- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica 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 giugno 2018 aggiornato da: 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
Panoramica dello studio
Stato
Ritirato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
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 di studio
Interventistico
Fase
- Fase 4
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Luoghi di studio
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-
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Madrid, Spagna, 28031
- Hospital Infanta Leonor
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Madrid, Spagna, 28007
- Hospital Univ. Gregorio Marañon
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Madrid, Spagna, 28041
- Hospita 12 de octubre
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Madrid, Spagna, 28046
- Hospital Univ. La Paz
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Madri
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Madrid, Madri, Spagna, 28046
- Hospital Univ. La Paz
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Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
- Bambino
- Adulto
- Adulto più anziano
Accetta volontari sani
No
Sessi ammissibili allo studio
Tutto
Descrizione
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.
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: Single arm
16 weeks treatment with elbasvir/grazoprevir plus sofosbuvir and ribavirina
|
16 weeks treatment
Altri nomi:
16 weeks treatment
16 weeks treatment
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Lasso di tempo |
|---|---|
|
The rate of patients achieved SVR12
Lasso di tempo: Week 12 post treatment
|
Week 12 post treatment
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
The proportion of subjects infected with HCV genotype 1a with reference VARs NS5A / NS3 who achieved RVS12.
Lasso di tempo: 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.
Lasso di tempo: 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.
Lasso di tempo: Week 12 post treatment
|
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.
Lasso di tempo: Week 24 post treatment
|
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
Lasso di tempo: Week 16
|
the occurrence of resistance in patients who did not reach SVR12 after 16 weeks of re-treatment
|
Week 16
|
|
The occurrence of resistance variants (VARs) viral to NS5A or elbasvir, to NS3 or grazoprevir, and to NS5B or SOF in HIV patients included
Lasso di tempo: Week 12 post treatment
|
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
|
|
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
Lasso di tempo: 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.
Lasso di tempo: Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
|
Adverse events
|
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
Lasso di tempo: Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
|
Adverse events
|
Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
|
|
The proportion of subjects with an adverse experience related to medication
Lasso di tempo: Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
|
Adverse events
|
Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
|
|
The proportion of subjects with a severe adverse experience
Lasso di tempo: Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
|
Adverse events
|
Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
|
|
The proportion of subjects with a serious adverse experience related to medication
Lasso di tempo: Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
|
Adverse events
|
Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
|
|
The proportion of subjects with an adverse experience leading to disruption
Lasso di tempo: Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
|
Adverse events
|
Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
|
Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Sponsor
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio (Anticipato)
1 luglio 2017
Completamento primario (Anticipato)
1 dicembre 2017
Completamento dello studio (Anticipato)
1 febbraio 2018
Date di iscrizione allo studio
Primo inviato
16 marzo 2017
Primo inviato che soddisfa i criteri di controllo qualità
6 aprile 2017
Primo Inserito (Effettivo)
7 aprile 2017
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
8 giugno 2018
Ultimo aggiornamento inviato che soddisfa i criteri QC
7 giugno 2018
Ultimo verificato
1 giugno 2018
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
- Malattie dell'apparato digerente
- Infezioni da virus a RNA
- Malattie virali
- Infezioni
- Infezioni a trasmissione ematica
- Malattie trasmissibili
- Malattie del fegato
- Flaviviridae Infezioni
- Epatite, virale, umana
- Epatite cronica
- Epatite
- Epatite C
- Epatite C, cronica
- Meccanismi molecolari dell'azione farmacologica
- Agenti antinfettivi
- Agenti antivirali
- Antimetaboliti
- Sofosbuvir
- Ribavirina
- Grazoprevir
- Combinazione di farmaci Elbasvir-grazoprevir
Altri numeri di identificazione dello studio
- GESIDA 9516
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
No
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
No
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
No
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
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