The wording used was actually "anticipated" . Given the 4-5 week delay at the start ("actual") I suspect we're on a similar timeline for last/final patient. From that point we have a short timeframe for final dosage of the final patient before they're in a position to do a preliminary read out. BTW I understand it was quite a demanding clinical process for those involved (twice a week and +1 hour a session). So a big thanks to those on here that put their hand up and endured the trial program.
research reports and media, page-2975
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