"Following receipt of such requests, the Company has supplied Brilacidin to relevant hospitals for individual patient use, with the FDA granting the treating physician permission for the emergency administration of Brilacidin."
Did they mean to say treating physicians? Or did the applications "all" come from one Doctor?
I believe it would be Against HIPPA rules. Cannot release name of hospital since then it would be narrowing down which patients might have requested it and or receive it. Also would be not what the FDA wants to see as a possible “PUMP” and also would create an enormous amount of phone calls to those named hospitals requesting info on the patients.
My sister in Florida caught the Delta last month. At day three while in the hospital a nurse came into my sister’s room with papers. The nurse asked my sister if she wanted to participate in an emergency use drug therapy. My sister was told the name of the drug, and the protocol was all in the paperwork. The catch was, she would have to pay for the drug out of pocket. When my sister turned it down the nurse said that she would too because it was EXPENSIVE!
My sister was never told the exact amount she would have to pay, but it’s interesting to know that compassionate use may come with a price tag to the patient…