- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving 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 oppdatert av: 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
Studieoversikt
Status
Tilbaketrukket
Forhold
Intervensjon / Behandling
Detaljert 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 .
Studietype
Intervensjonell
Fase
- Fase 4
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
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Madrid, Spania, 28031
- Hospital Infanta Leonor
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Madrid, Spania, 28007
- Hospital Univ. Gregorio Marañon
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Madrid, Spania, 28041
- Hospita 12 de octubre
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Madrid, Spania, 28046
- Hospital Univ. La Paz
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Madri
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Madrid, Madri, Spania, 28046
- Hospital Univ. La Paz
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Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Barn
- Voksen
- Eldre voksen
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
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
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: N/A
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
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Eksperimentell: Single arm
16 weeks treatment with elbasvir/grazoprevir plus sofosbuvir and ribavirina
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16 weeks treatment
Andre navn:
16 weeks treatment
16 weeks treatment
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
The rate of patients achieved SVR12
Tidsramme: Week 12 post treatment
|
Week 12 post treatment
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
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
|
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
|
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
|
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
|
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
Tidsramme: 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
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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
|
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
|
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
|
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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Forventet)
1. juli 2017
Primær fullføring (Forventet)
1. desember 2017
Studiet fullført (Forventet)
1. februar 2018
Datoer for studieregistrering
Først innsendt
16. mars 2017
Først innsendt som oppfylte QC-kriteriene
6. april 2017
Først lagt ut (Faktiske)
7. april 2017
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
8. juni 2018
Siste oppdatering sendt inn som oppfylte QC-kriteriene
7. juni 2018
Sist bekreftet
1. juni 2018
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
- Sykdommer i fordøyelsessystemet
- RNA-virusinfeksjoner
- Virussykdommer
- Infeksjoner
- Blodbårne infeksjoner
- Smittsomme sykdommer
- Leversykdommer
- Flaviviridae-infeksjoner
- Hepatitt, viral, menneskelig
- Hepatitt, kronisk
- Hepatitt
- Hepatitt C
- Hepatitt C, kronisk
- Molekylære mekanismer for farmakologisk virkning
- Anti-infeksjonsmidler
- Antivirale midler
- Antimetabolitter
- Sofosbuvir
- Ribavirin
- Grazoprevir
- Elbasvir-grazoprevir medikamentkombinasjon
Andre studie-ID-numre
- GESIDA 9516
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
Nei
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .
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