- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg 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. juni 2018 opdateret af: 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
Studieoversigt
Status
Trukket tilbage
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
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 .
Undersøgelsestype
Interventionel
Fase
- Fase 4
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Madrid, Spanien, 28031
- Hospital Infanta Leonor
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Madrid, Spanien, 28007
- Hospital Univ. Gregorio Marañon
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Madrid, Spanien, 28041
- Hospita 12 de octubre
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Madrid, Spanien, 28046
- Hospital Univ. La Paz
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Madri
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Madrid, Madri, Spanien, 28046
- Hospital Univ. La Paz
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Barn
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
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.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: Single arm
16 weeks treatment with elbasvir/grazoprevir plus sofosbuvir and ribavirina
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16 weeks treatment
Andre navne:
16 weeks treatment
16 weeks treatment
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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The rate of patients achieved SVR12
Tidsramme: Week 12 post treatment
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Week 12 post treatment
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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The proportion of subjects infected with HCV genotype 1a with reference VARs NS5A / NS3 who achieved RVS12.
Tidsramme: 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.
Tidsramme: 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.
Tidsramme: 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.
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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.
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Forventet)
1. juli 2017
Primær færdiggørelse (Forventet)
1. december 2017
Studieafslutning (Forventet)
1. februar 2018
Datoer for studieregistrering
Først indsendt
16. marts 2017
Først indsendt, der opfyldte QC-kriterier
6. april 2017
Først opslået (Faktiske)
7. april 2017
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
8. juni 2018
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
7. juni 2018
Sidst verificeret
1. juni 2018
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Sygdomme i fordøjelsessystemet
- RNA-virusinfektioner
- Virussygdomme
- Infektioner
- Blodbårne infektioner
- Overførbare sygdomme
- Leversygdomme
- Flaviviridae infektioner
- Hepatitis, viral, menneskelig
- Hepatitis, kronisk
- Hepatitis
- Hepatitis C
- Hepatitis C, kronisk
- Molekylære mekanismer for farmakologisk virkning
- Anti-infektionsmidler
- Antivirale midler
- Antimetabolitter
- Sofosbuvir
- Ribavirin
- Grazoprevir
- Elbasvir-grazoprevir lægemiddelkombination
Andre undersøgelses-id-numre
- GESIDA 9516
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Ingen
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med HCV
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Ascletis Pharmaceuticals Co., Ltd.Afsluttet
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Ain Shams UniversityAfsluttet
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PfizerAfsluttet
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Bristol-Myers SquibbAfsluttetHCV (genotype 1)Forenede Stater, Puerto Rico
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Valme University HospitalBoehringer IngelheimUkendtHCV-infektion. | HCV viral belastning.Spanien
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State University of New York at BuffaloIkke rekrutterer endnu
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Johns Hopkins UniversityNational Institute of Allergy and Infectious Diseases (NIAID)Rekruttering
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CepheidEmory UniversityAfsluttet
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Tibotec Pharmaceuticals, IrelandAfsluttet
Kliniske forsøg med elbasvir/grazoprevir
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Institut de Médecine et d'Epidémiologie Appliquée...Merck Sharp & Dohme LLC; Institut National de la Santé Et de la Recherche...Afsluttet
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National Cheng-Kung University HospitalMerck Sharp & Dohme LLCAfsluttetPotentisering af lægemiddelinteraktionTaiwan
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University Hospital, ToulouseMSD FranceAfsluttetKroniske nyresygdomme | Hepatitis CFrankrig
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Erasmus Medical CenterAfsluttetHepatitis C | Humant immundefektvirus | Akut hepatitis CHolland, Belgien
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San Francisco Veterans Affairs Medical CenterMerck Sharp & Dohme LLCUkendt
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Merck Sharp & Dohme LLCAfsluttet
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King Fahad Medical CityAfsluttetHepatitis C, kroniskSaudi Arabien
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Merck Sharp & Dohme LLCAfsluttet
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University of Maryland, BaltimoreMerck Sharp & Dohme LLC; Cairo UniversityTrukket tilbageHepatitis C-virusinfektion, respons på terapi afEgypten
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Kirby InstituteAfsluttet