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They did a very, very exceptionally clever trial design and were able to get to advocacy in a relatively small number of people in very quick time to get through their phase two. And it surprised everybody, quite honestly, in a positive way, how fast theyre able to do that. It took certainly less than a year. an emergency use authorization is not usually used, and that is where you get through early studies and show its safe and youre given permission to start distributing it more widely.