So one million dollar question, I guess. To date, we have no data to compare in a comparison between all ADCs. So that’s really difficult to answer. But if we base our results on the A3 study that was published last year by Dr. Abelman, we can see that sometimes changing the target can bring an additional benefit as compared to having the same payload. Hopefully, one day we will have ADCs with different targets and different payloads at the same time...
So one million dollar question, I guess. To date, we have no data to compare in a comparison between all ADCs. So that’s really difficult to answer. But if we base our results on the A3 study that was published last year by Dr. Abelman, we can see that sometimes changing the target can bring an additional benefit as compared to having the same payload. Hopefully, one day we will have ADCs with different targets and different payloads at the same time. It will be really easy when someone is going to progress with an anti-Trop2 and anti-topoisomerase 1 ADC, maybe to change all the target or both payload and target. But unfortunately, for now, the ADC development is based mostly on topoisomerase-1 inhibitors. So we’ll have to change the target. We will have definitely to change the payload first, but it will depend on the molecules that we will have.
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