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Re: alexander77 post# 15613

Sunday, 03/12/2017 2:22:23 PM

Sunday, March 12, 2017 2:22:23 PM

Post# of 18784
I agree with the assumption that if the FDA approves Zoptrex for endometrial cancer, then it will very likely pave the way for the same drug to get approvals easier and sooner for other applications as well.

The share price thing is really all conjecture. And the history of this company isn't great.

For me right now I would very much like to see baby steps, meaning lets see if the FDA overturns there original denial of Macrilen. Which they will only do if they agree that there is enough positive evidence of this drugs capabilities while over looking the fact that it narrowly missed an end point. Believing there is enough good with the ease of testing the safety compared to the ITT and results of test that are as good or better than the ITT. I feel if the first domino falls in the way of the company giving them a real revenue stream then it will be easier for the next domino to fall there way.

Just my two cents. Obviously we all know that Zoptrex has the much, much higher ceiling and the FDA seems to really like safety, and the fact that this appears to have a great safety profile it could help along with gov't supposedly looking to ease approvals.

As far as dilution I personally hope that if Zoptrex does pass the European company that AEZS is supposedly in negotiations with will supply an upfront payment large enough to fund bringing both products to market. Whether that is a likely scenario I don't know. But the company did say they were in negotiations and wanted to wait for results as it would put them in a stronger position.

Of course it could all the wrong way and we're all phucked. except for the nay sayers and shorters who will be in full force saying I told you so. Either way we will know within 30-60 days the whole truth of it.

Fingers crossed
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