Home > Boards > US OTC > Biotechs > NorthWest Biotherapeutics Inc. (NWBO)

I know we all stress the TLD, Journal

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skitahoe   Tuesday, 09/14/21 03:28:39 PM
Re: None
Post # of 424233 
I know we all stress the TLD, Journal publication, etc. but one document is really what matters in terms of when DCVax-L can be approved, that's the BLA. I believe we may have sections of the BLD under review in a rolling BLA with one or more of the regulators, but whether that's true or not, completing and submitting the BLA is the key to approval, the rest is icing on the cake.

As for AdamF and others who've been the vehicle for shorts, I believe the evidence of success will be so overwhelming that they'll try to paint an entirely different picture once it's revealed. I can imagine AdamF trying to say he called everyone's attention to NWBO, and while his views were negative, he'd never have called attention to the company if he didn't believe it had great potential. Investors should thank him for calling attention to the company and investing after the price was driven down by his and others actions. He'll rate it a great buy now.

I know it's frustrating, but NWBO management is building a solid case for approval, when it's revealed I believe all doubts will be removed and it will be hard to say just how high the stock may go. Of course if either a partnership or buyer comes into the picture it could go much higher than if nothing is said.

It's my belief that it's possible that roughly at the same time TLD is submitted, a Journal publication is released, the manufacturing facility is approved, the big surprise may be that the BLA has been submitted to the four regulators and we get PDUFA dates. I certainly could be wrong, but we're approaching a year since the company should have received the data from it's contractors, I believe the BLA ought to be pretty nearly finished.

Gary

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