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Re: exwannabe post# 505201

Monday, 08/15/2022 4:33:07 PM

Monday, August 15, 2022 4:33:07 PM

Post# of 823457

I guessed you missed the NYAS (and other) presentations that clearly disagreed with your post,

I guess you really are in need of reading glasses. No better reality check. From the NY Conference:

Secondary Endpoint: OS in recurrent GBM
Placebo arm crossovers* (n=64) vs. External controls (n=640)
*(Placebo arm patients received only SOC (control arms of external studies)
+ placebo until recurrence, then DCVax-L)

At the NY conference, the secondary endpoint for nGBM was not mentioned. Get a pair of reading glasses, +5 will do. If you are eager to learn with the second endpoints for nGBM is

https://investorshub.advfn.com/boards/read_msg.aspx?message_id=169688051
EU/UK and US endpoints do not differ

EU/UK/
The first secondary objective is to compare overall survival (OS) between patients randomized to placebo who received DCVax-L treatment following disease recurrence and control patients from comparable, contemporaneous clinical trials, in patients with recurrent GBM.

US
1. The first secondary objective is to compare overall survival (OS) between patients randomized to placebo who received DCVax-L treatment following disease recurrence, and control patients from comparable, contemporaneous clinical trials, in recurrent GBM.
[ Time Frame: Until death ]

exact the same
It has been stated more than once by the company and LL that the SAP is the same with every RA
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