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诺华制药丙肝治疗药阿拉泊韦Ⅱ期临床数据发布
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《中国医药导刊》 2011年第11期1926-1926,共1页
据"中国医药报"2011年11月16日报道,诺华制药近日发布报告称,那些未经治疗的丙型肝炎病毒(基因型2和3)的患者,通过无干扰素病毒清除的Ⅱ期试验(阿拉泊韦,即DEB025作为单一药物治疗或同利巴韦林共同治疗),表现出良好的效果。DEB02... 据"中国医药报"2011年11月16日报道,诺华制药近日发布报告称,那些未经治疗的丙型肝炎病毒(基因型2和3)的患者,通过无干扰素病毒清除的Ⅱ期试验(阿拉泊韦,即DEB025作为单一药物治疗或同利巴韦林共同治疗),表现出良好的效果。DEB025属于一类新的名为亲环蛋白抑制剂的药物,因为其有很高的阻隔性。 展开更多
关键词 Ⅱ期试验 治疗 临床数据 病毒 单一治疗 蛋白抑制剂
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经治失败的丙肝患者应用Telaprevir再治疗的效果和耐药特点:一项REALIZE临床试验结果
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作者 马世武 《肝脏》 2013年第6期427-427,共1页
在Ⅲ期REALIZE临床研究中,曾经应用长效干扰素/N巴韦林(PEG/RBV)联合治疗失败(包括53%的复发、19%的部分应答和28%的不应答)的662例基因1型的慢性丙型肝炎病毒感染者,随机分成三组:第一组在应用48周长效干扰素a-2a/利巴韦... 在Ⅲ期REALIZE临床研究中,曾经应用长效干扰素/N巴韦林(PEG/RBV)联合治疗失败(包括53%的复发、19%的部分应答和28%的不应答)的662例基因1型的慢性丙型肝炎病毒感染者,随机分成三组:第一组在应用48周长效干扰素a-2a/利巴韦林之初即联合Telaprevir12周(T12/PR48, 展开更多
关键词 临床试验 特点 应用 患者 长效干扰素a-2a 治疗 慢性 病毒感染者
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Optimizing hepatitis C virus treatment through pharmacist interventions: Identification and management of drug-drug interactions 被引量:5
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作者 Jacob A Langness Matthew Nguyen +2 位作者 Amanda Wieland Gregory T Everson Jennifer J Kiser 《World Journal of Gastroenterology》 SCIE CAS 2017年第9期1618-1626,共9页
To quantify drug-drug-interactions (DDIs) encountered in patients prescribed hepatitis C virus (HCV) treatment, the interventions made, and the time spent in this process.METHODSAs standard of care, a clinical pharmac... To quantify drug-drug-interactions (DDIs) encountered in patients prescribed hepatitis C virus (HCV) treatment, the interventions made, and the time spent in this process.METHODSAs standard of care, a clinical pharmacist screened for DDIs in patients prescribed direct acting antiviral (DAA) HCV treatment between November 2013 and July 2015 at the University of Colorado Hepatology Clinic. HCV regimens prescribed included ledipasvir/sofosbuvir (LDV/SOF), paritaprevir/ritonavir/ombitasvir/dasabuvir (OBV/PTV/r + DSV), simeprevir/sofosbuvir (SIM/SOF), and sofosbuvir/ribavirin (SOF/RBV). This retrospective analysis reviewed the work completed by the clinical pharmacist in order to measure the aims identified for the study. The number and type of DDIs identified were summarized with descriptive statistics.RESULTSSix hundred and sixty four patients (83.4% Caucasian, 57% male, average 56.7 years old) were identified; 369 for LDV/SOF, 48 for OBV/PTV/r + DSV, 114 for SIM/SOF, and 133 for SOF/RBV. Fifty-one point five per cent of patients were cirrhotic. Overall, 5217 medications were reviewed (7.86 medications per patient) and 781 interactions identified (1.18 interactions per patient). The number of interactions were fewest for SOF/RBV (0.17 interactions per patient) and highest for OBV/PTV/r + DSV (2.48 interactions per patient). LDV/SOF and SIM/SOF had similar number of interactions (1.28 and 1.48 interactions per patient, respectively). Gastric acid modifiers and vitamin/herbal supplements commonly caused interactions with LDV/SOF. Hypertensive agents, analgesics, and psychiatric medications frequently caused interactions with OBV/PTV/r + DSV and SIM/SOF. To manage these interactions, the pharmacists most often recommended discontinuing the medication (28.9%), increasing monitoring for toxicities (24.1%), or separating administration times (18.2%). The pharmacist chart review for each patient usually took approximately 30 min, with additional time for more complex patients.CONCLUSIONDDIs are common with HCV medications and management can require medication adjustments and increased monitoring. An interdisciplinary team including a clinical pharmacist can optimize patient care. 展开更多
关键词 Clinical pharmacist Drug-drug interaction Hepatitis C virus treatment
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