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临床试验/JPRN-UMIN000012937
JPRN-UMIN000012937招募中未知

Efficacy and safety of Simeprevir/PEG alpha-IFN-2a/RBV therapy for patients with chronic hepatitis C after resection of hepatocellular carcinoma - Simeprevir/PEG alpha-IFN-2a/RBV therapy for patients with chronic hepatitisC after resection of HCC

Kansai Medical University0 个研究点目标入组 100 人开始时间: 2014年3月1日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 80years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1.Concomitant herbal medication of Sho-saiko-to. 2.History of interstitial pneumonia 3.Autoimmune hepatitis 4.Allegic to vaccine or biological preperations. 5.Uncontrolled cardiopathy. 6.Hemoglobinopathy. 7.Chronic renal failure or renal dysfunction with creatinine clearance <=50mL/min. 8.Severe depression or psychosomatic disorders. 9.Patients with moderate liver diseases.(Child-Pugh grade BorC) 10.Patient with a history of photosensitivity 11.Women of childbearing potential and pregnancy, lactating women. 12.Drug allegy against interferon or nucleoside analog. 13.Patients receiving rifampicin, rifabutin, phenytoin, carbamazepine, phenobarbital, systemic administration of dexamethasone, azole antifungal drug, clarithromycin, erythromycin, diltiazem, verapamil hydrochloride, cobicistat included drugs,HIV Protease inhibitor, modafinil, nonnucleoside reverse transcriptase inhibitor(except for rilpivirine hydrochloride), bosentan hydrate, St John's Wort included foods, cyclosporine, flecainide, propafenone. 14.Other conditions considered inappropriate by attending physician

研究者

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