Drug intelligence / Profile preview

PPI-668 + BI 207127 + faldaprevir + ribavirin

Development stage
Phase 2
Lead developer
Presidio Pharmaceuticals
Modality
Small Molecules
Administration
Oral
01

Overview

This combination is an **investigational oral regimen for the treatment of chronic hepatitis C virus (HCV) infection**, composed of four antiviral agents: - **PPI-668**: a potent, pan-genotypic HCV NS5A inhibitor developed by Presidio Pharmaceuticals. - **BI 207127 (deleobuvir)**: a non-nucleoside inhibitor of the HCV polymerase (NS5B), developed by Boehringer Ingelheim, active mainly against genotype 1. - **Faldaprevir (BI 201335)**: an oral, once-daily HCV NS3/4A protease inhibitor from Boehringer Ingelheim. - **Ribavirin**: a broad-spectrum antiviral nucleoside analog, usually combined with other anti-HCV agents. The regimen was studied in Phase 2 trials as a potential **interferon-free, all-oral therapy** for HCV genotype 1 infection, with and without ribavirin, aiming to achieve rapid and sustained virologic responses (SVR) with improved tolerability. Boehringer Ingelheim and Presidio Pharmaceuticals collaborated in these clinical trials focused on patients with genotype 1a HCV infection[1][3][5].

02

Targets

NS3/4A (Hepatitis C virus nonstructural protein 3/4A serine protease)NS5A (Hepatitis C virus nonstructural protein 5A (genotype 1b))NS5B (Hepatitis C virus non-structural protein 5B (NS5B) RNA-dependent RNA polymerase)IMPDH (Inosine-5'-monophosphate dehydrogenase 1)Neuraminidase

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