The latest proactive video is definitely worth watching.
LC Suggest that they have all the data, are now going to review the Her Vax data, including blinded radiology review, which will help independently verify progression free survival status for each cohort. I suspect IMU will then look at an FDA submission for Her Vax (She says as much in the interview).
This would be a logical/ necessary step in de-risking any partnership/pharma deal which may evolve beyond this point.
It is also implied in the commentary that, given there are such a small number of patients in the trial, a significant difference in PFS between "treatment" ie HerVax/Conventional treatment versus conventional treatment alone exists. Otherwise smaller differences would require a higher "powered' study, ie greater number of patients to see smaller differences.
IMHO K
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