A Study of RO5024048 in Combination With Ritonavir-Boosted Danoprevir and Pegasys/Copegus in Patients With Chronic Hepatitis C Genotype 1 Who Have Failed Prior HCV Protease Inhibitor Treatment
试验速览
- 阶段
- 2 期
- 状态
- 撤回
- 主要终点
- Sustained virologic response (defined as unquantifiable serum HCV RNA) 12 weeks after treatment (SVR-12)
研究概览
简要总结
This randomized, double blind, phase II study will evaluate the efficacy and safety of two doses of RO5024048 in combination with ritonavir-boosted danoprevir and Pegasys (peginterferon alpha-2a) and Copegus (ribavirin) in patients who failed a prior protease inhibitor containing regimen with or without pegylated interferon. Patients will be randomized to receive either a 2-week lead-in of RO5024048 (1500 mg or 1000 mg orally twice daily) in combination with Pegasys (180 mcg subcutaneously weekly) and Copegus (1000 mg or 1200 mg orally daily) followed by 24 weeks of therapy with RO5024048 in combination with danoprevir (100 mg orally twice daily) plus ritonavir (100 mg orally twice daily) and Pegasys and Copegus (QUAD therapy), or 24 weeks of therapy with RO5024048 in combination with danoprevir plus ritonavir and Pegasys and Copegus (QUAD therapy). Anticipated time on study treatment is 24 or 26 weeks, with a treatment-free follow-up of 24 weeks.
研究设计
- 研究类型
- Interventional
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Adult patients, >/= 18 years of age
- •Hepatitis C genotype 1 infection
- •Serum HCV quantifiable by Roche COBAS TaqMan HCV Test v2.0
- •Liver biopsy (within 24 months) or Fibroscan (within 12 months) before first administration of study drug consistent with chronic hepatitis C and demonstrating absence of liver cirrhosis
- •Documented failed prior treatment with protease inhibitor (evidenced by viral breakthrough or partial response while on treatment or relapse after treatment), including documentation on treatment with other direct-acting antiviral agents and other HCV antiviral treatment
- •Patients must have discontinued prior HCV treatment at least 24 weeks prior to first dose of study drug in this trial
排除标准
- •Infection with any HCV genotype other than genotype 1
- •Evidence of any variants associated with protease inhibitor resistance at screening
- •Body mass index (BMI) <18 or >/=36 kg/m2
- •Positive for hepatitis A or hepatitis B infection
- •Use of any systemic antiviral therapy with perceived activity against HCV </=1 month prior to first dose of study drug
- •History or evidence of a medical condition associated with chronic liver disease other than chronic hepatitis C
- •Pregnant or breastfeeding women
- •Males with female partners who are pregnant
- •History of immunologically mediated disease; patients with rheumatoid arthritis requiring only intermittent non-steroidal anti-inflammatory medications or with celiac disease will be allowed
- •History or evidence of decompensated liver disease
- •History or evidence of renal disease; patients with history of nephrolithiasis will be allowed
- •Uncontrolled Type 1 or 2 diabetes
- •History or evidence of chronic pulmonary disease associated with functional limitation
- •History of severe cardiac disease History of any neoplastic disease within the last 5 years, except for localized or in situ carcinoma of the skin (e.g. basal or squamous cell carcinoma)
- •Evidence of excessive alcohol, drug or substance abuse (excluding marijuana use) within 1 year of the first dose of study drug
研究组 & 干预措施
1000 mg 26 weeks
干预措施: danoprevir (Drug)
1500 mg 26 weeks
干预措施: danoprevir (Drug)
1000 mg 24 weeks
干预措施: RO5024048 (Drug)
1000 mg 24 weeks
干预措施: danoprevir (Drug)
1000 mg 24 weeks
干预措施: peginterferon alfa-2a [Pegasys] (Drug)
1000 mg 24 weeks
干预措施: ribavirin [Copegus] (Drug)
1000 mg 26 weeks
干预措施: RO5024048 (Drug)
1000 mg 26 weeks
干预措施: peginterferon alfa-2a [Pegasys] (Drug)
1000 mg 26 weeks
干预措施: ribavirin [Copegus] (Drug)
1000 mg 26 weeks
干预措施: ritonavir (Drug)
1500 mg 24 weeks
干预措施: RO5024048 (Drug)
1500 mg 24 weeks
干预措施: danoprevir (Drug)
1500 mg 24 weeks
干预措施: peginterferon alfa-2a [Pegasys] (Drug)
1500 mg 24 weeks
干预措施: ribavirin [Copegus] (Drug)
1500 mg 24 weeks
干预措施: ritonavir (Drug)
1500 mg 26 weeks
干预措施: RO5024048 (Drug)
1500 mg 26 weeks
干预措施: peginterferon alfa-2a [Pegasys] (Drug)
1500 mg 26 weeks
干预措施: ribavirin [Copegus] (Drug)
1500 mg 26 weeks
干预措施: ritonavir (Drug)
结局指标
主要结局
Sustained virologic response (defined as unquantifiable serum HCV RNA) 12 weeks after treatment (SVR-12)
时间窗: approximately 2 years
次要结局
- Sustained virologic response 4 weeks after treatment (SVR-4)(approximately 2 years)
- Sustained virologic response 24 weeks after treatment (SVR-24)(approximately 2 years)
- Change in serum HCV RNA levels(from baseline to Week 12)
- Safety: Incidence of adverse events(approximately 2 years)
- Virologic response over time(from baseline to 24 weeks after treatment)
- Correlation between trough concentrations of RO4995855 and virologic response(approximately 2 years)
- Incidence of direct-acting antiviral (DAA) resistance, including re-emergence of protease inhibitor resistant virus(approximately 2 years)