Drug development and commercialisation is all about meeting regulatory requirements, hence clinical trials (end point, mid point, beginning point, any point) and at the end it boils to one thing: data.
AIPAC data will not be the end or all, but is pivotal. IMO, we will survive even with poor AIPAC data. This is because: Efti (or Lag3 related drugs) have shown a strong safety profile and it represents a key aspect of immune system.
And we have patents.
It will happen, next week may well be turning the corner for us, if not, I am patient. We have other trials going, not just AIPAC. We are not a one pony company.
News: IMM Immutep Receives Positive EMA Scientific Advice For Further Clinical Development Of EFTI..., page-19
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