Further to my earlier post re Leslie's interview of 16 April in which she said ... "We also have 2 oncolytic viral therapy studies,CHECKVac and Vaccinia, and they're both at the door of the FDA IMD in order to pursue a clinical trial." ... the reason I say we may expect news on this any day now is the following:
"Once an IND is submitted, the FDA has 30 days to object to the IND or it automatically becomes effective and clinical trials may begin. If the FDA detects a problem, it may place a clinical hold on the IND, prohibiting the start of the clinical studies until the problem is resolved." https://en.wikipedia.org/wiki/Investigational_New_Drug
Who knows how many days prior to the interview of 16 April the oncolytic studies were delivered to the FDA IMD' s door for approval!
IMUGENE CHART. TA only, page-246
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