That makes sense.
However I have a further question that someone may have some suggestions.
I also note that we are doing further safety trials at higher doses just in case the higher doses may be required. Is this SOP or does it maybe signal that there is a question about effecasy at the existing trial dosage?? If it is standard procedure then there is no message to be gained except that congratulations for diligence. If not standard then is there something we will get to know at Q2 results?
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