Is it obvious? As I said its beyond my grasp yet to understand. Its not black and white that its just bad trial design that has caused the failure of the primary end point- the cohort selected, clinical outcomes expected and the sample size all interplay to hopefully avoid false results.
There is huge academic debate over clinical trial design and appropriate primary end points argued by much smarter people than me. Until there was a contradiction in primary and secondary outcomes I never delved into it - wish I had.
The trial design is a convenient explanation for the seeming contradiction of the two outcomes in the announcement. Another possibility is that OPFS has achieved clinical improvements but failed to do so with enough statistical confidence Until we have the data we don't know.
were the patients who had liver + others mets treated with Spheres only or spheres + chemo? ethically you couldn't deny an effective treatment to experiment with another so you would do standard + test compared to standard only and look for a difference. I don't think they were looking to treat extra-liver mets with spheres at all, more looking to supplement the chemo with the liver targeted therapy.
craft said:But I know enough to know there is more to the story then just somebody making a nieve mistake in trial design.
This has been a very informative thread. I thought Tuesday was an overreaction and it appears that that is the consensus.
Hurried back up a fair bit this morn... Up 36% although I do not completely understand why from the announcement
Was this announcement out of the blue or was there some way of knowing when it was coming?
I thought there would be no updates until late May.
The abstract result clearly showed that the contents were market sensitive... and obviously SRX knew about its content before the abstract release.
Question:
Why does the ASCO meeting guidelines / rules trumpt the ASX disclosure rule?
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