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manibiotech

06/28/25 1:24 PM

#773306 RE: dennisdave #773296

I agree . And I read a year or two ago ( can't remember if in a PR, filing or a presentation / video transcript) that NWBO used a consulting firm to develop their ECA and NWBO has no invoIvement in it , so it was completely independent . Very stringent measures/ guidelines were used.  I am forgetting  name of the firm, but I researched at that time and it is a reputable large firm in UK which has worked with MHRA in the past . So they did their due diligence in that respect . But on the same token,  if I remember correctly there have been GBM trials which have used patient level data . But I agree that issue should have come up much sooner last year . 
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kfa670

06/28/25 4:51 PM

#773334 RE: dennisdave #773296

Hello Dave,

For fun, if you threw a dart at the calendar for a day after June 30, how long/what day would you pick for the MHRA to have considered all the "public comments" and make a decision?

For fun!