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ducruacuteo11

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ducruacuteo11

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Thursday, 12/22/2016 11:45:59 AM

Thursday, December 22, 2016 11:45:59 AM

Post# of 43835
I finally took some time and reread the filings and am even more confused. If the IDMC recommended that the trial be put on hold, why didn't the FDA follow through? They enrolled 926 patients altogether. And if multikine is unsafe, why did the FDA only put on a partial hold and allow them to continue to administer the drug to existing, enrolled patients? If some of you can shed any light into this, I would greatly appreciated.
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