Sorry, you're wrong. I work in FDA compliance so I happen to know a little more about this subject. There are PLENTY of provisions in the CFR (Code Federal Regulations) governing use of experimental or not fully tested drugs on terminally ill patients. Look up "Compassionate Use". A miracle drug that saves 1/3 of hospice patients from cancer would certainly be funded by a biotech/pharma company or the US government. But guess what, drugs cannot under any circumstances go to large-scale populations because if they are untested, you will end up killing more people than you save. In your example, sure the drug may have saved 1/3 of hospice patients, but it very well could have caused the other 2/3 of them to die faster, or suffer a stroke, or whatever. Unless these risks are known, its completely irresponsible for the government to allow it to go into widespread use without a proper clinical trial. There are very valid reasons to the FDAs laws governing drugs. There is no evil boogyman that is trying to prevent miracle drugs from coming to market.