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Re: polaco3us post# 82301

Thursday, 09/27/2018 1:31:19 PM

Thursday, September 27, 2018 1:31:19 PM

Post# of 108192
The FDA errs on the side of caution when promising approval if the SPA is used and the endpoints are met. So they require a large patient number, long study times, randomization, blinding, etc. That is my understanding. The flip side is, there is no risk of doing a study that the FDA later says was not sufficient to permit approval.
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