Safety and Efficacy of BiTE in Desensitization Therapy for Highly Sensitized Kidney Transplant Candidates With cPRA ≥ 90%

Phase 4Not Yet RecruitingNCT07689149

West China Hospital20 enrolled

Overview

This study is a prospective, open-label, two-arm exploratory clinical trial aimed at evaluating the safety and efficacy of Bispecific T-cell Engager (BiTE) therapies in refractory, highly sensitized kidney transplant candidates. Patients with end-stage renal disease (ESRD) who have a calculated panel reactive antibody (cPRA) ≥ 90% and have waited for a transplant for over 5 years, despite receiving standard desensitization therapies (e.g., IVIG, plasmapheresis, rituximab), will be enrolled. A total of 20 participants will be randomized in a 1:1 ratio to receive either Blinatumomab (a CD19×CD3 BiTE) or Teclistamab (a BCMA×CD3 BiTE). The primary objective is to evaluate the desensitization response rate, defined as the reduction of cPRA to \< 20% or by ≥ 50% from baseline, assessed at multiple time points up to 1 year post-treatment. Secondary objectives include assessing the safety profile (such as the incidence of Cytokine Release Syndrome \[CRS\] and neurotoxicity), the extent of CD19+ B cell depletion, and the proportion of participants who successfully undergo kidney transplantation within 1 year.

Background: Kidney transplantation is the optimal treatment for end-stage renal disease (ESRD). However, highly sensitized patients with a calculated panel reactive antibody (cPRA) ≥ 90% face significant barriers to finding a compatible donor and have a higher risk of antibody-mediated rejection (AMR). Standard desensitization protocols, primarily utilizing intravenous immunoglobulin (IVIG) and plasmapheresis (PLEX), often fail to achieve long-term reductions in human leukocyte antigen (HLA) antibodies because they do not adequately deplete memory B cells and long-lived plasma cells. Bispecific T-cell Engagers (BiTEs) such as Blinatumomab (CD19×CD3) and Teclistamab (BCMA×CD3) directly recruit endogenous T cells to eliminate B cells and plasma cells, respectively. This study investigates whether these targeted therapies can provide a deeper and more sustained desensitization for refractory transplant candidates, bridging them to a successful transplant. Study Design: This is a single-center, prospective, non-blinded, two-arm exploratory trial conducted at West China Hospital, Sichuan University. Twenty eligible patients will be enrolled and randomly assigned (1:1) via block randomization (block size of 4) to either the Blinatumomab arm or the Teclistamab arm. Interventions: Arm 1 (Blinatumomab): Administered intravenously. Cycle 1 consists of 9 µg/day for 4 consecutive days (Days 1-4). Following a 7-day interval, Cycle 2 consists of 9 µg/day for another 4 consecutive days (Days 12-15). Arm 2 (Teclistamab): Administered subcutaneously using a step-up dosing schedule to mitigate Cytokine Release Syndrome (CRS) risk. Cycle 1 involves 0.06 mg/kg on Day 1 and 0.3 mg/kg on Day 2. Following a 7-day interval, Cycle 2 involves a target dose of 1.5 mg/kg on Day 10. Study Objectives \& Endpoints: Primary Endpoint: Desensitization response rate evaluated at 1, 2, 3, 6, and 12 months post-treatment. A positive response is defined as a reduction of cPRA from \>90% to \<20% (or a ≥50% decrease from baseline), or the conversion of positive HLA antibodies to negative, or a ≥50% reduction in Mean Fluorescence Intensity (MFI) to a predefined threshold. Secondary Endpoints: Safety and tolerability, including the incidence and severity of CRS, Immune Effector Cell-Associated Neurotoxicity Syndrome (ICANS), infections, and neutropenia. Changes in peripheral blood lymphocyte subsets, with a specific focus on CD19+ B cell depletion and recovery trends. Duration of sustained low cPRA levels. Proportion of patients receiving a kidney transplant within 1 year. Safety Monitoring: Given the mechanism of action of BiTEs, strict monitoring for adverse events like CRS and ICANS is integrated into the protocol, utilizing ASTCT consensus grading standards. Treatment algorithms for managing severe events (e.g., using tocilizumab or corticosteroids) are predefined. An independent Data and Safety Monitoring Board (DSMB) consisting of multidisciplinary experts will oversee the study. The protocol includes strict stopping rules for severe toxicities, such as ≥ Grade 3 CRS/ICANS refractory to standard treatment, severe infections, or treatment-related mortality, to ensure patient safety throughout the trial.

Eligibility

Sex: ALLMin age: 18 YearsMax age: 65 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Male or female participants aged 18 to 65 years. * Diagnosis of end-stage kidney disease and being evaluated for or awaiting kidney transplantation. * Calculated panel-reactive antibody level (cPRA) ≥90% and a kidney transplant waiting time of ≥5 years. * Previous treatment with a conventional desensitization regimen based on intravenous immunoglobulin and/or plasma exchange, with or without rituximab, with traceable medical records. * Persistent cPRA ≥90% or unacceptable HLA antibodies after conventional desensitization, resulting in failure to meet the immunological criteria for kidney transplantation. * Adequate nonrenal organ function to tolerate the study treatment, including left ventricular ejection fraction \>50%, resting oxygen saturation \>94%, AST and ALT \<3 times the upper limit of normal, total bilirubin \<34.2 μmol/L, and no active infection. * Ability to understand the study procedures, provide written informed consent, and comply with study treatment and follow-up requirements. Exclusion Criteria: * Inability to understand or comply with the study protocol or follow-up schedule. * Known or suspected hereditary complement deficiency. * Clinically significant central nervous system disease, including epilepsy, psychotic disorder, organic brain syndrome, cerebrovascular accident, encephalitis, central nervous system vasculitis, or cranial neuropathy requiring intervention. * AST, ALT, or GGT \>3 times the upper limit of normal, or alkaline phosphatase or total bilirubin \>1.5 times the upper limit of normal. * Acute myocardial infarction or unstable angina within 6 months before screening, severe cardiac arrhythmia, or New York Heart Association class III or IV heart failure. * Uncontrolled acute or chronic disease unrelated to end-stage kidney disease that may impair tolerance to study treatment. * Active or uncontrolled infection requiring systemic treatment. * Human immunodeficiency virus infection or uncontrolled active hepatitis B or hepatitis C infection. * Participation in another interventional clinical study within 3 months before screening or planned concurrent participation in another interventional study. * Previous treatment with another T-cell engager or bispecific T-cell-redirecting therapy. * Known severe hypersensitivity to blinatumomab, teclistamab, or any of their excipients. * Active malignancy. * Pregnancy, breastfeeding, or planned pregnancy during the study period. * Previous bone marrow transplantation, hematopoietic stem cell transplantation, or solid-organ transplantation other than kidney transplantation. * Receipt of a live vaccine within 30 days before screening or planned receipt of a live vaccine during study treatment. * Any other clinically significant condition that, in the investigator's judgment, may increase participant risk, interfere with study procedures, or affect safety or efficacy assessments.

Outcomes

Primary Outcomes

Percentage of participants achieving the predefined composite desensitization response

A composite desensitization response is defined as meeting at least one of the following criteria: 1. cPRA decreases to \<20%; 2. cPRA decreases by ≥50% from baseline; 3. a previously positive HLA antibody becomes negative, defined as an MFI \<1,000; or 4. the MFI of a persistent HLA antibody decreases by ≥50% from baseline or reaches the prespecified threshold. The number and percentage of participants achieving the composite response will be reported at Months 1, 2, 3, 6, and 12 after treatment. (HLA class I and II antibodies and their mean fluorescence intensity will be assessed using a single-antigen bead assay. Calculated panel-reactive antibody levels will be determined based on the unacceptable HLA antigen profile. At each prespecified assessment timepoint, participants will be classified as responders or nonresponders, and the percentage of responders will be reported.)