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Re: skyhigh50 post# 114989

Tuesday, 02/04/2020 9:12:15 PM

Tuesday, February 04, 2020 9:12:15 PM

Post# of 144823
January 27th came the news all tests were successful

That’s only 10days ago. It was fantastic news.

We asked the company for clarification on the patents. We just got that. Great to be getting feedback from them.

Austrianova needs to issue the paperwork.

It needs to be incorporated into the ind.

They need to do all proof reading and maybe some adjustments.

Facet needs to slot us into their schedule to get everything done.

Do they need to raise the funds to submit it?

I don’t think a few weeks is too long for all of that.

Let’s relax and let them do their jobs.

Why aren’t they giving us a date? Probably because they can’t be sure when it’s going to be completed and if they give a date and miss it we’ll all be on their backs and the share price will go down. So it’s good they don’t do that. What they expect and how long it will be are different things.

They did what they said they’d do with the manufacturing runs and tests.

They were successful. They kept at it and brought new expertise and did run after run until it was perfect.

That’s what they’ll do with the ind too.

If it takes another month it’s fine. Better to be perfect than flawed.

I have every faith in them to successfully submit the ind when it’s ready too.

No amount of fear or panicking is going to make that faster.

Just like the manufacturing runs, they will be careful diligent, scientific and legalistic in their preparation of the ind. they’re not going to rush it at this stage and maybe cause greater delays later.

The tests results were real. Independent. Exactly how the cells need to grow and trigger the ifosfamide.

They were successful despite our impatience, fears and doubts. There was nothing ‘mythical’ about it.

The ind submission will be just as successful.

They’ve only had final results for ten days. Ten days.

This is a novel and unique cancer therapy from a tiny biotech. It’s going to inject live human cells from a human into other humans. They need to submit the most thorough, carefully thought out, perfect application to be able to get the fda to let them do that.

And they need to impress them with their professionalism, care and thoroughness.

And they need to impress dr Hidalgo and the many clinics And doctors who will conduct the trials as well.

This is medicine. This is peoples lives. This is the fda.

This isn’t a pump n dump scam.





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