>…on the 20% increase basis, the control group is going to need to be extremely hard to treat and get a number perhaps as low as 32% SVR, and perhaps as high as 37%.<
It looks like it will be 35-36%, but it could be a little lower or perhaps a point higher.
>However you cut it, that would be a very tough control group to treat…<
Yes, your explanation is the correct one: the patient pool in the Boceprevir trial was clearly harder to treat than the patent pool in the PROVE-1 and PROVE-2 studies. That’s why Boceprevir’s 55-56% SVR in the short-duration arms is very impressive.
Let’s talk biotech! “The efficient-market hypothesis may be the foremost piece of B.S. ever promulgated in any area of human knowledge!”