I'd really like to read the protocols of the FDA m

I'd really like to read the protocols of the FDA meetings at some point.

Sometimes I am wondering whether a bit more persistance would have produced a different outcome: would the FDA seriously have denied a path for approval with over 80% efficacy with 350mg in an unmet medical need population, if CYDY had insisted on submitting an application for 350mg only at that time with a plan to collect more data post-approval, e.g. collecting safety data fo 525 and 700mg to support future sBLAs could via a pivotal mono trial)? (If they immediately said yes and amen to everything the FDA proposed that would be something else).