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Re: hankmanhub post# 292259

Sunday, 06/28/2020 7:32:55 PM

Sunday, June 28, 2020 7:32:55 PM

Post# of 709756
hankmanhub,

here are some recent quotes from iwasadiver:

Wednesday, 05/13/20 12:23:25 PM

The UK is taking over for all new drug approvals from the EMA, right now. DCVax is on the expedited review list with only another 200 or so drugs and it could be as quickly as 4 months.
https://investorshub.advfn.com/boards/read_msg.aspx?message_id=155605945


Thursday, 05/14/20 07:47:29 AM

The EMA has nothing to do with an already existing MHRA authority to approve drugs for use only in the UK. Then NICE, AWMSG (All Wales Medicines Strategy Group), SMC (Scottish Medicines Consortium), DoH (Northern Ireland’s Dept. of Health) assess for cost guidance, etc.
https://investorshub.advfn.com/boards/read_msg.aspx?message_id=155622375


Friday, 05/15/20 08:56:38 PM
I think there will be some sort of news before November about an application to the MHRA and an expected timeline for an answer for approval and NICE recommendations
https://investorshub.advfn.com/boards/read_msg.aspx?message_id=155671633


The past few weeks I contacted the UK government. I was surprised they responded to all my enquiries.(And in such a short time)
I can confirm that the quotes from iwasadiver are true!
Obviously, the data of the DCvax-L trial must be very good to be admitted for this accelerated procedure.
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