RE: Type A meeting24 Nov 2020 15:11
The 10th November 2020 RNS said:
"Following the notification by ImmuPharma, on 27 July 2020, that Avion Pharmaceuticals ("Avion"), ImmuPharma's licensing partner for Lupuzor™ had submitted a Special Protocol Assessment ("SPA") request to the US Food & Drug Administration ("FDA") for the new optimised international Phase 3 study, the FDA has now responded."
It says the submission was made as notified by Imm on 27th July 2020 and "...the FDA has NOW responded." (emphasis added).
Seems clear to me that following the SPA request the response was only just received. The RNS states submission has been accepted and the Type A meeting is to discuss the matters set out in the RNS.