Study of Telitacicept in Patients With Refractory IgA Nephropathy

NCT ID: NCT05596708

Last Updated: 2023-02-24

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: PHASE2/PHASE3
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-03-01
• Study Completion Date: 2026-09-30

Brief Summary

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.

Conditions

IgA Nephropathy

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Telitacicept treated group

Group Type: EXPERIMENTAL

Telitacicept

Intervention Type: DRUG

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

Interventions

Telitacicept

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

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Voluntarily sign the informed consent form.

2. IgA nephropathy was confirmed by pathological biopsy.

3. Age range: ≥ 18 years old, ≤ 70 years old, male or female.

4. 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.

5. Measured glomerular filtration rate or estimated GFR (using the CKD-EPI formula) > 35 mL/min/1.73 m2.

6. 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

1. Abnormal laboratory indicators of participants need to be excluded.

2. Secondary IgA nephropathy need to be excluded.

3. Specific pathologic or clinical renal disease types, and IgA nephropathy that may require hormone therapy.

4. Patients who have experienced any of the following cardiovascular and cerebrovascular events within the 12 weeks prior to screening.

5. Use of systemic corticosteroids within 3 months prior to randomization (except local, nasal inhalation, etc.)

6. Immunosuppressants were used within 3 months prior to randomization.

7. Patients requiring hospitalization for active infection or intravenous anti-infective therapy within 3 months prior to randomization.

8. Previously or currently diagnosed active tuberculosis Untreated latent tuberculosis.

9. Herpes zoster HIV antibody positive or HCV antibody positive during the screening period.

10. Those who currently have active hepatitis or have severe liver disease and medical history.

11. Patients with malignant tumors.

12. Pregnant and lactating women, and men or women with planned children during the trial period.

13. Those who could not avoid the use of nephrotoxic drugs during the trial.

14. Allergic to human biological products.

15. 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).

16. Patients deemed ineligible for the trial by the investigator.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Second Affiliated Hospital, School of Medicine, Zhejiang University

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

The Second Affiliated Hospital of Zhejiang University School of Medicine

Hangzhou, Zhejiang, China

Countries

China

Facility Contacts

Ma Kunling, PhD

Role: primary

klma@zju.edu.cn

15150515798

Other Identifiers

SZNK

Identifier Type: -

Identifier Source: org_study_id