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Re: Pyrrhonian post# 39402

Wednesday, 08/26/2015 2:38:01 PM

Wednesday, August 26, 2015 2:38:01 PM

Post# of 688913
Okay, so I looked at the PR and SEC statement again and they are preparing to submit something from the "trial", so I was wrong on that. But that submission still doesn't mean that it's due to the screening halt. It's not necessarily a cause and effect, but maybe it's just a next step. The 300+ enrollment indicates the trial screening pipeline likely is full and I expect we will hear that in a few weeks. The company on SEC record where they state that some bloger is trying "to turn good news into bad news". To me they would never make a comment like this if they were submitting a safety. Never. I seriously think you should rule safety out. As for what they're submitting, maybe it is something positive. Even if you personally can't see AA or EAMS, hopefully you can at least see something like Fast Track using the data on the 55 compassionate arm to get that designation.

http://www.nwbio.com/nw-bio-confirms-phase-iii-trial-of-dcvax-l-for-gbm-brain-cancer-is-ongoing/

http://files.ctctcdn.com/6125bf3f301/9e1f334b-929e-4926-a6c4-fb5127bfa4e4.pdf
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