CEO avsluttet jo presentasjonen med å si noe relevant om dette:
“We look at each indication per se, so with NIPU positive data we will be discussing with the authorities the possibility of orphan drug designation, breakthrough designation, the potential for accelerated approval, discuss the next stage of development and use that as supportive data for the other indications. […] INITIUM and FOCUS are not that far away, but our approach is that each indication has a value per se, and each positive data strengthens the profile of UV1 as a treatment that can be used in multiple cancer types and in combination with different treatments. There is always going to be a tradeoff between when the data is available and the initiatives, but what I can tell everybody is that we are not going to be waiting for the results from all three studies before we initiate activities. […] As soon as we have the data there are a series of initiatives that are triggered immediately”