Agree that the Covid trial results could TRUMP everything and be a pathway for approval for Ryoncil. My concern is is it possible that the FDA have thought to themselves ok are we going to approve this treatment or not and then based a decision on how these current Covid trials are going and seen the interim results of 90 patients and then gone , results are not that great we wont have to worry about that making us look like fools?. I am a total believer in MSB so after today i am just thinking of all angles. Basically would the FDA have access from the DSMB of current interim results?
Also some great posts here and hopefully once this meeting happens all will be resolved?
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