Efficacy and Safety for Rituximab Combined With Telitacicept in the Treatment of ANCA-associated Vasculitis (TTCAAVREM)

Phase 4

Recruiting

• Conditions: ANCA Associated Vasculitis
• Interventions: Other: Placebo of Telitacicept; Drug: Telitacicept

• Registration Number: NCT05962840
• Lead Sponsor: Chinese SLE Treatment And Research Group

Brief Summary

This study is a prospective, open-labelled, randomized, controlled, single-center clinical trial. The aim of this study is to investigate the remission rate of patients treated with Telitacicept combined with Rituximab in remission-induction and Telitacicept alone in remission-maintain treatment.

Detailed Description

Background: The basic theme of AAV is relapse and remission. The maintenance therapy of AAV aimed to reduce or prevent relapse is very challenge. Although many medications have been used for the maintenance of AAV, Telitacicept (a BAFF/APRIL dual-target-inhibitor, which has been proved to be effect in treatment of SLE) has not been studied yet. One study tested the efficacy of Belimumab in the maintenance therapy for AAV. When taken Rituximab as remission-induction treatment, no relapse was observed. However, the sample size of this study is small, and the Belimumab, as a BAFF inhibitor, was not been proved to have effect on APRIL.

Many experiences have been accumulated about the efficacy and safety of Telitacicept in Chinese patients with rheumatic diseases. But there is no study to show its effectiveness in the reduction of the relapse of AAV in China. In this study, we take Telitacicept as maintain treatment in AAV patients who receive Rituximab as remission-induction treatment, to verify the effectiveness of Telitacicept in maintenance therapy of AAV.

Objectives: To investigate the effectiveness of Telitacicept in reducing relapse rate by using from remission-induction treatment combined with Rituximab to maintenance treatment of AAV.

Study Design: This is a prospective, randomized, open-label, control, pilot study.

Study Timeline

• Study Start: 2023-06-29
• Status Verified: 2023-07
• Study First Submitted: 2023-07-18
• Study First Submitted QC: 2023-07-19
• Last Update Submitted: 2023-07-19
• Study First Posted: 2023-07-27
• Last Update Posted: 2023-07-27
• Primary Completion: 2026-12-31
• Study Completion: 2026-12-31

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

1. Patients age 18 to 65 years, both genders can be included.
2. Patients who are newly diagnosed or relapsing granulomatosis with polyangiitis or microscopic polyangiitis must fulfill the 2022 ACR/EULAR classification criteria of GPA or MPA.
3. Patients have severe active AAV according to the 2021 ACR/vasculitis foundation definition.
4. Patients have to be PR3-ANCA-positive at diagnosis or during the course of their disease.

Exclusion Criteria

1. Patients who had been treated with Rituximab but had to stop due to adverse events or intolerance.
2. Patients who had other autoimmune diseases.
3. Patients with severe liver dysfunction (defined as the 2-folds elevation of normal upper limit or Child grade III), heart failure or ESRD (eGFR<30ml/min).
4. Patients who are pregnant or have planned for pregnancy in next 2 years.
5. Patients with uncontrolled sever hypertension, diabetes, active bacteria or fungal infection.
6. Patients with active hepatitis virus infection as well as patients who have active mycobacteria infection.
7. Patients with malignancy.
8. Patients who are not eligible according to the judge of the principal investigators.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Placebo arm	Placebo of Telitacicept	Patients with active AAV will be treated with Rituximab and glucocorticoid to induce remission. And the placebo of Telitacicept would be given 80 mg every week subcutaneously for 12 months. Glucocorticoid would be tapered as recommended by 2022 EULAR AAV recommendation (as protocol of PEXIVAS study)
Telitacicept treatment arm	Telitacicept	Patients with active AAV will be treated with Rituximab and glucocorticoid to induce remission. And the Telitacicept would be given 80 mg every week subcutaneously for 12 months. Glucocorticoid would be tapered as recommended by 2022 EULAR AAV recommendation (as protocol of PEXIVAS study)

Primary Outcome Measures

Name	Time	Method
The time of first relapse during 24 months follow-up of two groups	from inclusion to the end of the study, 24 months in total	The time from baseline to first relapse(re-appearance of disease with a BVAS \>0) of patients during 24 months follow-up of two groups

Secondary Outcome Measures

Name	Time	Method
The time to remission of two groups	from inclusion to the end of the study, 24 months in total	The time from baseline to remission (disappearance of disease with a BVAS = 0) of patients of two groups
The time from remission to first relapse of two groups	from inclusion to the end of the study, 24 months in total	The time from remission (disappearance of disease with a BVAS = 0) to first relapse (re-appearance of disease with a BVAS \>0) of patients of two groups
The percentage of patients with sustained remission at months 12 and at months 24 of two groups	from inclusion to the end of the study, 24 months in total	The percentage of patients with sustained remission (disappearance of disease with a BVAS = 0) at months 12 and at months 24 of two groups
The percentage of patients with relapse at months 12 and at months 24 of two groups	from inclusion to the end of the study, 24 months in total	The percentage of patients with relapse (re-appearance of disease with a BVAS \>0), major relapse (re-appearance or worsening of disease with a BVAS \>0 and involvement of at least one major organ, a life-threatening manifestation, or both) and minor relapse (re-appearance of disease with a BVAS \>0 without involvement of major organ or a life-threatening manifestation) at months 12 and at months 24 of two groups
The rate of adverse events and their severity in both treatment groups during 24 months of the study period.	from inclusion to the end of the study, 24 months in total	The rate of adverse events and their severity (Severe events were defined as the adverse events of grade 3 or 4, deaths caused by any cause, cancers, side effects that necessitate hospitalization) in both treatment groups during the study period.
The percentage of patients who progress to ESRD at the end of the study	from inclusion to the end of the study, 24 months in total	The percentage of patients who progress to ESRD at the end of the study
The time of ANCA from positive to negative of two groups	from inclusion to the end of the study, 24 months in total	The time of ANCA from positive to negative of two groups
The rate of complication of AAV in both treatment groups during 24 months of the study period.	from inclusion to the end of the study, 24 months in total	The rate of complication of AAV in both treatment groups during 24 months of the study period.

Trial Locations

Locations (1)

Peking Union Medical College Hospital; 🇨🇳 Beijing, China