My first question is for Dr. Campbell.
If I have this wrong, please correct me, but in your opening comments you mentioned that you had worked with some pharmaceutical companies. One of the things that is obvious to me—but I want to get your perspective if you're able to give it—is that with these drugs there are so few people who are actually going to take the drug or benefit from it that the pharmaceutical companies say, “If we can do it through the SAP program, we will.”
To me, if it's been on the SAP program for 20 years, we should have a system whereby we make it very easy for these pharmaceutical companies to move it into a registered drug. Do you have any comments or thoughts on this idea—that we should do less through SAP and have more registration?