Combination of two antivirals for treating hepatitis C
An antiviral agent and a treatment process technology, applied in the field of combination of two antiviral agents for the treatment of hepatitis C, can solve problems such as incomplete elimination of the virus
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Embodiment 1
[0118] Example 1. Clinical modeling of DAA combination therapy without interferon
[0119] The treatment regimen comprising administration of Compound 1 and Compound 2 used the clinical model described in U.S. Patent Application Publication No. 2013 / 0102526, filed October 19, 2012 and entitled "Methods for Treating HCV," which is incorporated herein by reference in its entirety. to evaluate. These treatment regimens included the administration of Compound 1 and Compound 2, but not the administration of interferon or ribavirin.
[0120] figure 1 Shown are the predicted median SVR percentages and 90% SVR for the 2-DAA regimen consisting of Compound 1 (400 mg once daily) and Compound 2 (120 mg once daily) to treat genotype 1 naïve subjects confidence interval. Different treatment durations were evaluated. The predicted SVR rate for 12-week treatment was approximately 95%. As used in all figures in this application, the vertical bar at the top of each SVR percentage column re...
Embodiment 2
[0126] Example 2. Combination of Compound 1 and Compound 2 in vitro
[0127] Figure 7 It was shown that the combination of Compound 1 and Compound 2 exhibited a significant synergistic effect on HCV inhibition as tested in HCVGT1bCon-1 replicating cells. Results were generated using the Prichard and Shipman model (Prichard et al. Antiviral Research 14:181-205 (1990)).
[0128] Compound 1 inhibits the replication of HCV stable subgenomic replicons containing the NS3 gene from GT1a, 1b, 2a, 3a, 4a or 6a, where EC 50 Values range from 0.85 to 2.8 nM. Notably, compound 1 is potent against replicon containing GT3a protease, in which EC 50 The value is 1.6nM. Compound 1 retained its activity against common GT1a and 1b variants at NS3 amino acid positions 155 and 168 that confer resistance against other HCV protease inhibitors (Pis). Resistant colony selection studies in GT1a and 1b subgenomic replicon cells identified A156T in GT1a and A156V in GT1b as the most common varian...
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