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)
2018年6月7日 更新者: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
調査の概要
詳細な説明
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 .
研究の種類
介入
段階
- フェーズ 4
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究場所
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Madrid、スペイン、28031
- Hospital Infanta Leonor
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Madrid、スペイン、28007
- Hospital Univ. Gregorio Marañon
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Madrid、スペイン、28041
- Hospita 12 de octubre
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Madrid、スペイン、28046
- Hospital Univ. La Paz
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Madri
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Madrid、Madri、スペイン、28046
- Hospital Univ. La Paz
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参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
- 子
- 大人
- 高齢者
健康ボランティアの受け入れ
いいえ
受講資格のある性別
全て
説明
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.
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:Single arm
16 weeks treatment with elbasvir/grazoprevir plus sofosbuvir and ribavirina
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16 weeks treatment
他の名前:
16 weeks treatment
16 weeks treatment
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
時間枠 |
|---|---|
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The rate of patients achieved SVR12
時間枠:Week 12 post treatment
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Week 12 post treatment
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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The proportion of subjects infected with HCV genotype 1a with reference VARs NS5A / NS3 who achieved RVS12.
時間枠: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.
時間枠: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.
時間枠: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.
時間枠: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
時間枠: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
時間枠: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
時間枠: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.
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
|
協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
スポンサー
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (予想される)
2017年7月1日
一次修了 (予想される)
2017年12月1日
研究の完了 (予想される)
2018年2月1日
試験登録日
最初に提出
2017年3月16日
QC基準を満たした最初の提出物
2017年4月6日
最初の投稿 (実際)
2017年4月7日
学習記録の更新
投稿された最後の更新 (実際)
2018年6月8日
QC基準を満たした最後の更新が送信されました
2018年6月7日
最終確認日
2018年6月1日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- GESIDA 9516
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
いいえ
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
いいえ
米国FDA規制機器製品の研究
いいえ
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。
HCVの臨床試験
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Ascletis Pharmaceuticals Co., Ltd.完了
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Ain Shams University完了
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Valme University HospitalBoehringer Ingelheimわからない
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Johns Hopkins UniversityNational Institute of Allergy and Infectious Diseases (NIAID)募集
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National Institutes of Health Clinical Center (CC)Bristol-Myers Squibb; National Institute of Allergy and Infectious Diseases (NIAID)完了
elbasvir/grazoprevirの臨床試験
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ANRS, Emerging Infectious Diseases完了
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University of Illinois at ChicagoMerck Sharp & Dohme LLC完了
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Fundacion Clinic per a la Recerca Biomédica引きこもった
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M.D. Anderson Cancer CenterNational Cancer Institute (NCI)完了ステージ IIIB 肝細胞がん AJCC v7 | IIIC 期の肝細胞がん AJCC v7 | BCLC ステージ B の肝細胞がん | BCLC ステージ C の肝細胞がん | C型肝炎感染症 | ステージ IV の肝細胞がん AJCC v7 | ステージ III 肝細胞がん AJCC v7 | ステージ IIIA 肝細胞がん AJCC v7 | ステージ IVA 肝細胞がん AJCC v7 | ステージ IVB 肝細胞がん AJCC v7 | 難治性肝癌アメリカ