Thanks to the other moderators for responding, quicker than I could.
What I will add to their responses:
There are two things going on here...
1) We have existing drug
2) We are making more drug
So, for point 1:
We have enough drug in hand that we can supply the Phase 2 trial in South korea
So, for point 2:
We hired a chemical company in the USA to not only make more Ifenprodil for us but also look into making it in a more streamlined fashion.
Additional point:
We are going to secure IP on a novel formulation for IV use.
The implications of this go beyond our trials. If others want to use it by IV, they will be going through us.