the data from the European trial is also required for the TGA submission, specifically the LOD/exposure days. Getting those patients at 1-2 day exposure then 3-5 day exposure etc.
TGA is going by WHO guidelines so we need to collect a lot of data, not just sensitivity and specificity.
i suspect the euro trial is in final stages of choice of clinic and how they will achieve the LLOD of the early stage of infection prior to symptoms.
this will also help our commons list registry. Two birds with one stone.
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