Those analyses from various internet boards (I do
Post# of 148238
The RTF letter from FDA was received approx. in July 2020. Why took it almost 15 months for Cytodyn to switch the CRO and sue the hell out of AMAREX? For what were they waiting, a wonder?
The RTF letter is so annihilating (AMAREX looks like a bloody amateur) that it would have been only one consequence back then. Give them a short timeline to fix all this blunders and if not done correctly get the data, switch the CRO and sue the hell out of AMAREX. Or was our contract with AMAREX written by amateurs too?