign the informed consent form.
• IgA nephropathy was confirmed by pathological biopsy.
• Age range: ≥ 18 years old, ≤ 70 years old, male or female.
• During the screening period, the 24-hour urine protein of Visit 1 and Visit 2 should meet at least one ≥0.75g/24h, and the 24-hour urine protein ≥ 0.75g/24h at Visit 3.
• Measured glomerular filtration rate or estimated GFR (using the CKD-EPI formula) > 35 mL/min/1.73 m2.
• Participants had received a basic regimen including ACE inhibitors/ARBs for 12 weeks prior to randomization, and the dose of ACE inhibitors/ARBs (within the maximum tolerated range) was stable for 4 weeks prior to randomization.

Exclusion criteria

• Abnormal laboratory indicators of participants need to be excluded.
• Secondary IgA nephropathy need to be excluded.
• Specific pathologic or clinical renal disease types, and IgA nephropathy that may require hormone therapy.
• Patients who have experienced any of the following cardiovascular and cerebrovascular events within the 12 weeks prior to screening.
• Use of systemic corticosteroids within 3 months prior to randomization (except local, nasal inhalation, etc.)
• Immunosuppressants were used within 3 months prior to randomization.
• Patients requiring hospitalization for active infection or intravenous anti-infective therapy within 3 months prior to randomization.
• Previously or currently diagnosed active tuberculosis Untreated latent tuberculosis.
• Herpes zoster HIV antibody positive or HCV antibody positive during the screening period.
• Those who currently have active hepatitis or have severe liver disease and medical history.
• Patients with malignant tumors.
• Pregnant and lactating women, and men or women with planned children during the trial period.
• Those who could not avoid the use of nephrotoxic drugs during the trial.
• Allergic to human biological products.
• Patients who have been given any of the clinical trial drugs 4 weeks prior to randomization or within 5 times the half-life of the experimental drug (whichever is longer).
• Patients deemed ineligible for the trial by the investigator.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

N/A

Model

Single group

Masking

Open label

Primary purpose

Treatment

Study locations

China · 1 center

• The Second Affiliated Hospital of Zhejiang University School of Medicine — Hangzhou

Identifiers

NCT: NCT05596708 · SZNK

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗