A clinical
trial last month showed that a once daily, all-oral drug combination to treat
chronic hepatitis C infection (HCV)--Bristol-Myers Squibb’s daclatasvir (NS5A
replication complex inhibitor) and Gilead’s sofosbuvir (nucleotide NS5B
inhibitor), direct-acting viral agents--was effective in all patients. It
tested that drug combination with and without ribavirin, and excluded
interferon, which is notorious for causing debilitating side effects. Results
of the trial were presented by Mark Sulkowski, MD, professor of medicine at
Johns Hopkins University during the 48th Annual Meeting of the European
Association for the Study of the Liver (International Liver Congress 2013),
April 24-28, 2013, in Amsterdam, The Netherlands.
All 41 study
subjects had genotype 1 chronic HCV. More than 80% had subtype 1a, which is
difficult to treat. They represented HCV patients who did not respond
previously to interferon-based triple therapy using pegylated interferon and ribavirin,
with an approved HCV protease inhibitor, either boceprevir (Victrelis) or telaprevir (Incivek).
Twelve weeks
after the treatment ended, the rates of sustained viral response (SVR) were
100% in the sofosbuvir/daclatasvir arm and 95% in the
sofosbuvir/daclatasvir/ribavirin arm. SVR
indicates that a patient has “cleared” the virus for at least six months after
completing therapy. It is achieved when viral levels drop to nearly
undetectable levels.
Of the 21
patients who completed 24 weeks of follow-up once treatment ended, all had
undetectable virus, or 100% SVR in both arms. Researchers reported that the
drugs were well tolerated and there were few side effects.
“These data
provide proof-of-concept that the combination of two potent direct-acting
antivirals with different viral targets is effective in patients who failed
[pegylated interferon/ribavirin] plus a protease inhibitor,” concluded
Sulkowski. “We can tell our patients who failed triple therapy they now appear
to have a path forward toward a cure.”
Source: AIDSmap.com, April 29, 2013
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