Hi TT,
I think this post is a bit disingenuous.
I would encourage you to speak to Management prior to making statements on their behalf. If you had done this you would know that they never expected to replicate the Australian results. Those results were outstanding and surprised even Management. The difficulties in getting a consensus diagnosis in the US is well known and the tightened protocols were effective in delivering results which demonstrate ResappDx is more accurate than a physician in more than 2/3rds of cases (URTI, LRTI and Asthma) with access to the full suite of diagnostics tools. Obviously these tools will not be available to them through a telehealth consult.
The proposition for Resapp remains the same with the company significantly advanced. CE lodgement this year based on the Australian results is highly likely to deliver approval for all respiratory illnesses in Europe. The application for FDA should also be lodged this year with the argument to be made by the company that the app provides a valuable tool to assists doctors in making an diagnosis. This argument is hard to fault when you consider at the moment a diagnosis for URTI, LRTI and Asthma via telehealth is either based solely on listening or cannot be made at all.
I have not even touched on the sleep apnea results or WASH program.
To me the most recent results have shaken out ill-informed investors who were hoping for a single golden goose moment. Unfortunately in the real world amazing companies are built on the back of years of hard work and not a single moment or FOMO.
Everyone is free to make their own investment decisions however I would encourage you to honestly assess the position of company rather than retrospectively justify your decision to sell.
Cheers.
Ann: ResApp Receives Notice of Allowance for Core Patent in Japan, page-46
Currently unlisted. Proposed listing date: 4 SEPTEMBER 2024 #
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