The MK trial may miss the OS P value 0.05, but may produce 5 year ~65% Vs ~60%, a 5% advantage of HR 0.95, good safety profile
Could you explain the mathematics and statistics that led you to arrive at that outcome?
How does your estimated result coincide with how many of the 298 events are SOC, how many are MK treated patients and how many are SOC and MK treatment dropouts (LTFU)?
Do you seriously believe that with a weighted average of 5 years on trial, an estimated minimum of a 55% rate of events for SOC patients and a result documenting that only 37.5% actually evented, this trial will fail?
Failure is only possible if the trial has an enormous number of LTFU (perhaps more than 20%) and I don't believe that we have even one quarter of that number.