Cytodyn delivered the initial items the FDA wanted then they asked for additional data after that, then asked for clarification, then the last item was an HIV protocol. Except a protocol has nothing to do with a safety hold since it is for a trial that hasn't taken place yet therefore offers no safety data. Whenever I think of that last ask for an HIV protocol before the safety hold is lifted I become irate. It's a good thing I don't work for Cytodyn or I would pointedly ask why the safety hold is being predicted on non-existent data, pissing off the FDA in the process.