PAR paradigm biopharmaceuticals limited..

Ann: Appendix 3B, page-6

  1. 4,920 Posts.
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    Well I'm no expert in MCTT (Medical Clinical Trial Timelines) but Im guessing you could minus 3 months from Prep time (trial design, Pre 3 meetings with FDA etc), and at least another 3 months for recruitment and then a full 1 year min for the trial and then 6 months to review results, whats that, a total of say 2 years saving. Thats the whole idea, its such a critically required drug, its safe and there is NOTHING else that can be currently used, its filling an unmet need.
    SO instead of it being 1.5 years (Phase 2) plus 2 years min (Phase 3), we might get away with just 2 years all up before commercialisation. This is also postulated by 51Capital who suggested something like a 2021 release for PPS to combat MPS.

    Long time frames sure, but hey, 2 years is better than 4 plus.

    Do your own research, these are just my opinions.

 
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