The FDA, the TGA, the EMA will not give a flying rats arse about results in an Indonesia trial, I can assure you.
If Indo was some sort of magical short cut, every biotech in the world would be doing it.
If quick revenue is not the purpose, then there is literally no reason to bother with this trial.
If the goo is so effective, why not go straight to a trial under an IND in the USA (or somewhere sensible?
There is only one reason I can think of and it involves gravy being near a train.
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Ann: Positive Phase II Data from Clinical Trial of R327 Gel, page-48
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