A Single-Arm Study to Provide Boceprevir Treatment in Subjects with Chronic Hepatitis C Genotype 1 Deemed Nonresponders tPeginterferon/Ribavirin in Previous Schering-Plough Boceprevir Studies - PROVIDE

Schering-Plough Research Institute, A Division of Schering Corporation0 个研究点目标入组 340 人开始时间: 2009年6月11日最近更新: 2019年6月30日

适应症

试验速览

暂无简介。

•1. Subject must have been assigned to a peginterferon/RBV control arm in a previous SPRI study of boceprevir, must have completed treatment as per protocol, and have been compliant with all study treatment and scheduled procedures within the previous study 2. Subject must have received at least 12 weeks of treatment with peginterferon/RBV and must have discontinued treatment in the previous study due to the futility rule (as defined in the previous protocol), had virologic breakthrough, or relapse 3. Subject must have had detectable HCV-RNA upon completion of the previous study 4. Subject and subject?s partner(s) must each agree to use acceptable methods of contraception for at least 2 weeks prior to starting any study treatment and to continue until at least 6 months after the last doses of study drugs, or longer if dictated by local regulations 5. Subject must be willing to give written informed consent
•Are the trial subjects under 18? no
•Number of subjects for this age range:
•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) yes
•F.1.3.1 Number of subjects for this age range

•1. All subject exclusion criteria from the SPRI clinical study in which the subject participated prior to qualifying for this study will apply in this study, EXCEPT for the following: a. Treatment with ribavirin within 90 days and any interferon-alpha within1 month of the enrollment is not exclusionary in P05514 b. Participation in any other SPRI clinical trial within 30 days of enrollment in this study is not exclusionary c. Use of growth factor at the entry of the study is allowed if it was prescribed in the previous study d. Laboratory criteria of thyroid-stimulating hormone (TSH) do not apply. Laboratory criteria of hemoglobin, neutrophis, and platelets do not apply, unless they met dose reduction/interruption/discontinuation criteria in the previous study e. Subjects who develop moderate depression in the previous study and continue to be stable and well controlled are not excluded 2. Subjects had the opportunity to receive boceprevir 3. Subjects requiring discontinuation, interruption, previous study 4. Subjects requiring discontinuation, interruption,of the assigned starting dose for more than 2 weeks 5. Subjects who experienced a life-threatening SAE investigator or sponsor in the previous study

发起方

Schering-Plough Research Institute, A Division of Schering Corporation