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Breakthrough - T1DM and Chronic Kidney Disease

14. Mai 2026 aktualisiert von: University of Chicago

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).

Studienübersicht

Detaillierte Beschreibung

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.

Studientyp

Interventionell

Einschreibung (Geschätzt)

10

Phase

  • Phase 2
  • Phase 1

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studieren Sie die Kontaktsicherung

Studienorte

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Nein

Beschreibung

Participants are eligible for consideration for the study only if all of the following criteria apply at the time of screening Inclusion:

  1. Subjects 18-70 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, 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.
  6. HbA1c level 6.5% to 9.5% inclusive.
  7. Absence of stimulated C-peptide (<0.3 ng/mL) in response to a mixed- meal tolerance test (MMTT).
  8. Chronic kidney disease stage 1, 2 or 3a
  9. 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
  10. 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:

  1. Body mass index (BMI) >30 kg/m2.
  2. Weight ≤40 kg.
  3. Insulin requirement >60units/day or <15 units/day.
  4. Untreated and uncontrolled proliferative diabetic retinopathy.
  5. Blood pressure: systolic blood pressure (SBP) >140 mmHg or diastolic blood pressure (DBP) >90 mmHg.
  6. Chronic kidney disease stage 3b or above.
  7. Diagnosis of macroalbuminuria (ACR>300 mg/g creatinine).
  8. 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.
  9. History of malignancy except for completely resected squamous or basal cell carcinoma of the skin.
  10. History of a thromboembolic event (TE), known hypercoagulable state, or condition requiring long-term anticoagulation:

    1. 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.
    2. Patients on aspirin are allowed.
  11. Receiving treatment for a medical condition requiring chronic use of systemic steroids, except for physiologic replacement for example in Addison disease.
  12. 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.
  13. Invasive aspergillus, histoplasmosis or coccidioidomycosis infection within one year prior to Screening.
  14. Negative screen for Epstein-Barr Virus (EBV) by immunoglobulin G (IgG) determination.
  15. Current treatment with any immunosuppressive regimen, and treatment with biologic immune modulating agents, JAK inhibitors, S1P receptor agonists, azathioprine, 6- MP, or systemic corticosteroids.
  16. Baseline PRA over 40%
  17. Previous organ transplant (except failed pancreas or islet transplant)
  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. 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%.
  22. Significant hyperlipidemia despite medical therapy defined as fasting low-density lipoprotein (LDL) cholesterol >130 mg/dL and/ or triglycerides >200 mg/dL.
  23. 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.
  24. Administration of live attenuated vaccine(s) within 2 months of Screening.
  25. Any previous treatment with Tegoprubart or any other anti-CD40L therapy

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: N / A
  • Interventionsmodell: Einzelgruppenzuweisung
  • Maskierung: Keine (Offenes Etikett)

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Number of participants who are achieved Optimal outcomes according to Igls criteria
Zeitfenster: 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
Zeitfenster: 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

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Number of participants who achieved insulin independence
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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
Zeitfenster: 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.
Zeitfenster: 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

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

29. April 2026

Primärer Abschluss (Geschätzt)

31. Januar 2030

Studienabschluss (Geschätzt)

31. Januar 2030

Studienanmeldedaten

Zuerst eingereicht

12. Januar 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

14. Mai 2026

Zuerst gepostet (Tatsächlich)

18. Mai 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

18. Mai 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

14. Mai 2026

Zuletzt verifiziert

1. Mai 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Plan für individuelle Teilnehmerdaten (IPD)

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UNENTSCHIEDEN

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Ja

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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