- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07592000
Breakthrough - T1DM and Chronic Kidney Disease
Multicenter, Phase 1/2 Pilot Study of Safety and Efficacy Assessment of Tegoprubart and Calcineurin Inhibitors- Free Immunosuppression Therapy for Pancreatic Islet Transplantation in Patients With T1DM and Chronic Kidney Disease
Single arm- subject treated with Tegoprubart and everolimus.
The purpose of this research is to gather information on the safety and effectiveness of investigational regimen containing 2 experimental components:
- An investigational drug called Tegoprubart and
- Human pancreatic islet cells
Both Tegoprubart and human pancreatic islet cells are considered investigational because they are not approved for use in the United States by the Food and Drug Administration (FDA). Participation in this research will last about 5 years.
Assess safety, tolerability, and efficacy of transplanted islet cells and immunomodulation with Tegoprubart in combination with anti-thymocyte globulin (ATG), etanercept and with everolimus in adults with brittle T1D and chronic kidney disease (stage 2-3a).
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
This study is funded by Breakthrough T1D (formerly the Juvenile Diabetes Research Foundation) and Emerald Clinical Trials will be acting as the clinical research organization (CRO) for this study, overseeing data integrity, compliance and monitoring clinical trial activity. They will help with development of all regulatory and fully supporting University of Miami.
Islet cells are the specialized cells in the pancreas that produce insulin. In this study, islet cells will be collected from the pancreas of a deceased organ donor in a special laboratory at University of Chicago and then transplanted into the body at the University of Chicago hospital. The goal of this study is to see whether these transplanted islet cells can take over insulin production for the body. The study team will evaluate how well make insulin and how well controlled blood sugar is after the transplant. Islet transplantation has been performed and continuously optimized under clinical studies at the University of Chicago for the past 20 years. During this time, several new, potentially more effective and less toxic combinations of immunosuppressive medications have been evaluated. More recently, Tegoprubart has been tested in a small number of patients with T1D and only mild kidney dysfunction, in combination with mycophenolic acid (Myfortic). Given the promising preliminary results, Tegoprubart is now being studied in pancreatic cell transplantation together with either mycophenolic acid (MPA) or everolimus as part of the immunosuppressive regimen also in patients, who were previously ineligible for islet transplantation due to more advanced kidney dysfunction.
The islet transplant procedure involves inserting a thin, flexible tube called a catheter through a small cut in the upper abdomen. A radiologist uses x-rays and ultrasound to guide the catheter into the portal vein of the liver where the islet cells are delivered. This study of islet transplantation will test to see if islet transplantation is safe and effective; performing this study will help us find if this new medication Tegoprubart, combined with either MPA or everolimus and other medication the provider has been using routinely so far, would protect sufficiently islet transplant from the destruction by the immune system, allowing to stop insulin and have improved blood glucose control. At the same time, the providers will observe if these therapies are safe and other patients participating in the study.
Because these islet cells came from another person, the immune system may recognize them as foreign and attack them. Standard immunosuppressive medicines (Anti-thymocyte globulin [ATG] or Basiliximab and Etanercept) with either MPA or everolimus will be used to help prevent the body from attacking the transplanted islet cells. Immunosuppressive medicines may also be called anti-rejection medicines. Tegoprubart will be given in combination with these standard immunosuppressive medicines to test whether the investigational drug is safe, tolerable, and efficacious. The effect of the combination of Tegoprubart with other immunosuppressant medications has not been previously tested.
Tegoprubart is a monoclonal antibody. Antibodies are Y-shaped proteins that are produced naturally by their immune system to attack and fight foreign substances that cause illness. Monoclonal antibodies are man-made proteins manufactured to serve as substitute antibodies to fight diseases. Monoclonal antibodies can restore, enhance, or mimic (copy) the immune system's attack process; they can also tone down the immune system. Tegoprubart is thought to work by dampening down our immune system so that it will be less likely to attack the transplanted cells. For other types of transplants, like kidneys, a drug called a calcineurin inhibitor is usually used to prevent rejection. That class of drugs can be toxic to islet cells. Tegoprubart is an experimental agent that is anticipated to prevent rejection without harming the islet cells. This study will test this hypothesis. Early results from a recent kidney transplant study using Tegoprubart with Myfortic show that Tegoprubart appears to be less harmful to the insulin-producing cells, the kidneys, and the nervous system compared with tacrolimus and is comparable in prevention of rejection and risk of infectious and developing blood clots in blood vessels.
The Tegoprubart for this study has been provided by Eledon Pharmaceuticals.
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 2
- Fase 1
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Alexandra Grange - Islet Cell Transplant Program Manager
- Número de teléfono: 773-702-9771
- Correo electrónico: Alexandra.Grange@bsd.uchicago.edu
Copia de seguridad de contactos de estudio
- Nombre: Minelly Escobedo
- Correo electrónico: Minelly.Escobedo@bsd.uchicago.edu
Ubicaciones de estudio
-
-
Florida
-
Miami, Florida, Estados Unidos, 33136
- Reclutamiento
- Diabetes Research Institute, University of Miami
-
Contacto:
- Camillo Ricordi, M.D
- Número de teléfono: 305-243-3781
- Correo electrónico: islet@med.miami.edu
-
Contacto:
- Natalia Padilla
- Número de teléfono: 1-305-243-5321
- Correo electrónico: islet@med.miami.edu
-
Investigador principal:
- Camillo Ricordi, M.D.
-
-
Illinois
-
Chicago, Illinois, Estados Unidos, 60637
- Reclutamiento
- The University of Chicago
-
Contacto:
- Hannah Gilkey, 000-000-0000
- Correo electrónico: hannah.gilkey@bsd.uchicago.edu
-
Investigador principal:
- Piotr Witkowski
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Participants are eligible for consideration for the study only if all of the following criteria apply at the time of screening Inclusion:
- Subjects 18-70 years of age.
- A diagnosis of T1D ≥5 years with onset of disease at <40 years of age.
- Ability to provide informed consent.
- Able to comply with study procedures, including the requirement to utilize continuous glucose monitoring (CGM).
- Involvement in appropriate diabetes management in accordance with the standard of care, using an insulin pump or multiple daily injection (MDI) insulin therapy and, unable to achieve acceptable metabolic control because of the occurrence of unexplained SHEs.
- HbA1c level 6.5% to 9.5% inclusive.
- Absence of stimulated C-peptide (<0.3 ng/mL) in response to a mixed- meal tolerance test (MMTT).
- Chronic kidney disease stage 1, 2 or 3a
Impaired awareness of hypoglycemia based on:
- IAH (HypoA-Q Impaired Awareness Subscale ≥12) and at least one level 3 SHE during the last year or
- IAH and time-below-range (<70 mg/dl) ≥4% with level 2 hypoglycemia (<54 mg/dl) ≥1% (in Diabetes Care, Jan 2025, Patrick Choudhary) or
- Clarke Score >4 or
- Recurrent SHE defined by two or more level 3 SHEs in the year prior to screening
- If female, must be surgically sterile or postmenopausal. Women of childbearing potential may be enrolled if a pregnancy test is negative at screening/baseline. Women of childbearing potential and men with partners that are of childbearing potential must agree to use 2 forms of highly effective methods of contraception from Screening, throughout the study, and while receiving immunosuppressive therapy for the functioning graft after the conclusion of the study. Contraception use must continue for 90 days after the last administration of the study drug (see Appendix 5). Male participants must refrain from donating sperm for the duration of the study and agree to not donate sperm for 90 days after last administration of the study drug.
Exclusion Criteria:
- Body mass index (BMI) >30 kg/m2.
- Weight ≤40 kg.
- Insulin requirement >60units/day or <15 units/day.
- Untreated and uncontrolled proliferative diabetic retinopathy.
- Blood pressure: systolic blood pressure (SBP) >140 mmHg or diastolic blood pressure (DBP) >90 mmHg.
- Chronic kidney disease stage 3b or above.
- Diagnosis of macroalbuminuria (ACR>300 mg/g creatinine).
- For female participants: Positive pregnancy test, presently breast-feeding, or unwillingness to use effective contraceptive measures for the duration of the study and 90 days after discontinuation. For male participants: intent to procreate during the duration of the study or within 90 days after discontinuation or unwillingness to use effective measures of contraception.
- History of malignancy except for completely resected squamous or basal cell carcinoma of the skin.
History of a thromboembolic event (TE), known hypercoagulable state, or condition requiring long-term anticoagulation:
- Participants with a history of clotted venous access not requiring long- term anticoagulation may be included at the Principal Investigator's discretion if they have no other history of TEs or known hypercoagulable state.
- Patients on aspirin are allowed.
- Receiving treatment for a medical condition requiring chronic use of systemic steroids, except for physiologic replacement for example in Addison disease.
- Presence of ongoing active infection including tuberculosis (TB), human immunodeficiency virus (HIV), hepatitis B, hepatitis C. Laboratory evidence of active infection even in the absence of clinical symptoms of infection is exclusionary.
- Invasive aspergillus, histoplasmosis or coccidioidomycosis infection within one year prior to Screening.
- Negative screen for Epstein-Barr Virus (EBV) by immunoglobulin G (IgG) determination.
- Current treatment with any immunosuppressive regimen, and treatment with biologic immune modulating agents, JAK inhibitors, S1P receptor agonists, azathioprine, 6- MP, or systemic corticosteroids.
- Baseline PRA over 40%
- Previous organ transplant (except failed pancreas or islet transplant)
- Persistent elevation of serum aspartate aminotransferase (AST) or alanine aminotransferase (ALT) value greater than 3 times the upper limit of normal (ULN); elevation of total bilirubin >1.5 ULN.
- Any history of receiving experimental cell or gene therapy. Exposure to any other experimental or investigational agent within 30 days or 5 half-lives; whichever is longer.
- History of substance abuse within the past 6 months.
- Severe cardiovascular disease characterized by any one of these conditions: a) stroke; b) recent myocardial infarction (within past 6 months); c) evidence of ischemia on functional cardiac exam within the last year; d) left ventricular ejection fraction<30%.
- Significant hyperlipidemia despite medical therapy defined as fasting low-density lipoprotein (LDL) cholesterol >130 mg/dL and/ or triglycerides >200 mg/dL.
- Baseline Hb below the lower limits of normal at the local laboratory; lymphopenia (<1,000/µL), neutropenia (<1,500/µL), or thrombocytopenia (platelets <100,000/µL). Participants with lymphopenia are allowed if the Principal Investigator determines there is no additional risk and obtains clearance from a hematologist.
- Administration of live attenuated vaccine(s) within 2 months of Screening.
- Any previous treatment with Tegoprubart or any other anti-CD40L therapy
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: TEGOPRUBART WITH EVEROLIMUS
maintenance immunosupression consists of Tegoprubart and Everolimus
|
Tegoprubart is a monoclonal antibody.
Antibodies are Y-shaped proteins that are produced naturally by the immune system to attack and fight foreign substances that cause illness.
Monoclonal antibodies are man-made proteins manufactured to serve as substitute antibodies to fight diseases.
Monoclonal antibodies can restore, enhance, or mimic (copy) the immune system's attack process; they can also tone down the immune system.
Tegoprubart is thought to work by dampening down our immune system so that it will be less likely to attack the transplanted cells.
For other types of transplants, like kidneys, a drug called a calcineurin inhibitor is usually used to prevent rejection.
That class of drugs can be toxic to islet cells.
Tegoprubart is an experimental agent that is anticipated to prevent rejection without harming the islet cells.
This study will test this hypothesis.
Human pancreatic islet cells is considered investigational because it is not approved for use in the United States by the Food and Drug Administration (FDA). Participation in this research will last about 5 years. The islet transplant procedure involves inserting a thin, flexible tube called a catheter through a small cut in the upper abdomen. A radiologist uses x-rays and ultrasound to guide the catheter into the portal vein of the liver where the islet cells are delivered. This study of islet transplantation will test to see if islet transplantation is safe and effective; performing this study will help us find if this new medication Tegoprubart, combined with either MPA or everolimus and other medication the investigators have been using routinely so far, would protect sufficiently islet transplant from the destruction by the immune system, allowing participants to stop insulin and have improved blood glucose control. |
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Number of participants who are achieved Optimal outcomes according to Igls criteria
Periodo de tiempo: 1 year post-transplant
|
Assessed by continuous glucose monitoring (CGM) for insulin independence, HbA1c<7.0 (53 mmol/mol), and no severe hypoglycemic episodes (SHE).
|
1 year post-transplant
|
|
Number of participants who are achieved Good outcomes according to Igls criteria
Periodo de tiempo: 1 year post-transplant
|
Assessed by CGM for some insulin support, improved blood glucose control from baseline (pre-transplant), and with SHE.
|
1 year post-transplant
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Number of participants who achieved insulin independence
Periodo de tiempo: 1 year post-transplant, and once a year thereafter until end of study
|
Evaluated by continuous glucose monitoring.
|
1 year post-transplant, and once a year thereafter until end of study
|
|
Number of participants with no SHE and with HbA1c ≤6.5 (48 mmol/mol)
Periodo de tiempo: From 1 year post-transplant through end of study participation, assessed annually
|
Assessed by patient reports of SHEs and HbA1c lab value.
|
From 1 year post-transplant through end of study participation, assessed annually
|
|
Number of participants with no SHE and with HbA1c ≤7.0 (53 mmol/mol)
Periodo de tiempo: From 1-year post-transplant through end of study participation, assessed annually
|
Assessed by patient reports of SHEs and HbA1c lab value.
|
From 1-year post-transplant through end of study participation, assessed annually
|
|
Number of participants with preserved renal function (maintain the same stage of CKD)
Periodo de tiempo: From 1-year post-transplant through end of study participation, assessed annually
|
Measurement will be based on the stages of Chronic Kidney Disease, the investigators will check if the patient maintains the same stage, and will upgrade the stage or downgrade Stages based on eGFR.
|
From 1-year post-transplant through end of study participation, assessed annually
|
|
Number of participants who developed progression of albuminuria (no albuminuria to microalbuminuria, microalbuminuria to macroalbuminuria)
Periodo de tiempo: From 1-year post-transplant through end of study participation, assessed annually.
|
Assessed by albumin lab values in relation to pre-transplant value.
|
From 1-year post-transplant through end of study participation, assessed annually.
|
|
Number of participants with no progression of albuminuria
Periodo de tiempo: From 1-year post-transplant through end of study participation, assessed annually.
|
Assessed by albumin lab values in relation to pre-transplant value.
|
From 1-year post-transplant through end of study participation, assessed annually.
|
|
Changes in estimated glomerular filtration rate (eGFR) post-transplant.
Periodo de tiempo: 6 months and 12 months after last islet transplant
|
Assessed by eGFR lab value in relation to pre-transplant value.
|
6 months and 12 months after last islet transplant
|
Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
- Enfermedades urogenitales
- Procesos Patológicos
- Enfermedades urogenitales masculinas
- Enfermedades Renales
- Enfermedades urológicas
- Enfermedades urogenitales femeninas
- Enfermedades urogenitales femeninas y complicaciones del embarazo
- Enfermedad crónica
- Atributos de la enfermedad
- Insuficiencia renal
- Condiciones Patológicas, Signos y Síntomas
- Insuficiencia Renal Crónica
- Terapéutica
- Procedimientos quirúrgicos, operativo
- Trasplante
- Trasplante de células
- Terapia basada en células y tejidos
- Terapia biológica
- Procedimientos quirúrgicos endocrinos
- Islets of Langerhans Trasplantation
Otros números de identificación del estudio
- IRB25-1433
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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