A Phase 1 Clinical Trial of Siltuximab for the Treatment of Antibody-Mediated Rejection After Lung Transplantation
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Siltuximab, Placebo.
- Who it may be relevant to
- Registry conditions: Antibody Mediated Rejection of Lung Transplant. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
A Phase 1 Clinical Trial of Siltuximab for the Treatment of Antibody-Mediated Rejection After Lung Transplantation (Siltux-AMR)
Overview
Antibody-mediated rejection after lung transplantation commonly results in allograft failure and death in spite of current therapeutic regimens. We are testing the safety and tolerability of the addition of a novel immunosuppressive medication to routine treatment for antibody-mediated rejection. Future studies will be needed to assess efficacy if this study demonstrates safety
Detailed description
Long-term outcomes after lung transplantation remain disappointing, and the median survival is 6.7 years. Chronic lung allograft dysfunction (CLAD) is the leading cause of death beyond the first year after lung transplantation. Antibody-mediated rejection (AMR), which is increasingly recognized after lung transplantation, is caused by donor-specific antibodies (DSA) to mismatched human leukocyte antigens (HLA) and frequently results in CLAD and death. Recent multicenter studies using intensive monitoring for AMR report an incidence over 25%. Treatment for AMR has generally focused on antibody depletion and prevention of additional antibody development. Various combinations have been used including high-dose corticosteroids, intravenous immune globulin (IVIG), Rituximab, Carfilzomib, anti-thymocyte globulin (ATG), and plasma exchange (PLEX). However, there have been no randomized controlled trials to guide management, and outcomes after AMR are dismal. One-year allograft survival after AMR is approximately 50%, and 2-year survival is only 20%. IL-6, initially identified as B-cell stimulating factor 2 (BSF-2), is a pleiotropic cytokine that drives deleterious inflammatory, alloimmune, and fibrogenic responses. In conjunction with other cytokines, IL-6 is responsible for normal antibody production and is critical for the induction of follicular helper T cells as well as the production of IL-21 which regulates immunoglobulin synthesis. IL-6 is also crucial for B-cell differentiation into plasmablasts and for enhancing plasmablast survival. These characteristics make IL-6 an especially attractive cytokine to target in the management of AMR. Human studies examining the role of IL-6 signaling blockade in the management of AMR after kidney transplantation have shown promising results, even in refractory cases. Preliminary experience with use of IL-6 signaling blockade in a very small number of lung transplant recipients with AMR has been encouraging. The principal hypothesis for this study is that IL-6 signaling blockade added to routine immunosuppressive treatment for AMR will improve clinical outcomes. However, evaluating the safety of this approach is necessary before examining efficacy in larger clinical trials because infections are the most common serious adverse events associated with IL-6 signaling blockade and a common cause of death at all timepoints after lung transplantation. This study is a Phase 1 clinical trial using Siltuximab, a monoclonal antibody to IL-6, in addition to routine immunosuppressive therapy for AMR to examine safety and define the optimal dose for the treatment of AMR. The primary endpoint is safety and tolerability, and secondary endpoints include pharmacodynamics and functional biological measures relevant to AMR (e.g., DSA, cell-free DNA). Data from this trial will inform the design of a future Phase 2 clinical trial that assesses efficacy. Carefully designed and implemented clinical trials are necessary to improve outcomes after lung transplantation.
Interventions
- Drug Siltuximab
Interleukin-6 blockade - Drug Placebo
Siltuximab placebo IV
Primary outcome measures
- Incidence of CTCAE ≥ grade 3 [Time frame: From Randomization to Day 90.]
Secondary outcome measures (11)
- incidence of CTCAE ≥ grade 3 [Time frame: during a period of 180 days after randomization]
- serum high-sensitivity CRP [Time frame: Up to 90 and 180 days after randomization]
- Blood Sultiximab levels [Time frame: Up to 90 days after randomization]
- Clearance of donor specific antibodies [Time frame: From randomization to day 180]
- Infections [Time frame: Between randomization and day 180]
- Change in Forced Vital Capacity (FVC) [Time frame: between randomization and day 180]
- Change in Forced Expiratory Volume in One Second (FEV1) [Time frame: between randomization and day 180]
- Development of Chronic Lung Allograft Dysfunction [Time frame: between randomization and day 180]
- Allograft survival [Time frame: between randomization and day 180]
- Hyperuricemia [Time frame: between randomization and day 180]
- Hyperlipidemia [Time frame: between randomization and day 180]
Eligibility criteria
Inclusion criteria
- 18 years of age or older,
- Single or bilateral lung transplant recipient,
- New diagnosis of clinical definite, probable, or possible antibody-mediated rejection according to the 2016 International Society for Heart and Lung Transplantation (ISHLT) definition with plans to be treated with Carfilzomib and/or anti-thymocyte globulin,
- Admitted to the hospital for treatment of AMR,
- Donor-specific antibodies (DSA) to human leukocyte antigens (HLA) with a Mean Fluorescence Intensity (MFI) > 1000,
- Able to understand the purpose of the study and willing to participate and sign informed consent.
Exclusion criteria
- Pregnant or breast feeding,
- Airway anastomotic dehiscence on bronchoscopy,
- Thoracotomy incision dehiscence,
- Underwent lung transplantation less than 6 months before enrollment,
- Treated with rabbit anti-thymocyte globulin (ATG) for induction immunosuppression at the time of lung transplantation,
- Underwent other invasive surgical procedure less than 6 weeks before enrollment,
- History of lymphoma or hematologic malignancy,
- Treatment with IL-6 signaling blockade with 6 months of enrollment,
- Planned treatment with plasma exchange (PLEX) for AMR,
- Cancer other than non-melanoma skin cancer with disease-free period < 3 years,
- Positive respiratory virus PCR detected within 7 days of enrollment,
- Active cytomegalovirus infection within 7 days of enrollment,
- Positive respiratory culture for Mycobacterium tuberculosis, Mycobacterium abscessus, Mycobacterium chelonae, or Mycobacterium avium complex within 4 weeks of enrollment,
- Absolute neutrophil count (ANC) < 1,000 cells/mm3 at enrollment,
- Platelet count < 75,000 cells/mm3 at enrollment,
- Hemoglobin ≥ 17 g/dL at enrollment,
- ALT or AST > 2.5 times upper limit of normal at enrollment,
- Total bilirubin > 2.5 times upper limit of normal at enrollment,
- Uric acid ≥ 7 mg/dL at enrollment.
- History of gastrointestinal tract perforation,
- History of diverticulitis (diverticulosis is not an exclusion),
- Plan for surgical procedure (other than bronchoscopy) within 120 days of enrollment.
- Inability or unwillingness to give written informed consent or comply with the study protocol,
- Any condition that in the opinion of the site investigator introduces undue risk by participating in this study or impacts the quality or interpretation of the study results.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Triple blind
- Primary purpose
- Treatment
Study locations
United States · 2 centers
- Washington University School, of Medicine, Barnes-Jewish Hospital — St Louis
- University of Utah — Saint Lake City
Identifiers
NCT: NCT06990711 · SILTUX_AMR2025 · 7R61HL169189-02