Belatacept in De Novo Heart Transplantation

Официальное название

Belatacept in De Novo Heart Transplantation - Pilot Study

Обзор

The purpose of this study is to determine if Belatacept is safe to give to adult heart transplant recipients. Belatacept (NULOJIX) is an anti-rejection medication that is available through a prescription from a doctor. In this research study, belatacept is being used in an investigational manner (not for the purpose that it is approved for).

Подробное описание

Long-term outcomes after heart transplant remain suboptimal with renal failure and cardiac allograft vasculopathy contributing to morbidity and mortality. Belatacept is Food and Drug Administration (FDA) approved for use in kidney transplant recipients on the basis of two randomized controlled trials, which demonstrated important renal sparing benefits, a reduction in de novo donor-specific antibodies (DSA), and improved long-term outcomes. In this study, ten (10) primary heart transplant recipients will receive belatacept in addition to mycophenolate mofetil, corticosteroids, and a tacrolimus tapering regimen.

Вмешательства

• Препарат Belatacept
  Belatacept will be given in the following way - 10mg/kg IV day 1, 5, end of weeks 2, 4, 8, 12 then 5mg/kg every 4 weeks.
• Препарат Tacrolimus
  Non-experimental: Tacrolimus will be given in the following way - trough level at month 1, 10-12ng/mL; month 2-3, 6-10ng/mL; month 4-6, 4-6ng/mL; months 7-9 taper off.
• Препарат Mycophenolate Mofetil
  Non-experimental: MMF is part of standard of care after heart transplant and will follow dosing recommendations as per standard clinical practice at 500-1500mg twice a day (BID) (dosed to tolerance and effect).
• Препарат Corticosteroid
  Non-experimental: CS is part of standard of care after heart transplant and will follow dosing recommendations as per standard clinical practice at a dose no less than 5mg/d.

Первичные конечные точки

• Number of Major Graft-Related Adverse Events [Срок оценки: Up to 18 months after transplantation]

Вторичные конечные точки (2)

• Change in Estimated Glomerular Filtration Rate (eGFR) [Срок оценки: Baseline and 18 months]
• Percentage of Individuals with Development of De Novo Donor Specific Antibodies (DSA) [Срок оценки: 18 months]

Критерии участия

Критерии включения

• Male or non-pregnant female, age ≥18 to ≤75 years
• Awaiting a primary heart transplant (listed for heart transplant only)
• Epstein-Barr virus (EBV) IgG seropositive
• Able to take oral medication and willing to adhere to the belatacept infusion regimen
• No desensitization therapy prior to transplant
• Vaccinations should be up to date for hepatitis B, influenza pneumococcal, haemophilus, varicella zoster virus (VZV), measles, mumps and rubella (MMR), and Human Papilloma Virus (HPV) (for participants < 45 years of age) when available
• Female subjects of childbearing potential must have a negative pregnancy test (serum or urine) prior to randomization
• Mechanical support or investigational drug trials where the intervention ends at the time of transplantation are permitted
• Negative virtual crossmatch

Критерии исключения

• Candidates awaiting multiorgan transplant
• Estimated glomerular filtration rate (eGFR) < 45 ml/min/m2
• Candidates with prior organ transplant
• Candidates actively being treated with immunosuppressive therapies
• Candidates who have a history of treatment with cytolytic therapy (e.g. anti-thymocyte globulin)
• Candidates who are intended to be treated with cytolytic therapy in the post-transplant period as induction therapy
• EBV (IgG) seronegative
• Active or prior infection with human immunodeficiency virus (HIV), Hepatitis C (HCV), Hepatitis B (HBV)
• Untreated latent tuberculosis (TB)
• All potential candidates will be screened prior to enrolment for a history of tuberculosis (chest radiograph and tuberculosis-Interferon Gamma Release Assay (TB-IGRA) or tuberculin skin tests (TST)). Potential candidates with latent TB must be treated prior to study enrolment
• Prior history of active tuberculosis
• Prior history of central nervous system infection
• Known active current viral, fungal, mycobacterial, or other infections excluding driveline infections - potential participants from endemic areas will additionally be screened for histoplasmosis, blastomycosis, coccidioidomycosis, and strongyloidiasis
• Vaccination with a live vaccine within the past 30 days
• Malignancy within the last 5 years
• Any previous treatment with alkylating agents or total lymphoid irradiation
• Sensitized heart transplant candidates with panel-reactive antibodies (PRA) >50% or those receiving desensitization treatment
• Prior treatment with belatacept or abatacept
• History of severe allergic anaphylactic reactions to humanized or murine monoclonal antibodies
• Treatment with a disease modifying anti-rheumatic drug (DMARD) or other biologic agent (monoclonal antibody) within the past year
• Treatment with another investigational drug or other intervention at the time of transplant (excluding device or intervention mechanical support or investigational drug trials where the intervention ends at the time of transplant)
• Potential candidates for whom a calcineurin inhibitor other than tacrolimus (Prograf®) is anticipated after transplant. If during the course of the study, a participant is transitioned to another calcineurin inhibitor due to side effects or inability to achieve stable therapeutic trough levels, they may continue in the study at the discretion of the investigator
• Any potential participant who remains on mechanical circulatory support for > 72 hours post-transplant will be excluded from the study
• The need for ongoing high dose vasopressor support > 72 hours post-transplant
• The need or anticipated need for post-transplant dialysis
• Platelet count <75,000/mm (within 24 hours prior to transplant)
• Absolute neutrophil count (ANC) of less than 2000/mm3 within 24 hours prior to transplant
• Any past or current medical problems or findings on history, physical examination, or laboratory testing, not listed above, that in the opinion of the investigator, may pose additional risk to participation, may interfere with the participant's ability to comply with study requirements, or that may impact the quality or interpretation of study results

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение

Не применимо

Модель

Одна группа

Маскирование

Открытое

Основная цель

Профилактика

Центры проведения

США · 2 центра

• NYU Langone Health — New York
• Columbia University — New York

Идентификаторы

NCT: NCT04477629 · 22-01135

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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