“Further analyses of clinical effectiveness are being conducted for those EPP patients who continue treatment and those who received their first treatment after 30 June 2017”
Hmmm....I hope this “Further analyses” of post 30 June data is not needed to finalise the FDA Submission.
Otherwise i’d expect further delays on that of at least 2 - 3 months.
Ann: CLINUVEL hosts European EPP Expert Meeting, page-3
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