The U.S. Food and Drug Administration (FDA) is warning about “vampire” treatments that involve injecting plasma from young donors in an attempt to reverse aging, saying it hasn’t been proven to have medical benefits.
The procedure works as follows: People are infused with the blood from young people, and clinics claim that the procedure is like a fountain of youth. Claims include slowing memory loss, aging, dementia, and a whole host of issues.
“The reported uses of these products should not be assumed to be safe or effective,” he added, saying that the FDA strongly discourages people from using this treatment.
“Outside of clinical trials under appropriate institutional review board and regulatory oversight,” they shouldn’t be used, he said.
The commissioner added there are “a growing number of clinics” offering plasma from younger donors.
“Treatments using plasma from young donors have not gone through the rigorous testing that the FDA normally requires in order to confirm the therapeutic benefit of a product and to ensure its safety,” he added. “As a result, the reported uses of these products should not be assumed to be safe or effective.”
Company Shuts Down
According to NBC News, Ambrosia, a “young blood” company, said it had “ceased patient treatments.”Ambrosia, based in California, charged $8,000 for a liter of blood and $12,000 for two liters as part of a clinical trial.
The blood was donated by 16- to 25-year-olds to people over the age of 35.
Jesse Karmazin, 34, a Stanford Medical School graduate, stated the firm several years ago. He began a clinical trial and claimed it produced impressive results.
“Young plasma is the result of research into the science of blood,” the website reads.
“You can easily imagine a situation where somebody who’s vulnerable, and not wealthy, and not healthy, and may be desperate ... would potentially feel like they have no option but to spend this money,” said Phuoc Le, a doctor who teaches at University of California, San Francisco, according to the Huffington Post.
So far, the FDA didn’t say whether it will pursue enforcement actions against firms offering the treatment.