TSXV:CLAS.H - Post by User
Comment by
Oenophileon Oct 28, 2020 8:11pm
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Post# 31800529
RE:RE:RE:The smart ones did not sell their shares..
RE:RE:RE:The smart ones did not sell their shares..Might Kalytera have enough data to release their GvHD therapeutic in the EU with a post market trial? Phase 3 only required 25 patients. They pretty much approve anything in Europe - look at NeoVasc's device for refractory angina. EU approved 8 years ago, FDA advisory committee completely trashed their presentation/data yesterday. Might also try compassionate use in the US? Trying to be positive about this. Still think R107 for Covid is worthless.