RE: Facts P14027 Nov 2025 08:40
Again, xviolet, very selective use of facts. Thank you for conceding that the FDA recognises p140 as a late stage asset. Humira was also a late stage asset with a failed trial behind it, and we know what happened there. The key is in trial design. New diagnostics, better understanding of moa, higher dose etc. All good reasons to believe a result could be different this time. Also thank you for conceding that there is large and growing interest in the autoimmune space, that multiple CDA’s have been signed, that HLK have processed a new patent application with potential to add 20 years patent life, shall we add that company is funded for the foreseeable?! Etc … I recall you being uncertain at 2p as well. IMO DYOR GLA