I certainly didn't miss any of that, as well as the reactivation. You and others can explain the science a hell of a lot better than me. The wording "blurring the lines" and enabling this to move "faster" is enlightening as well as exciting. I'd like to get as many patients enrolled as we can that fit the profile they're looking for of course. This is excellent news and follows how you've been talking about proceeding. That's why I follow you and a few other science types!
My guess is ovarian cancer. Besides the lesion disappearance case, CTIX shared an interview by BioCentury TV with the FDA last month. The director of oncology said for future ovarian cancer trials, the FDA is only asking for one arm and overall response rate, instead of the traditional multi-arms and overall survival rate. This will expedite the Kevetrin Phase 2/3 trial tremendously. Imagine administering Kevetrin at 750 mg/m2 daily for multiple consecutive days. The response rate will go through the roof!