Analysis of hepatitis C viral kinetics during administration of two nucleotide analogues: sofosbuvir (GS―7977) and GS―0938

• Published in: Antiviral therapy 2014-01, Vol.19 (2), p.211-220
• Main Authors: GUEDJ, Jeremie, PANG, Phillip S, DENNING, Jill, RODRIGUEZ-TORRES, Maribel, LAWITZ, Eric, SYMONDS, William, PERELSON, Alan S
• Format: Article
• Language: English
• Subjects: Adult; Antibiotics. Antiinfectious agents. Antiparasitic agents; Antiviral agents; Antiviral Agents - therapeutic use; Biological and medical sciences; Cyclic P-Oxides - therapeutic use; Double-Blind Method; Female; Genotype; Hepacivirus - drug effects; Hepacivirus - genetics; Hepatitis C - drug therapy; Hepatitis C - virology; Hepatitis C virus; Human viral diseases; Humans; Infectious diseases; Male; Medical sciences; Middle Aged; Nucleosides - therapeutic use; Pharmacology. Drug treatments; RNA, Viral; Sofosbuvir; Uridine Monophosphate - analogs & derivatives; Uridine Monophosphate - therapeutic use; Viral diseases; Viral hepatitis; Viral Load; Young Adult
• ISSN: 1359-6535; 2040-2058
• DOI: 10.3851/IMP2733

Sofosbuvir (GS-7977) and GS-0938 are nucleotide analogue HCV polymerase inhibitors, with sofosbuvir being a pyrimidine and GS-0938 being a purine. Mathematical modelling has provided important insights for characterizing HCV RNA decline and for estimating the in vivo effectiveness of single direct-acting antiviral agents (DAAs); however it has not been used to characterize viral kinetics with combination DAA therapy. We evaluated the antiviral activity of sofosbuvir and GS-0938 given alone and in combination for 14 days in 32 HCV genotype 1 treatment-naive patients (P2938-0212; NUCLEAR study). Viral load declined rapidly in a biphasic manner in all subjects and could be well fitted by assuming that both drugs had a similar and additive level of effectiveness in reducing viral production equal to 99.96%, on average. The model predicted that this level of effectiveness was not reached until 0.6 and 2 days for GS-0938 and sofosbuvir, respectively, and likely represents the time needed to accumulate intracellular triphosphates. Subsequently, both drugs led to a rapid second phase of viral decline with a mean rate of 0.35 d(-1). No effect of IL28B-polymorphism was found on viral kinetic parameters. Both sofosbuvir and GS-0938 are highly effective at blocking viral production from HCV-infected cells. Both drugs led to a rapid and consistent second phase viral decline and exhibited no breakthroughs or other signs of resistance. From a kinetics perspective, because both drugs were of the same class there was little benefit in combining them, suggesting that future DAA combinations should consider utilizing drugs with different modes of action.