It seemed like everybody, other nations, FDA etc., when responding to our m/m Top Line report, the all wanted to wait for Phase III s/s Interim report. But, nobody is allowed to see the interim analysis, unless the were waiting for the extremes recommendations, such as "halt and FDA approval coming ASAP" or "halt due to poor efficacy (no way)" or how would other nations respond if it was "continue with Phase III s/c tirals"????
So what would they be happy with????
Or might even other nations be in unspoken subtle ways, be influenced by power players and/or big pharma???