from the vertex web site:
http://investors.vrtx.com/releasedetail.cfm?ReleaseID=580154
"The approval of INCIVEK was based on data from three Phase 3 studies, which showed that people who received INCIVEK combination treatment achieved significantly higher rates of sustained viral response (SVR, or viral cure) compared to those who received pegylated-interferon and ribavirin alone, regardless of their prior treatment experience:
People new to treatment:
79 percent vs. 46 percent
People who were treated previously but did not achieve a viral cure:
-- Relapsers:
86 percent vs. 22 percent
-- Partial responders:
59 percent vs. 15 percent
-- Null responders:
32 percent vs. 5 percent"
"Prior Relapsers: Defined as people whose hepatitis C virus was undetectable after a full course of previous treatment, but whose virus became detectable during the follow-up period;
Prior Partial Responders: Defined as people who achieved at least a 2 log10 reduction in hepatitis C virus at week 12, but whose hepatitis C virus never became undetectable by week 24 of a prior course of therapy; and
Prior Null Responders: Defined as people who achieved a less than 2 log10 reduction in hepatitis C virus at week 12 of a prior course of therapy."
without referencing relapsers around 60% nonresponders around 40% theres also null responders partial responders and breakthrough
then what is the response for repeaters.like my mom took peg theapy before.
boceprevir is in pharmacies now telaprevir should be by the end of the month they both have the same mechanism of action ( protease inhibitors ) and are comparable in efficacy
mimi that 70% is for first timers only
I have read that the company "Vertex" will be giving FDA's decision of approval status is expected by May 23, 2011. I hear that this med in combination with the pegylated interferon and ribavirin could boost the sustained response rate above 70%..