An evaluation of the cyclophilin inhibitor Debio 025 and its potential as a treatment for chronic hepatitis C

作者:Crabbe Raf*; Vuagniaux Gregoire; Dumont Jean Maurice; Nicolas Metral Valerie; Marfurt Judith; Novaroli Laura
来源:Expert Opinion on Investigational Drugs, 2009, 18(2): 211-220.
DOI:10.1517/13543780802651583

摘要

Debio 025 is a cyclophilin (Cyp) inhibitor without calcineurin-binding properties. The drug inhibits viral replication of genotype 1b and 2a replicons in nanomolar concentrations and shows an additive to synergistic antiviral effect with interferon, ribavirin, and specifically targeted antiviral therapy for hepatitis C (STAT-C) drugs. There is no cross-resistance with protease and polymerase inhibitors. In humans, Debio 025 has shown activity against genotypes 1, 2, 3, and 4, and displays an additive antiviral effect with pegylated interferon (peg-IFN)alpha 2a in genotype 1 and 4 patients. The most prominent side effect is reversible hyperbilirubinaemia caused by inhibition of biliary transporters. Debio 025 is a potent anti-HCV drug, with a novel mechanism of action and an efficacy profile that makes it an attractive candidate for combination with current and future HCV treatments.

  • 出版日期2009-2