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News Focus
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newman2021

05/31/24 11:18 AM

#695184 RE: StonkMaster #695182

They had a meeting whole day on March 5th; what was that about?? Does NICE want the Approval as the evidence?? is that how it works?? what is evidence as it relates to NICE?? Anyone???
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Nemesis18

05/31/24 11:24 AM

#695188 RE: StonkMaster #695182

>>>Directly from NICE, dated today:

"The next step would be for the company to let us know when they would be able to send an evidence submission to NICE. There is no further update at present."<<<

When will you greedy feckers here realise that your hard earned money invested here is in jeopardy?

This isn’t a game. Now you seriously need to think about where you would be if you lost everything!!
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kfa670

05/31/24 11:24 AM

#695189 RE: StonkMaster #695182

Just my train of thought...

But why would NICE waste precious time and resources on an appraisal for DCVAX, before it was guaranteed that DCVaX was an approved and available option.

It also makes sense to me that an appraisal, once MHRA approved and all submission evidence is in hand, shouldn't really take that long. They are analyzing the cost feasibility. Not 1.7m pages of trial data.

Hence a quick decision by NICE once MHRA approval and evidence e submitted by NWBO.

Maybe? 🤔
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beartrap12

05/31/24 11:53 AM

#695201 RE: StonkMaster #695182

This is what's on NICE from March 5, 2024:


Date Update
05 March 2024 A meeting was held between NICE and the company in early-February regarding next steps for the appraisal of DCVax-L for treating glioblastoma, and more information will be available in due course. NICE will continue liaising with the company and monitoring timelines.



StonkMaster, this has been on the NICE board since March 5, 2024. That's almost 3 months ago. Plenty could have happened during that time.
Bullish
Bullish
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iclight

05/31/24 1:05 PM

#695248 RE: StonkMaster #695182

I’ll bet the evidence NICE wants includes patient level data for the control arm, just like the FDA requires. Whoops! Eternal delay for that.