- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT03105349
A Clinical Trial of 16 Weeks of Duration to Evaluate Retreatment With Elbasvir/Grazoprevir Plus Sofosbuvir and Ribavirin in Patients With Chronic Hepatitis C Genotypes 1,4 Who Have Failed to Treat With a Regime Based on an Inhibitor of the NS5A (C-RESCUE)
7 de junio de 2018 actualizado por: Fundacion SEIMC-GESIDA
A Phase III, Open Label, Multicentric Clinical Trial of a Single Arm of 16 Weeks of Duration to Evaluate Retreatment With Elbasvir/Grazoprevir Plus Sofosbuvir and Ribavirin in Patients With Chronic Hepatitis C Genotype 1,4 Who Have Failed to Treat With a Regime Based on an Inhibitor of the NS5A
This is a phase 4 clinical trial to treat patients who have failed to treat with regimen based on an inhibitor of the NS5A
Descripción general del estudio
Estado
Retirado
Condiciones
Intervención / Tratamiento
Descripción detallada
The duration of the treatment will be 16 weeks and then will be a security perid with 2 visits (Week 12 post treatment and week 24 post treatment) The study in an open label study with a single arm .
Tipo de estudio
Intervencionista
Fase
- Fase 4
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Ubicaciones de estudio
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Madrid, España, 28031
- Hospital Infanta Leonor
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Madrid, España, 28007
- Hospital Univ. Gregorio Marañon
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Madrid, España, 28041
- Hospita 12 de octubre
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Madrid, España, 28046
- Hospital Univ. La Paz
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Madri
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Madrid, Madri, España, 28046
- Hospital Univ. La Paz
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Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
- Niño
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
No
Géneros elegibles para el estudio
Todos
Descripción
Inclusion Criteria:
- Adults with chronic HCV genotype 1, 4 infection with or without HIV infection aged 18 years or above
- HCV RNA plasma concentration of at least 1000 IU / mL
- Subjects previously treated with NS5A-based regimens for at least 8 weeks.
- Patients with HCV relapse after receiving a complete treatment with NS5A-based AAD regimen for at least 8 weeks and becoming undetectable at the end of treatment. Relapse is defined as a confirmed HCV RNA detectable upon completion of therapy of A5 based on NS5A against HCV.
- Subjects with compensated hepatic cirrhosis (Child A) could be included.
For patients with HIV coinfection:
- Be infected with HIV-1, documented by any rapid HIV test with the corresponding license and confirmed by a Western blot or second antibody test using a method other than the initial rapid HIV and / or I / CIA method or by HIV-1 p24 antigen or viral load of HIV-1 RNA plasma.
- Be on stable HIV antiretroviral therapy (ART) for at least 4 weeks prior to entry into the study using a dual ITN backbone of tenofovir or abacavir and emtricitabine or lamivudine PLUS raltegravir or dolutegravir or rilpivirine (with CD4 + T cell count> 100 cells / mm 3 and undetectable HIV-1 RNA at baseline. Results from prior analysis will be accepted within 24 weeks prior to study entry).
Exclusion Criteria:
- Subjects with hepatitis other than C or steatosis.
- Subjects previously treated less than 8 weeks with regimens based on NS5A.
- Evidence of previous hepatocellular carcinoma although it has criteria of cure
- Subjects with past or current decompensated liver disease; Only decompensated patients who have received a liver transplant and have not decompensated after transplantation will be included.
- Subjects suspected of clinical or genotypic reinfection of HCV.
- Subject with HCV response regrowth while receiving NS5A-based ADA therapy against HCV. Said regrowth is defined as a confirmation of detectable HCV RNA after achieving undetectable HCV RNA during NS5A-based AADs against HCV.
- Recent history of drug or alcohol abuse.
Important comorbidities.
- Pregnant, lactating or non-lactating women Contraceptives, if they are women of childbearing age. Women of childbearing age are defined as those women who have not undergone permanent infertility procedures or who have been amenorrheic for less than 12 months.
- Subjects with a glomerular filtration rate of less than 30 ml / min.
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿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 |
|---|---|
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Experimental: Single arm
16 weeks treatment with elbasvir/grazoprevir plus sofosbuvir and ribavirina
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16 weeks treatment
Otros nombres:
16 weeks treatment
16 weeks treatment
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Periodo de tiempo |
|---|---|
|
The rate of patients achieved SVR12
Periodo de tiempo: Week 12 post treatment
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Week 12 post treatment
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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The proportion of subjects infected with HCV genotype 1a with reference VARs NS5A / NS3 who achieved RVS12.
Periodo de tiempo: Week 12 post treatment
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To analyze the impact of VARs NS5A/NS3 on RVS12
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Week 12 post treatment
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The proportion of subjects infected with HCV genotype 1b with reference VARs NS5A / NS3 who achieved RVS12.
Periodo de tiempo: Week 12 post treatment
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Analyze the impact of VARs NS5A/NS3 on RVS12
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Week 12 post treatment
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The proportion of subjects infected with HCV genotype 4 with reference VARs NS5A /NS3 who achieved RVS12.
Periodo de tiempo: Week 12 post treatment
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Analyze the impact of VARs NS5A/NS3 on RVS12
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Week 12 post treatment
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The proportion of subjects infected with HCV genotypes 1.4 with reference VARs NS5A /NS3 who achieved RVS24.
Periodo de tiempo: Week 24 post treatment
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Analyze the impact of VARs NS5A/NS3 on RVS24
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Week 24 post treatment
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The occurrence of Viral resistance variants (VARs) to NS5A or elbasvir, to NS3 or grazoprevir and to NS5B or SOF in patients who did not reach SVR12 after 16 weeks of re-treatment
Periodo de tiempo: Week 16
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the occurrence of resistance in patients who did not reach SVR12 after 16 weeks of re-treatment
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Week 16
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The occurrence of resistance variants (VARs) viral to NS5A or elbasvir, to NS3 or grazoprevir, and to NS5B or SOF in HIV patients included
Periodo de tiempo: Week 12 post treatment
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The impact of VARs NS5A/NS3 on RVS12 The proportion of subjects developing HIV-1 virological failure (HIV RNA> 200 Copies / mL), confirmed in 2 consecutive tests with at least 2 weeks between them. |
Week 12 post treatment
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The proportion of subjects developing HIV-1 virological failure (HIV RNA> 200 Copies / mL), confirmed in 2 consecutive tests with at least 2 weeks between them
Periodo de tiempo: Week 4, week 8, week 12 and week 16
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the impact of treatment with EL / BRA plus SOFT and ribavirin in HIV-1 subjects
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Week 4, week 8, week 12 and week 16
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The proportion of subjects experiencing adverse events of high laboratory values who report as ECI at any time during the study period.
Periodo de tiempo: Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
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Adverse events
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Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
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The proportion of subjects with at least one adverse experience
Periodo de tiempo: Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
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Adverse events
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Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
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The proportion of subjects with an adverse experience related to medication
Periodo de tiempo: Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
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Adverse events
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Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
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The proportion of subjects with a severe adverse experience
Periodo de tiempo: Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
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Adverse events
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Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
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The proportion of subjects with a serious adverse experience related to medication
Periodo de tiempo: Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
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Adverse events
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Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
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The proportion of subjects with an adverse experience leading to disruption
Periodo de tiempo: Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
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Adverse events
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Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
|
Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio (Anticipado)
1 de julio de 2017
Finalización primaria (Anticipado)
1 de diciembre de 2017
Finalización del estudio (Anticipado)
1 de febrero de 2018
Fechas de registro del estudio
Enviado por primera vez
16 de marzo de 2017
Primero enviado que cumplió con los criterios de control de calidad
6 de abril de 2017
Publicado por primera vez (Actual)
7 de abril de 2017
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
8 de junio de 2018
Última actualización enviada que cumplió con los criterios de control de calidad
7 de junio de 2018
Última verificación
1 de junio de 2018
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
- Enfermedades del Sistema Digestivo
- Infecciones por virus de ARN
- Enfermedades virales
- Infecciones
- Infecciones transmitidas por la sangre
- Enfermedades contagiosas
- Enfermedades del HIGADO
- Infecciones por Flaviviridae
- Hepatitis, Viral, Humana
- Hepatitis Crónica
- Hepatitis
- Hepatitis C
- Hepatitis C Crónica
- Mecanismos moleculares de acción farmacológica
- Agentes antiinfecciosos
- Agentes Antivirales
- Antimetabolitos
- Sofosbuvir
- Ribavirina
- Grazoprevir
- Combinación de fármacos elbasvir-grazoprevir
Otros números de identificación del estudio
- GESIDA 9516
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
No
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
No
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
No
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. .
Ensayos clínicos sobre elbasvir/grazoprevir
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National Cheng-Kung University HospitalMerck Sharp & Dohme LLCTerminadoPotenciación de la interacción farmacológicaTaiwán
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Institut de Médecine et d'Epidémiologie Appliquée...Merck Sharp & Dohme LLC; Institut National de la Santé Et de la Recherche Médicale...TerminadoVIH | Hepatitis C agudaFrancia
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Erasmus Medical CenterTerminadoHepatitis C | Virus de inmunodeficiencia humana | Hepatitis C agudaPaíses Bajos, Bélgica
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University Hospital, ToulouseMSD FranceTerminadoEnfermedades Renales Crónicas | Hepatitis CFrancia
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King Fahad Medical CityTerminadoHepatitis C CrónicaArabia Saudita
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San Francisco Veterans Affairs Medical CenterMerck Sharp & Dohme LLCDesconocido
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University of Maryland, BaltimoreMerck Sharp & Dohme LLC; Cairo UniversityRetiradoInfección por el virus de la hepatitis C, respuesta a la terapia deEgipto
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Merck Sharp & Dohme LLCTerminado
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Oregon Health and Science UniversityTerminadoAbuso de Sustancias, Intravenoso | Hepatitis C | Trastornos por uso de sustanciasEstados Unidos
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Kirby InstituteTerminado