RE: All markets Asia Summit28 Oct 2021 10:17
More positive news about the pipeline today with 523 going straight into a registration study. The supporting data to be presented in a few weeks in America.
If all goes well that should complete early 2023, NDA late 2023 approval late 2024 and sales in 2025.
As shown by that indicative timetable, the main risk for HCM is competition moving the standard of care on (which is a good thing for patients) but it could limit the returns on investments.
We seem to be in a sectoral slump at the moment - only 6 months to go to the PDUFA date for surufatinib in the US. The first of many significant dates, but one that will confirm HCMs potential.