As you have no idea about future revenue, nor about the value of JVs you have given a very compelling argument which leaves out key data.
You can't disregard this as a key factor. What's quite frightening is your willingness to do so.
Also where is your evidence that trial results will be negative? I assume you only mean the key trials in advanced stages, as it would be silly to assume that any trials over any applications.
And if you look at the catheter delivery system for CHF which have been posted about many times, and the increased access to patients with that delivery system how on earth do you imagine that there is a serious risk to efficacy?
I mean, already CHF has proven efficacious to the most costly CHF group, those with advanced CHF. These patients are normally hospitalised. But MSB's application has already been proven to work in Stage 2, all that's needed are the increased numbers. So that makes the CHF application highly valuable.
Plus Japan is going to work off the Stage 2 FDA results, and have a small clinical trial of only 10-20 japanese people. But the treatment works high up the biological chain, the DNA of japanese people isn't going to change the efficacy. This is not drug treatment which is lower down the biological chain and therefore fraught with uncertainty. How do you imagine that small trial is going to fail?
Among the barrage of selective facts, and misleading statements available in chatrooms, the danger is that people will rely on them. This is why there is a disclaimer when you sign on. DYOR people. If you have any problems putting this in perspective, call the company and get a balanced view. Julie Meldrum is there for Investor relations and she will get back to you if she can't speak immediately.
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