Lots of words with no examples or data. Long winded.
The slide from CHM had 7-10 years from start of phase 1 to FDA approval. So if Vaxinia gets FDA approval 3-4 years from now (say 4-5 years from start of phase 1), that would be outstanding.
Lets say they do an expansion cohort for bile duct and complete that by the end of this year 2024. All goes well, FDA says go straight to a registrational phase 2 trial, which IMU had aleady designed. Takes another 12-18 months to enrol that with rolling results and not waiting for mOS, using response rate and maybe mPFS instead. Also rolling submission to FDA. Results and submitted by H2 2026. Fast FDA approval time of only 3-6 months, H1 2027.
Again, as a shareholder I would be happy to be wrong in this case. But I reckon many people here are in a fantasy land. No wonder the SP can be so volatile.
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