Here are my questions for the webinar: 1.How ma
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1.How many man hours to finish the HIV BLA submission and when will it be submitted again?
2.What was the reason the FDA gave for not supporting the 4 dose regimen originally?
3.Why was Dr. Hayden allowed to be on the DSMB committee if there could be a conflict of interest. Who signed off on the members of this committee and was it known at the time there could be a conflict?
4.What trial in progress is the nearest in getting results, either interim or complete and when approximately will that result be announced?
When is the 1st P.O. expected from any country?