I will set you a challenge then to declare."Everything I am...

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gavint66

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25/06/24

20:41

Post #: 74486352
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Originally posted by Bazsa: ↑

Looks like it is easy to put those with different points of view in suspension while continuing the lies. A three to four fold increase in the significance of a study due to much larger population being assessed and you still continue with the low N value bull . 11 lots were tested, howmany would you say were needed?

(we can hold in suspension Bazsa's suggestion that there may be more than one patient per data point - so each of the 11 might be an average - (with 2 patients behind one data point perhaps 3 behind another perhaps all adding up to say 40 at the max (but its less than that though because you can't include subjects who got multiple lots - this is still only single lots (that's written on the slide) I can deal with that later multiples per dot suggestion of Bazsa's later I think)."[

Are look at the P values, how could they be so different ?
Glad to see I am not the only one to be put on suspension when the facts get in the way of a good story

chahttps://hotcopper.com.au/posts/74182160/singlenge?

"which is the onlypotential adequate and well controlled study (the FDA is supposed to have at least one for a BLA"

Well done, that makes 3 piles of bull in one post.

I really do wish you a good trip to the cliff face.

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I will set you a challenge then to declare.

"Everything I am researching says beware of tumorous cell splitting mutations?"

That is my statement so I now want you to declare that there is..... no possibility of tumorous mutations with iPSC therapy?

Declare it with proof of actual therapy in humans and we can move on.

I get it that we all see stem cells as the golden ticket.

Some are just a bit more greedy and the FDA need to go with nature before artificial when something is new to approval.

Last edited by gavint66: 25/06/24

CYP Price at posting: 28.0¢ Sentiment: None Disclosure: Not Held
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