Agree we need P2 to maximise any deal and timeline is years off so patience is required. That’s what the Cosela (example) and Race trial timeframes / triangle report suggest.
P1 results will give insight into proof of concept for CPACS and thus a ‘major’ turning point in the development of RC220.
If you think P1 is ONLY a safety trial then think again. If CPACS isn’t present in P1 then I’m doubtful P2/P3
would show otherwise.
This is due to the way Cardio protection and FTO inhibition work.
Cardioprotection thread, page-436
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