And the issues in that statement were addressed by a revised SAP filed prior to unblinding and approved by the regulators. You dismiss facts to continually quote a risk factor. Risk factors are mean to to state what are the absolutely worst things can happen, so that shareholders have heard absolutely anything that could possibly go wrong. But you know already for a fact that PFS is no longer the primary endpoint, OS is and you know the reason, the placebo arm having almost a 90% crossover, because of perceptions of success by patients and doctors, meant that they were able to use an external control arm, which was approved and discussed in the May and subsequent presentations.
So when you repeatedly post and say these things, knowing what you know and without discussion, you post incomplete information.
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