CureOrBust wrote:
even if lesions and symptoms may come and go on the individual, I think they would rely on the statistical outcomes.
Statisical outcomes in trials can be manipulated to "prove" a point. That's how Copaxone eventually got approved after first being rejected by the FDA for statistical insignificance. In reference to your previous question on lesions, the companies always show that there are fewer lesions for those who take the drug vs those who don't. But while being a nice stat, it doesn't translate into the drug having a good efficacy.
We often hear that certain drugs reduce the number of exacerbations by about 33% over placebo. So if a patient had 2 attacks a year, they now have 1.3 attacks! Is that really helpful in view of the side effects and cost of the medication? I guess it depends on how one looks at it.
In the case of Tysabri, Biogen told us that the reduction in risk of attack was 67% over placebo, whatever "reduction in risk" means.
The companies who conduct these trials spend a ton of money on them and they need to ensure statistical significance to get approval. The temptation to manipulate can be very high when the reward in drug sales is so high.
Harry