What is that common "issue."
If it is failing phase 3 trials, that's not unique to stem cell companies. That's drug development in general.
If it is post hoc analysis, I would remind you that our big problem has been failing primary endpoints when looking at entire cohorts. We have shown statistically significant results on pre-specified subgroups, and also across entire cohorts for some secondary endpoints. This is not post hoc analysis.
Any post hoc analysis we have done has been clearly labeled as exloratory.
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