News Focus
News Focus
Followers 24
Posts 4176
Boards Moderated 0
Alias Born 12/18/2019

Re: GPha post# 499797

Monday, 08/01/2022 2:59:07 PM

Monday, August 01, 2022 2:59:07 PM

Post# of 822990
NWBO and clinicians had no reason to unblind recurrent patients. They had all signed an informed consent for a NAIVE GBM trial (the original protocol) and that protocol specified that EVERY patient that had recurrence would be offered a rescue treatment.

Here's the clinicaltrials.gov:
"All patients will have the option to receive DCVax-L in a crossover arm upon documented disease progression. (note: DCVax-L when used for patients with brain cancer is sometimes also referred to as DCVax-Brain)"

Otherwise they would drop out of the trial. There is NO need to unblind patients at anytime in this trial.
Volume:
Day Range:
Bid:
Ask:
Last Trade Time:
Total Trades:
  • 1D
  • 1M
  • 3M
  • 6M
  • 1Y
  • 5Y
Recent NWBO News