Sofosbuvir plus velpatasvir plus voxilaprevir for the treatment of hepatitis C infection

被引:9
|
作者
Cory, Theodore J. [1 ]
Mu, Ying [1 ]
Gong, Yuqing [2 ]
Kodidela, Sunitha [2 ]
Kumar, Santosh [2 ]
机构
[1] Univ Tennessee, Ctr Hlth Sci, Coll Pharm, Dept Clin Pharm & Translat Sci, Memphis, TN 38163 USA
[2] Univ Tennessee, Ctr Hlth Sci, Coll Pharm, Dept Pharmaceut Sci, Memphis, TN 38163 USA
基金
美国国家卫生研究院;
关键词
Hepatitis C; NS3 protease inhibitor; NS5A inhibitor; NS5B polymerase inhibitor; sofosbuvir; velpatasvir; voxilaprevir; VIRUS-INFECTION; OPEN-LABEL; PHASE-2; TRIAL; GENOTYPE; 1-4; INHIBITOR; PSI-7977; GS-9857; THERAPY; REPLICATION; COMBINATION;
D O I
10.1080/14656566.2018.1459567
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Hepatitis C is a disease with a significant global impact. Over the last several years, the treatment of the disease has been revolutionized. Therapy has transformed over the last several years with the approval of second generation direct acting antivirals, and currently utilized medications for the treatment of hepatitis C are significantly more efficacious with better safety profiles than previously approved treatments. Treatment for individuals who have failed therapy on direct acting antivirals has, until recently, been complex and difficult to treat, but the approval of sofosbuvir/velpatasvir/voxilaprevir represents a new therapeutic option for these individuals.Areas covered: Sofosbuvir/velpatasvir/voxilaprevir is a recently approved therapeutic combination for the treatment of hepatitis C. This article reviews the studies leading to the approval of the combination, and its efficacy and safety profile.Expert opinion: Sofosbuvir/velpatasvir/voxilaprevir fills one of the previously unfilled niches for the treatment of hepatitis C, that of the treatment of individuals who have failed therapy with resistant virus. With the filling of this niche, there appears to be a general slowing of the development of new therapeutics. Although understandable, in the long term, there are considerable risks associated with the decreased development of new drugs to treat hepatitis C.
引用
收藏
页码:749 / 757
页数:9
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