Cette page a été traduite automatiquement et l'exactitude de la traduction n'est pas garantie. Veuillez vous référer au version anglaise pour un texte source.

Innocuité, tolérance et efficacité de l'immunomodulation avec A en association avec des cellules d'îlots transplantées chez les adultes atteints de diabète sucré fragile de type 1 (DT1) (Tegoprubart)

17 septembre 2026 mis à jour par: University of Chicago

Une étude pilote évaluant l'innocuité de l'utilisation d'un anticorps monoclonal contre le ligand du cluster de différenciation 40 (CD40) pour obtenir un régime d'immunosuppression sans inhibiteur de la calcineurine chez les patients atteints de diabète sucré de type 1 (DT1) et d'hypoglycémie problématique subissant une transplantation de cellules d'îlots

Tegoprubart (AT-1501) is a monoclonal antibody. Antibodies are Y-shaped proteins that are produced naturally by the subject's 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 (AT-1501) is thought to work by dampening down the immune system so that it will be less likely to attack the transplanted cells. For other types of transplants, like kidney, a drug called a calcineurin inhibitor is usually used to prevent rejection. That class of drugs can be toxic to islet cells. Tegoprubart (AT-1501) is an experimental agent that is anticipated to prevent rejection without harming the islet cells.

Aperçu de l'étude

Description détaillée

By doing this study, the study team is studying an investigational regimen containing 2 experimental components:

  • An investigational drug called AT-1501 and
  • Human pancreatic islet cells

Both Tegoprubart (AT-1501) and human pancreatic islet cells are considered investigational because they are not currently approved for use in the United States.

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 and transplanted into the body. The goal of this study is to see whether these transplanted islet cells can take over insulin production. The study team will evaluate how well the subject makes insulin and how well-controlled blood sugar is after the transplant.

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.

Because these islet cells come from another person, the subject's immune system may recognize them as foreign and attack them. Standard immunosuppressive medicines (Anti-thymocyte globulin [ATG] or Basiliximab, mycophenolate mofetil/mycophenolate sodium (MMF/MPS) (CellCept®), and Etanercept) will be used to help prevent the body from attacking the transplanted islet cells. Tegoprubart (AT-1501) 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 (AT-1501) with other immunosuppressant medications has not been previously tested.

Type d'étude

Interventionnel

Inscription (Estimé)

70

Phase

  • Phase 2
  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

    • Illinois
      • Chicago, Illinois, États-Unis, 60637
        • University of Chicago

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans à 65 ans (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  1. Men and women 18-65 years of age.

  2. A diagnosis of T1D ≥5 years with onset of disease at <40 years of age.

  3. Ability to provide informed consent.

  4. Able to comply with study procedures, including the requirement to utilize continuous glucose monitoring (CGM).

  5. Involvement in appropriate diabetes management in accordance with the standard of care, as directed by an endocrinologist or diabetologist with at least 4 (quarterly) clinical evaluations within the 12 months prior to Screening; using CGM*: using an insulin pump or multiple daily injection (MDI) of insulin therapy; and, unable to achieve acceptable metabolic control because of the occurrence of unexplained SHEs- at least 3 unexplained SHEs not secondary to a missed meal or dosing error, in the 12 months prior to Screening.

    *CGM will be provide to subjects who otherwise qualify for study participation but have not used CGM previously.

  6. At least 3 unexplained SHEs not secondary to a missed meal or dosing error, in the 12 months prior to Screening.

  7. HbA1c level 6.5% (48 mmol/mol) to 9.5% (80 mmol/mol), inclusive.

  8. Absence of stimulated C-peptide (<0.3 ng/mL) in response to a 240-minute mixed- meal tolerance test (MMTT).

  9. Impaired awareness of hypoglycemia (IAH) as defined by a Clarke Score [Clarke 1995] of 4 or more at the time of Screening, during the Screening period, and within the last 6 months prior to the transplant.

  10. If female, must be surgically sterile or 2 years postmenopausal. Women of childbearing potential may be enrolled if a serum 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.

  11. Patients with Coronavirus Disease 2019 (COVID-19) Polymerase chain reaction (PCR) negative test result at the time of Thymoglobulin infusion.

Exclusion Criteria:

  1. Any previous solid organ or islet allotransplant.

  2. Body mass index (BMI) >30 kg/m2.

  3. Weight ≤50 kg.

  4. Insulin requirement >1.0 unit/kg/day or <15 units/day.

  5. Uncontrolled proliferative diabetic retinopathy.

  6. Blood pressure: systolic blood pressure (SBP) >140 mmHg or diastolic blood pressure (DBP) >90 mmHg.

  7. Estimated glomerular filtration rate (eGFR) calculated by the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation <60 mL/min/1.73 m2.

  8. Diagnosis of macroalbuminuria (>300 mg/g creatinine).

  9. 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.

  10. History of malignancy except for completely resected squamous or basal cell carcinoma of the skin.

  11. History of a thromboembolic event (TE), known hypercoagulable state, or condition requiring long-term anticoagulation.

    a. 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.

  12. Known heparin allergy.

  13. Receiving treatment for a medical condition requiring chronic use of systemic steroids, except for physiologic replacement for example in Addison disease.

  14. 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.

  15. Invasive aspergillus, histoplasmosis or coccidioidomycosis infection within one year prior to Screening.

  16. Negative screen for Epstein-Barr Virus (EBV) by immunoglobulin G (IgG) determination.

  17. Current treatment with any immunosuppressive regimen, and treatment with biologic immune modulating agents, Janus kinase (JAK) inhibitors, sphingosine-1-phosphate (S1P) receptor agonists, azathioprine, Mercaptopurine (6- MP), or systemic corticosteroids in the previous 5 years.

  18. 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.

  19. 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.

  20. History of substance abuse within the past 6 months.

  21. Allergy to the Boost drink necessary for MMTT

  22. 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%.

  23. History of significant gastrointestinal disease such as symptomatic cholecystolithiasis; acute or chronic pancreatitis; symptomatic peptic ulcer disease; severe unremitting diarrhea, vomiting or other disorders potentially interfering with the ability to absorb oral medications.

  24. Significant hyperlipidemia despite medical therapy defined as fasting low-density lipoprotein (LDL) cholesterol >130 mg/dL and/ or triglycerides >200 mg/dL.

  25. History of any conditions that can interfere in the assessment of HbA1c due to increased red blood cell turnover or requirement for regular blood transfusions such as sickle cell disease (HbSS, hematopoietic blood stem cell (HbSC), HbS/beta thalassemia); Beta thalassemia major; Alpha Thalassemia (HbH) disease, Hemoglobin H-Constant Spring.

  26. History of any other acute or chronic medical condition or pre-planned medical/surgical procedure that, in the opinion of the Principal Investigator, would compromise the safety of participants or the integrity of study results; non- compliance with recommended diabetes care in the preceding 12 months.

  27. 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.

  28. Any coagulopathy or medical condition requiring long-term anticoagulant therapy (e.g., warfarin) after islet cell transplantation (low-dose aspirin treatment is allowed) or participants with an international normalized ratio (INR) >1.5. The use of Plavix is allowed only when portal vein access is obtained using a mini-laparotomy procedure at the time of islet cell transplant.

  29. History of factor V deficiency.

  30. Administration of live attenuated vaccine(s) within 2 months of Screening.

  31. Any previous treatment with Tegoprubart (AT-1501) or any other anti-CD40L therapy

  32. Baseline Panel-reactive Antibody (PRA) over 20%

  33. Patients with COVID-19 positive PCR tests at the time of Thymoglulin infusion.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Non randomisé
  • Modèle interventionnel: Affectation à un seul groupe
  • Masquage: Aucun (étiquette ouverte)

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Délai
Nombre de participants insulino-indépendants après la première et la dernière greffe
Délai: Jour 75 et jour 365
Jour 75 et jour 365
Nombre de participants avec une hémoglobine glycosylée (HbA1c) <7,0 %
Délai: au jour 365
au jour 365
Nombre de participants sans événements hypoglycémiques graves (SHE) après la première et la dernière greffe
Délai: Jour 28 au jour 365
Jour 28 au jour 365
Nombre de participants présentant un échec de greffe après la greffe finale.
Délai: Jour 365
Jour 365
Number of Participants with glycosylated hemoglobin (HbA1c) <6.5%
Délai: Day 28 through to Day 365
Day 28 through to Day 365
Number of Participants free from SHEs post-first and final transplant.
Délai: Day 28 through to Day 365
Day 28 through to Day 365

Autres mesures de résultats

Mesure des résultats
Délai
Modification de la labilité glycémique après la greffe finale de cellules d'îlots et des années après l'arrêt de l'AT-1501
Délai: Jours 75 et 365, 1-3 ans
Jours 75 et 365, 1-3 ans
Modification du taux d'excrétion d'albumine (AER) après la première et la dernière greffe.
Délai: Jour 365
Jour 365
Modification du débit de filtration glomérulaire estimé (DFGe) après la première et la dernière greffe.
Délai: Jour 365
Jour 365
Changement du pourcentage de nouvelle macroalbuminurie après la première et la dernière greffe.
Délai: Jour 365
Jour 365
Number of Participants who are insulin-independent post- first and final transplant
Délai: 2-3 years
2-3 years
Number of Participants with glycosylated hemoglobin (HbA1c) <7.0%
Délai: at 2 and 3-year follow-up
at 2 and 3-year follow-up
Number of Participants with free of serious hypoglycemic events (SHEs) post-first and final transplant
Délai: Day 28 to 2-3 year follow up
Day 28 to 2-3 year follow up
Number of Participants with HbA1c ≤6.5%
Délai: at 2 and 3-year follow-up.
at 2 and 3-year follow-up.
Number of Participants with free of serious hypoglycemic events (SHEs) post-first and final transplant
Délai: Day 28 to 2-3 years
Day 28 to 2-3 years
Number of Participants with free of serious hypoglycemic events (SHEs) post-first and final transplant
Délai: Day 28 to 2 and 3-year follow-up
Day 28 to 2 and 3-year follow-up
Proportion of participants with graft failure at 2-year and 3-year follow-up post final transplant.
Délai: at 2-year and 3-year follow-up.
at 2-year and 3-year follow-up.

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Chercheur principal: Piotr Witkowski, MD PhD, University of Chicago

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

4 mars 2024

Achèvement primaire (Estimé)

1 mars 2029

Achèvement de l'étude (Estimé)

1 mars 2029

Dates d'inscription aux études

Première soumission

16 février 2024

Première soumission répondant aux critères de contrôle qualité

8 mars 2024

Première publication (Réel)

12 mars 2024

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

22 septembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

17 septembre 2026

Dernière vérification

1 septembre 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Oui

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

S'abonner