- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07744919
Severe Hepatitis Intervention With Emapalumab for Liver Disease (SHIELD)
A Phase 2 Study of Emapalumab for Prevention of Liver Failure in Pediatric Indeterminate Severe Hepatitis Associated With T-Cell Activation: Severe Hepatitis Intervention With Emapalumab for Liver Disease
The goal of this study is to see whether a medicine called emapalumab, a monoclonal antibody, is safe and works well for patients aged 1 year and older who have indeterminate severe hepatitis with T-cell activation and have not responded well to steroids or still need them.
This study has a Screening Cohort and an Intervention Cohort.
The Screening Cohort will enroll patients with severe hepatitis of all etiologies to observe and collect research samples. Patients enrolled on the Screening Cohort will be asked to participate on the Intervention Cohort if they develop steroid-refractory/ dependent indeterminate severe hepatitis (iSH-T). Additionally, patients may bypass the Screening Cohort and enroll directly in the Intervention Cohort if they already meet its eligibility criteria. Patients in the Intervention Cohort will be treated with emapalumab.
Descripción general del estudio
Descripción detallada
This clinical protocol evaluates the use of emapalumab, an anti-IFN-γ monoclonal antibody, in children aged ≥1 year with steroid-refractory or steroid-dependent indeterminate severe hepatitis with T cell activation (iSH-T). This study aims to establish a safe and effective treatment pathway for a previously steroid-refractory/dependent subjects with iSH-T.
Pediatric severe acute hepatitis is a rare but serious disorder that can rapidly progress to liver failure. Previously healthy children who develop severe acute hepatitis can unpredictably progress to pediatric acute liver failure (PALF) over the course of days to weeks. Importantly, as many as 30-50% of all PALF cases have no specific causal etiology for their liver failure and are termed indeterminate PALF (iPALF) and are at the highest risk for liver transplantation. Work from the PALF study group investigators has identified that iPALF is a leading indication for liver transplantation in children. Additional investigation indicates that iPALF patients have significant T cell activation and CD8+ T cell infiltration of their hepatic tissue. There are reports using immunosuppression in iPALF and PALF with favorable results and it is also the subject of a current multicenter trial in children (NCT04862221).
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 2
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Shanmuganathan Chandrakasan, MD
- Número de teléfono: 404-727-8877
- Correo electrónico: Shanmuganathan.Chandrakasan@emory.edu
Copia de seguridad de contactos de estudio
- Nombre: Maria Frazer
- Número de teléfono: 4047856162
- Correo electrónico: maria.frazer@choa.org
Ubicaciones de estudio
-
-
Georgia
-
Atlanta, Georgia, Estados Unidos, 30322
- Arthur M. Blank Children's Healthcare of Atlanta
-
Contacto:
- Shanmuganathan Chandrakasan, MD
- Número de teléfono: 404-727-8877
- Correo electrónico: Shanmuganathan.Chandrakasan@emory.edu
-
Contacto:
- Kate Silvis
- Correo electrónico: Katherine.Silvis@choa.org
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Niño
- Adulto
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria (Screening Cohort):
- Age: Participants must be ≥ 1 year of age at the time of screening.
- Evidence of Severe Hepatic Injury of all etiology (not just iSH/ iSH-T): Serum alanine aminotransferase (ALT) ≥ 1000 U/L documented within 7 days prior to enrollment.
Exclusion Criteria (Screening Cohort):
- Any condition impairing informed consent/assent or protocol compliance
Inclusion Criteria (Intervention Cohort; patients who meet Intervention Cohort eligibility can bypass Screening Cohort enrollment):
- Steroid-refractory, steroid-dependent, or relapse of hepatitis after stopping steroids and have an Indeterminate etiology of hepatitis based on standard of care, age appropriate evaluation
- Age: ≥ 1 year
- ALT ≥ 1000 U/L prior to initiation of any immune modulatory therapy
Evidence of T-cell activation at initial diagnosis, as indicated by one of the following:
- sIL2R > 2× upper limit of normal (ULN)
- CXCL9 > 5× ULN
- CD8+ T-cell infiltration in the liver
- INR < 2.0 without evidence of hepatic encephalopathy
Exclusion Criteria (Intervention Cohort; patients who meet Intervention Cohort eligibility can bypass Screening Cohort enrollment):
- Patients with known Liver failure (defined as INR >2 on two consecutive occasions without hepatic encephalopathy (HE), or INR ≥1.5 with evidence of HE)
- Evidence of chronic liver disease or parenchymal nodularity as demonstrated on imaging (US, CT, or MRI)
- Evidence of hepatic encephalopathy
- Severe acquired aplastic anemia at presentation
Organ dysfunction assessment defined below:
- Renal dysfunction: eGFR < 30 mL/min/1.73m² or
- Mechanical Ventilation
- Persistent systemic infection despite appropriate antimicrobial therapy
- Active infection with Hepatitis A, B, C, HIV, or herpes simplex virus
- Active mycobacteria (typical and atypical), Histoplasma Capsulatum, Herpes zoster infections.
- Patients with positive respiratory viral infection, including adenovirus, rhinovirus/enterovirus, SARS-CoV-2, influenza, and respiratory syncytial virus, only if they also have declining respiratory function needing positive pressure support. Suspected primary hemophagocytic lymphohistiocytosis based on patients with a history of consanguinity and/or central nervous system dysfunction or other clinical manifestations that is exaggerated compared to the degree of liver dysfunction (as judged by the site investigator and study team)
- Diagnosis of Autoimmune Hepatitis, Wilson Disease, inborn error of metabolism, acute drug or toxin-induced liver injury, or ischemic liver injury
- History of severe hypersensitivity or allergy to any component of this study regimen
- History of confirmed malignancy
- History of recreational drug use within the past 4 weeks, excluding cannabinoids
- Therapy with an immunosuppressive agent or an experimental drug within the past 6 weeks
- Pregnant, planning to become pregnant during study window, or breastfeeding at time of study entry
- Patients of reproductive potential are not eligible unless they have agreed to use an effective contraceptive method (e.g. hormonal contraceptives, intrauterine device, or double-barrier method) for the duration of their study participation. Patients must maintain adequate contraception for at least 4 weeks after their last dose of emapalumab.
- Live-virus vaccination within 4 weeks of study entry or anticipated need for a live or live attenuated vaccine within 4 weeks after the last dose of emapalumab
- Peceived Bacillus Calmette-Guerin vaccine within 12 weeks prior to screening
- Patient or parent/guardian unable to give informed consent or unable to comply with the treatment protocol
- Prisoners will be excluded
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Intervention Cohort
Participants on the Intervention Cohort will receive a combination of immunomodulatory regimen using emapalumab and methylprednisolone (or prednisone equivalent), aimed at controlling severe immune-mediated hepatitis and preventing progression to liver failure. Participants will be monitored closely for clinical improvement, laboratory normalization, and adverse events throughout the 56-day treatment period, with continued follow-up through Day 180 to assess long-term outcomes, including relapse, liver failure, survival, and safety. |
Participants on the Intervention Cohort will receive a combination of immunomodulatory regimen using emapalumab and methylprednisolone (or prednisone equivalent), aimed at controlling severe immune-mediated hepatitis and preventing progression to liver failure.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Incidence of Liver Failure
Periodo de tiempo: 30, 90, and 180 days after the start of emapalumab
|
INR >2 on two consecutive occasions without hepatic encephalopathy (HE), or INR ≥1.5 with evidence of HE
|
30, 90, and 180 days after the start of emapalumab
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Complete Response (CR)
Periodo de tiempo: throughout study participation/ up to 180 days
|
A complete response (CR) is defined by normalization or near-normalization of liver injury markers and hepatic function.
Patients achieving CR will demonstrate an ALT < 2.5X ULN together with an INR ≤ 1.2.
|
throughout study participation/ up to 180 days
|
|
Cytokine and Chemokine Profiling
Periodo de tiempo: through study participation/ up to 180 days
|
The cytokine milieu including interferon-γ, interferon-stimulated gene products, TNF-α, IL-6, IL-18, CXCL9, and others will be quantified to define the inflammatory environment at baseline and during treatment.
|
through study participation/ up to 180 days
|
|
Emapalumab Immunologic Effects
Periodo de tiempo: through study completion/ up to 180 days
|
Change in circulating activated CD8+ T cells from the initiation of emapalumab to Days 7, 14, 30, 60, 90, and 180 of study
|
through study completion/ up to 180 days
|
|
Incidence and Severity of Adverse Events
Periodo de tiempo: from first emapalumab dose through study completion, up to 180 days
|
Incidence of all adverse events of all grades as defined by CTCAE version 5.0
|
from first emapalumab dose through study completion, up to 180 days
|
|
Population Summary Measure
Periodo de tiempo: throughout study participation/ up to 180 days
|
The population summary measure will be the Complete Response rate, which will be estimated as the number of participants with Complete Response divided by the total number of participants in the efficacy sample population.
|
throughout study participation/ up to 180 days
|
|
Time to First Complete Response
Periodo de tiempo: throughout study participation/ up to 180 days
|
Time to first CR will be estimated using time-to-event methods.
Death or liver transplant before CR will be treated as competing risks, and cumulative incidence functions will be used to estimate probabilities.
|
throughout study participation/ up to 180 days
|
|
Partial Response (PR)
Periodo de tiempo: throughout study participation/ up to 180 days
|
This is defined as an ALT decrease 50% from initiation of emapalumab, but ALT >2.5X ULN with INR< 1.2.
|
throughout study participation/ up to 180 days
|
|
Sustained Response Off Therapy (SR)
Periodo de tiempo: throughout study participation/ up to 180 days
|
ALT levels remaining < 2.5X ULN for at least two consecutive months after completion of emapalumab.
|
throughout study participation/ up to 180 days
|
|
Non-Response (NR)
Periodo de tiempo: After 4 doses of emapalumab/ about 2 weeks after start of therapy
|
Patients are considered non-responders if clinically relevant worsening with progression to liver failure.
|
After 4 doses of emapalumab/ about 2 weeks after start of therapy
|
|
Proportion of Patients with Overall Response (CR or PR)
Periodo de tiempo: from first dose of emapalumab to week 8 of therapy
|
The proportion of patients achieving overall response (OR, defined as CR or PR) will be reported at Week 8 with exact confidence intervals.
Missing values will be treated as non-response
|
from first dose of emapalumab to week 8 of therapy
|
|
Time to First Overall Response (OR)
Periodo de tiempo: throughout study participation/ up to 180 days
|
Time to first OR will be analyzed using cumulative incidence methods, with death or liver transplant treated as competing risks.
|
throughout study participation/ up to 180 days
|
|
Sustained CR Off Therapy at Day 180
Periodo de tiempo: 180 days on study therapy
|
The proportion of patients achieving a sustained CR off therapy (SROT) at Day 180 will be summarized with exact confidence intervals.
Patients without Day 180 data or therapy information will be considered non-SROT.
|
180 days on study therapy
|
|
Overall Survival with Native Liver
Periodo de tiempo: days 30, 60, 90, and 180
|
Survival with native liver will be estimated using Kaplan-Meier methods.
Survival probabilities and 95% confidence intervals will be presented at each landmark time point.
|
days 30, 60, 90, and 180
|
|
Proportion of Patients Receiving Liver Transplantation:
Periodo de tiempo: days 30, 90, and 180
|
Cumulative incidence of transplant will be calculated at Days 30, 90, and 180, with death as a competing risk.
|
days 30, 90, and 180
|
|
Change in Systemic Inflammatory Markers
Periodo de tiempo: throughout study participation/ up to 180 days
|
Longitudinal changes in sIL2R, and CXCL9 will be evaluated using mixed-effects models for repeated measures.
|
throughout study participation/ up to 180 days
|
|
Change in Circulating Activated CD8+ T Cells
Periodo de tiempo: throughout study participation/ up to 180 days
|
Changes in activated CD8+ T cells over time will be analyzed similarly with mixed-effects models, supplemented by graphical summaries.
|
throughout study participation/ up to 180 days
|
|
Corticosteroid Exposure and Time to Discontinuation
Periodo de tiempo: throughout study participation/ up to 180 days
|
Cumulative corticosteroid exposure (prednisone equivalents) will be summarized descriptively.
Time to discontinuation will be estimated using Kaplan-Meier methods, with competing-risk analyses considering death or transplant.
|
throughout study participation/ up to 180 days
|
|
Incidence of Hepatitis Relapses
Periodo de tiempo: After initial improvement during weaning or cessation of therapy, up to Day 180
|
Defined as ALT re-elevation with concurrent sIL2R and CXCL9 rise.
Time-to-relapse will be summarized with cumulative incidence functions.
|
After initial improvement during weaning or cessation of therapy, up to Day 180
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
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
Otros números de identificación del estudio
- SHIELD (Jacobs Institute)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Descripción del plan IPD
Study participant research data, which is for purposes of statistical analysis and scientific reporting, will be stored. This will not include the participant's contact or identifying information. Rather, individual participants and their research data will be identified by a unique study identification number. The study data entry and study management systems used by clinical sites and research staff will be secured and password protected.
Neither data nor specimens will be shared across participating sites. Deidentified data that supports the findings of this study will be made available by the Principal Investigator, upon reasonable request.
At the end of the study, all records will continue to be kept in a secure location for as long a period as dictated by local IRB and Institutional regulations. All study databases will be de-identified and archived.
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. .