My major concern with N is not the 25. I was content with the toxicity/safety end points of P2. That the secondary end point promises possibly tremendous efficacy is highly interesting.
But, what of the 7? Fully 21% of the initial group dropped. The Overall demographics were younger and more moderate stage than mean statistics from previous trials.
I am anxious for all the hyperbole to be tested in an FDA approved and Market satisfying test group population P3. That will take money and TRUE interest from a marketing/production savy BP. I can wait, but I won't bet the house.