Cytodyn Inc (CYDY): The FDA wanted the data from the monothe...

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Re: Black-Ops post# 121487

Tuesday, 10/06/2020 10:36:50 AM

Tuesday, October 06, 2020 10:36:50 AM

The FDA wanted the data from the monotherapy trial that was collected between January 2020 and June 2020 (end of trial). We do have someone highly experienced at BLA submission and I think it was said, well known by the FDA, who has been hired to handle the BLA submission for HIV combo therapy. Which will allow Amarex to concentrate on COVID-19 and yes Amarex has quite a few BLA submissions that led to approval.

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