You haven't read the paper, haven't even tried to find the statements/announcements/presentations when they discussed the proposed MoA - where does that leave your statement about that potency assay infringement?
When do you think a MoA and susbequent pote cy assay should be developed? AFTER one failed P3 trial? Or after two? What were Rose's infamous words AFTER applying for a BLA the first time?
Our MC is A$60 million. It wouldn't be that if we weren't still a mile away from possible approval don't you think? Just another statement to try end this conversation and save face.
Let me ask you - do you think at A$60 million MC it requires approval to go to say a A$100 or A$200 million MC? If not, what do you think would be main catalysts to move the CYP SP?
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