Speculation on my part, could it be that the reaso
Post# of 15624
I speculated about this on the other site, and I certainly don't know. Does anyone know if our FDA must completely agree to the protocol of a trial before it can be put into the database, even if the trial is not being run in the U.S.
It's my belief that Phase 1 and 2's can be run elsewhere, and if data supports it, a Phase 3 can be run in part in the U.S. that can result in approval here.
Gary