跳至主要内容
临床试验/EUCTR2010-020034-26-IT
EUCTR2010-020034-26-IT进行中(未招募)不适用

A multicenter, randomized, open label, parallel-groupphase IIB study on the efficacy and safety of oral regimensof DEB025 alone or in combination with ribavirin versusStandard of Care (peg-IFNa2a plus ribavirin) in treatmentnaïvehepatitis C genotype 2 and 3 patients

OVARTIS FARMA0 个研究点目标入组 400 人开始时间: 2011年12月28日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
OVARTIS FARMA
入组人数
400

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Key inclusion criteria are:
  • Written informed consent prior to any assessment;
  • Males or females aged =18 and = 65 years;
  • BMI between = 18 and = 32 kg/m2;
  • Chronic hepatitis C virus infection;
  • Plasma HCV RNA = 10000 IU/ml; no upper limit;
  • Infection with HCV genotype 2 or 3;
  • HCV treatment naïve;
  • Female patients of child bearing potential must have a negative pregnancy test immediately prior
  • to first administration of study drug.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range: 0
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Key exclusion criteria are:
  • Use of other investigational drugs at the time of enrollment, or within 30 days or 5 half-lives of
  • enrollment, whichever is longer;
  • Any contraindications to peg-IFNa2a and/or RBV treatment;
  • Active or suspected cancer, or a history of malignancy where the risk of recurrence is = 20% within
  • HBsAg positive or HIV positive;
  • Cirrhosis, decompensated liver disease or complicated portal hypertension;
  • Hepatocellular carcinoma;
  • Pregnant, nursing or lactating women or women of child-bearing potential UNLESS they are using
  • two birth control methods;
  • Men whose female partners are pregnant or contemplating pregnancy. Fertile males UNLESS the
  • patient and his partner agree to comply with acceptable contraception;
  • Ongoing or recent use of any other medication (including over the counter medication and herbal
  • products) within 2 weeks before study start or within 5 drug half-lives of that medication (whichever is longer) that are known inhibitors/inducers of cytochrome 450 3A, substrates of cytochrome 450
  • 3A, substrates of P-gp, or substrates/inhibitors of OATPs, MRP2 or BSEP;
  • Any other cause of relevant liver disease other than HCV;
  • History of moderate, severe, or uncontrolled psychiatric disease, especially depression.

研究者

发起方
OVARTIS FARMA

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