雷迪帕韦（英语：Ledipasvir，亦作GS-5885）是吉利德科学研发的治疗C型肝炎的药物。在完成了Ⅲ期临床试验后，吉利德于2014年2月10日向美国联邦政府申请报批了固定剂量复方片剂，复方索非布韦雷迪帕韦片，用于第1基因型C型肝炎病毒感染的治疗。

The ledipasvir/sofosbuvir combination is a direct-acting antiviral agent that interferes with HCV replication and can be used to treat patients with genotypes 1a or 1b without PEG-interferon or ribavirin.

Ledipasvir (formerly GS-5885) is a drug for the treatment of hepatitis C that was developed by Gilead Sciences. After completing Phase III clinical trials, on February 10, 2014 Gilead filed for U.S. approval of a ledipasvir/sofosbuvir fixed-dose combination tablet for genotype 1 hepatitis C. The ledipasvir/sofosbuvir combination is a direct-acting antiviral agent that interferes with HCV replication and can be used to treat patients with genotypes 1a or 1b without PEG-interferon or ribavirin.