AVE avecho biotechnology limited

Ann: Licensing Webinar and Presentation, page-83

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    I expect there will also be a urine screen with analysis followed by a clinical interview to establish the protocol around a normalised sleeping environment prior to a 14 to 21 day baseline period being established for each participant. The baseline protocols would i imagine match the dosing period protocols and 'sleep diaries' and 'wearable monitors' would be mandatory ( think these wearables are possibly one of PGs' 'big ticket items' that he enthusiastically mentioned a few times in the webinar from memory as they would collect and collate gathered data in real time)

    all clinical interviewers must be blinded to the treatment protocol as you would expect

    suggestions that the partner may have glimpsed or been privy to some sort of 'result' or ongoing outcome are not correct imo - why place in jeopardy all data outcomes and trial legitimacy in such a way on a global phase 3 trial - pretty sure Sandoz Group AG would have run a mile if such data had become available in any format


    red or black as always

 
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