RE: Future of HCM18 Sep 2020 09:00
Another good post, Jatw. Thanks.
To my query of low market valuation despite a deep pipeline, you seem to think ‘not owning a first line therapy’ could be one of the reasons. Would Surufatinib be able to fill that void to a little extent? As per information provided yesterday by the company in relation to the second NDA acceptance by the authorities, it is mentioned ‘there is no effective therapy’ in China for advanced Pancreatic NET. It also says ...’In the U.S., the Food and Drug Administration (“FDA”) granted Fast Track Designation status to surufatinib for both the non-pancreatic NET and pancreatic NET development programs in April 2020. Chi-Med has initiated preparatory work for the U.S. NDA and intends to utilize a rolling submission, which is expected to start in late 2020. In addition, the Marketing Authorization Application (“MAA”) submission in Europe is planned for 2021’
We can, at least, keep our fingers crossed! Of course, we are following a faster tortoise and not a hare!!
Btw, on stockwit site, yesterday’s post- market sp of ADRs has gone up by $1.74 or 5% raise! I doubt if it is accurate.