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Chemical compound From Wikipedia, the free encyclopedia
Faldaprevir was an experimental drug for the treatment of hepatitis C (HCV). It was being developed by Boehringer-Ingelheim and reached Phase III clinical trials in 2011.[1] Boehringer announced in 2014 that it would not pursue approval of the drug any more because of better HCV treatments having become available.[2]
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Other names | BI 201335 |
Routes of administration | By mouth |
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Formula | C40H49BrN6O9S |
Molar mass | 869.83 g·mol−1 |
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Faldaprevir is a hepatitis C virus protease inhibitor.[citation needed]
Faldaprevir was tested in combination regimens with pegylated interferon and ribavirin, and in interferon-free regimens with other direct-acting antiviral agents including deleobuvir.[citation needed]
Data from the SOUND-C2 study, presented at the 2012 AASLD Liver Meeting, showed that a triple combination of faldaprevir, deleobuvir, and ribavirin performed well in HCV genotype 1b patients.[3]
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