Yesterday, the FDA issued emergency use authorization for hydroxychloroqine and chloroquine to treat COVID-19. Politics, not science, is why.
St. Elizabeth Healthcare in Cincinnati recently accepted $5 million from dōTERRA, an MLM company selling essential oils based on dubious claims. This is most definitely not a good look.
Richard Jaffe was Dr. Stanislaw Burzynski’s lawyer. For nearly two decades, Jaffe defended this cancer quack from the FDA, Texas Medical Board, and the government in the name of “health freedom” and even invented Burzynski’s business model of having over 70 clinical trials open that allow him to treat any cancer patient he wants. More recently, he’s been a defender of for-profit quack stem cell clinics. Last week, he shocked me by finding one stem cell clinic so quacky that he thinks the government should shut it down, even going so far as to use criminal prosecution if necessary. Basically, he’s willing to throw one quack stem cell clinic under the bus, so that others can continue to profit.
“Right-to-try” laws are a cruel sham that purport to allow terminally ill patients access to promising experimental drugs. In reality, they strip away many protections and leave vulnerable patients on their own. After four years and a number of toothless state laws, a federal version of “right-to-try” has passed Congress and is poised to become law. Once President Trump signs the bill this week, this federal version of “right-to-try” will leave terminally ill patients on their own and will likely be the first step in returning the FDA to its pre-thalidomide state, in which it only required evidence of safety, not efficacy, to approve drugs.
Last year, the FDA announced a regulatory framework for stem cell clinics, and hopes were raised that it would finally crack down on the hundreds of quack stem cell clinics in the US. Yesterday, the FDA dropped the hammer on two clinics, seeking injunctions in federal court to stop them. Is this the beginning of a real (and long overdue) crackdown on these clinics?