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辉瑞公司停止开发丙型肝炎药物 已有5人参与
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辉瑞制药有限公司(Pfizer Inc., PFE, 简称：辉瑞公司)已停止丙型肝炎药物的试验开发，退出了行业内为引入新一代丙型肝炎治疗药而进行的激烈竞争。 该公司发言人Victoria Davis称，公司在进行战略评估后决定停止Filibuvir的开发。她表示，这一决定与安全问题无关。 该药在停止开发前处于中期临床试验阶段 |
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丙型肝炎药物竞争好激烈 
6楼2013-03-13 16:05:12
迷你生物学
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小木虫: 金币+0.5, 给个红包，谢谢回帖
痴夷子皮: 金币+1, 谢谢交流。 2013-03-13 08:39:37
小木虫: 金币+0.5, 给个红包，谢谢回帖
痴夷子皮: 金币+1, 谢谢交流。 2013-03-13 08:39:37
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Combination of filibuvir and peginterferon alfa-2a/ribavirin evaluated in HCV patients -------------------------------------------------------------------------------- Filibuvir (PF-00868554; Pfizer) has previously been evaluated as monotherapy in patients with hepatitis C (HCV), and whether the activity seen in that study could be enhanced by combination with peginterferon alfa-2a and ribavirin has now been assessed in a randomized, placebo-controlled trial. Patients with genotype 1 HCV (N = 35) were treated with filibuvir 200, 300 or 500 mg b.i.d. or placebo plus peginterferon alfa-2a 180 mcg/week and ribavirin 1000/1200 mg/day for 4 weeks, with the peginterferon/ribavirin treatment continuing for a further 44 weeks. During the 4-week filibuvir treatment period, the combination therapy was well tolerated, with headache, fatigue, insomnia and nausea the most common adverse events. Adverse events did not appear to be related to filibuvir dose. One serious adverse event related to treatment, elevated creatinine, was seen in the filibuvir 300 mg group. Mean reductions in HCV RNA at day 28 were -2.10, -4.46, -4.67 and -3.62 log10 IU/mL for the placebo and filibuvir 200, 300 and 500 mg groups, respectively. In these groups, 0, 60, 75 and 63% of patients achieved undetectable HCV RNA by week 4 (Jacobson, I. et al. 44th Annu Meet Eur Assoc Study Liver (EASL) (April 22-26, Copenhagen) 2009, Abst). |
2楼2013-03-12 08:26:10
cpujacs
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4楼2013-03-12 12:50:44
fw8505
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5楼2013-03-12 14:42:46