- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07705789
The Role of interferOn and Complement in SecondAry thRombotic micrioangiOpathy (ROSARIO)
The Role of interferOn and Complement in SecondAry thRombotic micrioangiOpathy (ROSARIO)
Study rationale: Viral infections, such as CMV, are a risk factor for TA-TMA (transplantation-associated TMA). Viral infections increase interferon (IFN) levels and high IFN levels are associated with thrombotic microangiopathy (TMA). IFNs contribute to TMA pathogenesis through suppression of VEGF transcription. Disruption of the VEGF signalling pathway in the kidney is associated with TMA.
Primary objective: To determine the association between IFN levels and the development of biopsy-proven or clinically diagnosed TA-TMA.
Secondary objective(s): To explore the relationship between complement activation and IFN in patients with TMA.
To explore if high IFN levels are associated with low VEGF-A levels. Endpoint: The study aims to investigate the role of IFN in the pathogenesis of secondary thrombotic microangiopathy (focusing on patients with TA-TMA). It seeks to clarify whether IFN, next to complement dysregulation, is a driver of endothelial damage and TMA in these patients.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Fase
- No aplica
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Sofie A Dhaese, MD, PhD
- Número de teléfono: +320050452200
- Correo electrónico: sofie.dhaese@azsintjan.be
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
Participants eligible for inclusion in this study must meet all of the following criteria:
- Voluntary written informed consent of the participant or their legally authorized representative has been obtained prior to any screening procedures
- At least 18 years of age at the time of signing the Informed Consent Form (ICF)
Specifically for the patients with TMA (G1 and G4):
- Patients after allogeneic or autologous hematopoietic stem cell transplantation (HSCT) OR patients after solid organ transplantation OR patients with DITMA AND
- Tissue diagnosis of TMA (pathological diagnosis) OR
Clinical diagnosis of TMA based on the following criteria, with ≥4 out of 6 features fulfilled within 14 days (15,52,53):
de novo Coombs negative hemolytic anemia OR (in case of HSCT)
- failure to achieve transfusion independence despite neutrophil engraftment
- hemoglobin decline by ≥ 1g/dL
- new onset transfusion dependence
otherwise unexplained de novo thrombocytopenia (< 50 x 109/L) OR a 25% decrease in platelet count OR (in case of HSCT)
- failure to achieve platelet engraftment despite neutrophil engraftment
- higher than expected transfusion needs
- refractory to platelet transfusion *≥50% reduction in platelet count after full platelet engraftment
- lactate dehydrogenase (LDH) above the upper limit of normal
- schistocytes (=>2 / high power field (HPF)
- new onset hypertension OR worsening of existing hypertension requiring additional antihypertensive therapy
- proteinuria > 1g/g creatinine on a random urine protein-to-creatinine ratio Date of TMA diagnosis = first date when ≥4 out of the 6 features are fulfilled.
Specifically for the group of patients without TMA, with infection (G2):
- Patients after allogeneic or autologous hematopoietic stem cell transplantation (HSCT) OR patients after solid organ transplantation AND
- Symptomatic viral infection (evaluated by the treating physician).
Specifically for the group of patients without TMA, without infection (G3):
- Patients after allogeneic or autologous hematopoietic stem cell transplantation (HSCT) OR patients after solid organ transplantation AND
- No symptomatic viral infection (evaluated by the treating physician).
Exclusion Criteria:
Participants eligible for this study must not meet any of the following criteria:
- Participant has a personal or family history of aHUS
- Participant has a history of malignant hypertension
- Participant has a history of active cancer, excluding the haematological cancer for which the patient received the stem cell transplantation (if applicable)
- The participant received prior complement inhibition
- The participant received prior anti-interferon treatment
- If applicable: Female who is pregnant, breast-feeding or intends to become pregnant the following year or is of child-bearing potential and not using an adequate, highly effective contraceptive
- Participation in an interventional study with an investigational medicinal product (IMP) or device
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Otro: Patients with HSCT-TMA or SOT-TMA
blood and urine collection
|
blood sampling at designated time points
urine collection at designated time points
|
|
Otro: Patients after HSCT or SOT with a viral infection, without TMA
blood and urine collection
|
blood sampling at designated time points
urine collection at designated time points
|
|
Otro: Patients after HSCT or SOT without a viral infection, without TMA
blood and urine collection
|
blood sampling at designated time points
urine collection at designated time points
|
|
Otro: Patients with drug-induced TMA (DITMA)
blood and urine collection
|
blood sampling at designated time points
urine collection at designated time points
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Interferon signature
Periodo de tiempo: Time point 1: baseline Time point 2: up to week 52
|
6-gene interferon signature
|
Time point 1: baseline Time point 2: up to week 52
|
|
VEGF-A
Periodo de tiempo: Time point 1: baseline Time point 2: up to week 52
|
VEGF-A level
|
Time point 1: baseline Time point 2: up to week 52
|
|
Complement analysis (serum)
Periodo de tiempo: Time point 1: baseline Time point 2: up to week 52
|
CH50, AP50, C3, C3d, C4 and C5b-9 at timepoint 1 and C5b-9 at time point 2
|
Time point 1: baseline Time point 2: up to week 52
|
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
Palabras clave
Términos MeSH relevantes adicionales
- Citopenia
- Enfermedades hematológicas
- Trastornos de las plaquetas sanguíneas
- Trombocitopenia
- Enfermedades hemic y linfáticas
- Microangiopatías trombóticas
- Técnicas de investigación
- Manejo de muestras
- Técnicas de laboratorio clínico
- Técnicas y procedimientos de diagnóstico
- Diagnóstico
- Puntas
- Procedimientos quirúrgicos, operativo
- Recolección de muestras de sangre
- Colección de muestras de orina
Otros números de identificación del estudio
- ROSARIO
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.
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .