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- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT05302271
Estudo de Fase IA da Terapia Gênica AAVrh.10hFXN para a Cardiomiopatia da Ataxia de Friedreich
The purpose of this study is to test the safety and preliminary efficacy of AAVrh.10hFXN to treat the cardiomyopathy associated with Friedreich's ataxia (FA). AAVrh.10hFXN is a serotype rh.10 adeno-associated virus gene transfer vector coding for Frataxin (FXN). The drug is administered intravenously. This is a phase 1, open label, dose escalation study with a total of 25 participants.
Visão geral do estudo
Status
Tipo de estudo
Inscrição (Estimado)
Estágio
- Fase 1
Contactos e Locais
Contato de estudo
- Nome: Maddie Galbraith, BS
- Número de telefone: 646-962-2672
- E-mail: meg4013@med.cornell.edu
Estude backup de contato
- Nome: Niamh Savage, BS
- Número de telefone: 646-962-5527
- E-mail: nis2049@med.cornell.edu
Locais de estudo
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New York
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New York, New York, Estados Unidos, 10021
- Recrutamento
- Weill Cornell Medicine
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Investigador principal:
- Ronald G Crystal, MD
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Contato:
- Maddie Galbraith, BS
- Número de telefone: 646-962-2672
- E-mail: meg4013@med.cornell.edu
-
Contato:
- Niamh Savage, BS
- Número de telefone: 646-962-5527
- E-mail: nis2049@med.cornell.edu
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-
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Descrição
Inclusion Criteria:
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Males and females, age 12 to 50
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Willing and able to provide informed consent
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Definitive diagnosis of FA, based on clinical phenotype and genotype (GAA expansion on both alleles)
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>600 GAA repeats in intron 1 in at least one allele
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FARS and SARA neurologic scores consistent with diagnosis of Friedreich's ataxia
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Left ventricle ejection fraction (EF) measured by cardiac MRI of ≥35% to 75%
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Evidence of FA-related cardiac disease that falls into one of the 2 categories: Early disease (defined by serum high sensitivity troponin above the normal range, without increased LVMI) or Advanced disease (defined as high sensitivity troponin above the normal range and increased LVMI).
- Increased LVMI in adults: In the absence of other factors known to cause left ventricular hypertrophy, cardiac MRI left ventricular mass index >2 standard deviations above the normal range (males >84 gm/m², females >69 gm/m²)
- Increased LVMI in pediatrics: In the absence of other factors known to cause left ventricular hypertrophy, cardiac MRI left ventricular mass index >95ᵗʰ centile based on normal BSA for their age and gender
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Fibrosis ≤10% in the left ventricular wall on late gadolinium enhancement cardiac MRI
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Resting O2 saturation ≥95%
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Serum neutralizing anti-AAVrh.10 titer <1:125
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Hematocrit >30%
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White blood cell levels within normal limits
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Normal prothrombin, partial thromboplastin time
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Normal liver-related serum parameters (ALT, AST, ALP, bilirubin); normal liver ultrasound and serum alpha fetoprotein
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Normal kidney function as assessed by plasma urea and creatinine; estimated GFR >30 mL/min/1.73m²
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No evidence of active infection of any types, including hepatitis virus (A, B or C), human immunodeficiency virus (HIV-1 and HIV-2), or SARS-CoV2
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Fertile individuals should utilize barrier birth control measures to prevent pregnancy for up to 6 months after vector administration
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Individuals not receiving experimental medications or participating in another experimental protocol for at least 12 wk prior to entry to the study (individuals who are/have received approved therapy will be included).
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Capable of undergoing cardiac MRI
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No contraindications to receiving corticosteroid immunosuppression
Exclusion Criteria:
- Individuals receiving corticosteroids or other immunosuppressive medications
- Individuals with uncontrolled diabetes (glycated hemoglobin, HbA1c levels >7%)
- Genotype FA missense mutation on one or both alleles
- Evidence of infection defined by elevated white blood cell count, temperature >38.5̊ C, infiltrate on chest x-ray
- Decompensated heart failure (NY4A class III-IV at time of baseline clinical assessment)
- Hemoglobin <10 g/dl
- Absolute neutrophil count <1500 cells/mm3
- Platelet count <100,000 cells/mm3
- Hemodynamically unstable atrial or ventricular arrhythmias which require medical intervention
- Contraindication to cardiac MRI (e.g., non-MRI compatible pacemaker/defibrillator) or gadolinium (known or suspected hypersensitivity, glomerular filtration rate <30 mL/min/1.73m2)
- Any malignancy during the last five years, except basal cell skin cancer
- Unrelated clinical condition with life expectancy <12 months (prohibiting follow-up)
- Concomitant conditions (other than FA) known to produce left ventricular hypertrophy, including aortic stenosis, systemic hypertension (BP ≥140/90 on noninvasive blood pressure), or genetically mediated hypertrophic cardiomyopathy
- Use of oxygen supplementation
- Risk for thromboembolic disease, including history of thromboembolic disease hospitalization within the last 90 days, recent trauma and/or recent surgical procedure. If the history of thromboembolic disease is not definitive, the subject will be excluded if laboratory testing suggests a risk for thromboembolic disease because of mutations in the protein-S, protein C, antithrombin, factor V Leiden or prothrombin gene
- Any uncontrolled psychiatric disease
- Pregnant or breastfeeding woman
- Prior participation in any gene and/or cell therapy
- Known obstructive coronary artery disease (as documented by clinical history of myocardial infarction, prior coronary revascularization or angina symptoms (Canadian Cardiovascular Society grade ≥2 at time of baseline clinical assessment), or epicardial obstructive coronary artery disease (≥ 50% left main, ≥ 70% of other major coronary arteries)
- Any lung function abnormalities that would affect cardiopulmonary testing
- Any condition, disorder, or abnormal laboratory test findings at screening which, in the judgment of the investigator, would interfere with the individual's ability to comply with all study requirements, or would require the administration of treatment during the study that could potentially affect the interpretation of the study data, or would place the individual at an unacceptable risk by his/her participation in the study
- If prior infection with SARS-CoV2, any related residual cardiac or pulmonary abnormalities
- Alcoholism or drug addiction (see reference 71 for alcoholism, reference 72 for drug addiction)
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: Não randomizado
- Modelo Intervencional: Atribuição sequencial
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: First Dose Cohort
AAVrh.10hFXN will be administered intravenously. |
AAVrh.10hFXN will be administered intravenously. All participants will remain immunosuppression therapy with prednisone for a total of 14 weeks. |
|
Experimental: Second Dose Cohort
AAVrh.10hFXN will be administered intravenously. |
AAVrh.10hFXN will be administered intravenously. All participants will remain immunosuppression therapy with prednisone for a total of 14 weeks. |
|
Experimental: Third Dose Cohort
AAVrh.10hFXN will be administered intravenously. |
AAVrh.10hFXN will be administered intravenously. All participants will remain immunosuppression therapy with prednisone for a total of 14 weeks. |
|
Experimental: Maximum Tolerated Dose Cohort
AAVrh.10hFXN will be administered intravenously. |
AAVrh.10hFXN will be administered intravenously. All participants will remain immunosuppression therapy with prednisone for a total of 14 weeks. |
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Safety of AAVrh.10hFXN
Prazo: 5 Years
|
To determine the safety of AAVrh.10hFXN, as measured by the number of subjects with any treatment-related adverse events for 5 years. |
5 Years
|
Outras medidas de resultado
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Change in cardiopulmonary exercise testing
Prazo: 5 Years
|
To determine changes in parameters of cardiopulmonary testing (measured by the change in VO2max), from screening (pre-treatment) to up to 5 years post administration. |
5 Years
|
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Change in cardiac-relevant parameters in cardiac-magnetic resonance scans
Prazo: 5 Years
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To determine if there are changes in parameters of cardiac imaging (including Left Ventricular mass, Left Ventricular stroke volume, Global longitudinal strain and wall thickness), from screening (pre-treatment) to up to 5 years post administration. |
5 Years
|
|
Change in cardiac-relevant parameters in echocardiograms
Prazo: 5 Years
|
To determine if there are changes in parameters of echocardiograms (including left ventricle mass, Wall thickness and Left ventricle ejection fraction), from screening (pre-treatment) to up to 5 years post administration. |
5 Years
|
|
Change in arrhythmias with 24-hour monitoring.
Prazo: 5 Years
|
To determine if there are changes in heart arrhythmias, from screening (pre-treatment) to up to 5 years post administration. This will be measure by holter monitoring. |
5 Years
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Ronald G Crystal, MD, Weill Medical College of Cornell University
Publicações e links úteis
Publicações Gerais
- De BP, Cram S, Lee H, Rosenberg JB, Sondhi D, Crystal RG, Kaminsky SM. Assessment of Residual Full-Length SV40 Large T Antigen in Clinical-Grade Adeno-Associated Virus Vectors Produced in 293T Cells. Hum Gene Ther. 2023 Aug;34(15-16):697-704. doi: 10.1089/hum.2023.032.
- Crystal RG, Weinsaft JW, Kaminsky SM, Caragiulo A, Savage N, Patel A, Gavrilova RH, Perlman SL, Galbraith M, Kahlon U, Krishnan U, Kaner RJ, Sanders A, Vo M, Sarva H, Yoo A, Sondhi D, De BP, Mezey JG, Aubert G, Khan A, Selvan N, Bhalla N, Adler E, Zesiewicz T. AAVrh.10hFXN Gene Therapy for the Cardiomyopathy of Friedreich Ataxia: A Nonrandomized Clinical Trial. JAMA Cardiol. 2026 Aug 1;11(8):709-718. doi: 10.1001/jamacardio.2026.1699.
- Hendrickx N, Mentre F, Hamdan A, Karlsson MO, Hooker AC, Traschutz A, Gagnon C, Schule R, Synofzik M, Comets E; ARCA Study Group, EVIDENCE-RND consortium. Comparing randomized trial designs to estimate treatment effect in rare diseases with longitudinal models: a simulation study showcased by Autosomal Recessive Cerebellar Ataxias using the SARA score. BMC Med Res Methodol. 2025 Jul 30;25(1):179. doi: 10.1186/s12874-025-02626-x.
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Real)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
- Manifestações Neurológicas
- Doenças Cerebrais
- Doenças do Sistema Nervoso Central
- Doenças do Sistema Nervoso
- Doenças cardiovasculares
- Condições Patológicas, Anatômicas
- Doenças cardíacas
- Doenças Genéticas, Congênitas
- Doenças Metabólicas
- Doenças Neurodegenerativas
- Distúrbios Heredodegenerativos, Sistema Nervoso
- Doenças da Medula Espinhal
- Discinesias
- Doenças Mitocondriais
- Doenças Cerebelares
- Degenerações espinocerebelares
- Hipertrofia
- Doenças e Anormalidades Congênitas, Hereditárias e Neonatais
- Condições Patológicas, Sinais e Sintomas
- Doenças Nutricionais e Metabólicas
- Sinais e sintomas
- Cardiomiopatias
- Ataxia
- Friedreich Ataxia
- Cardiomegalia
- Compostos policíclicos
- Pregada
- Pregnas
- Esteróides
- Compostos de anel fundido
- PregadaDiols
- Prednisona
Outros números de identificação do estudo
- 20-01021274
- R61HL151355 (Concessão/Contrato do NIH dos EUA)
Plano para dados de participantes individuais (IPD)
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