me, you, all of us... Oh, you mean to run the trial. Good point....

me, you, all of us...

Oh, you mean to run the trial.
Good point. If only we had a management team that could engage the experts in the field globally as well as key research & industry leaders across the complete logistics and scientific domains... then again, i am adreamer.

Enough joviality, I too want to know that and i do have confidence there is a very well considered plan. For now they have the capital to build an appropriate team but we all know it is insufficient to execute to full trial. Waiting on ODD is probably likely as others have stated as it has commercial substance.

Bringing on this guy ticks the regulatory boxes (I am guessing he is not full time) but also adds expertise. I am impressed for what it is worth.
As a potential backer or partner, having a strong stable is going to give higher confidence.
Let's not forget, with almost nothing in recruitment for trials to support ALS/MND, there will be more patients than usual available for trail. We all hope we can get to 210 patients and it not take a year!
Then, if we get to 24 weeks plus a couple of months to get all the data, we could be going to commercial use. For those of us that have painful memories of manufacturing MPL, we don't want/need any hickups. So having ole mate Herbie join us might be our uber to quick FDA interim approval to go to market.

I swear that is Michael driving and John Clark navigating with Herbie getting them there.