海角精品黑料

FDA plans ultra-fast review of three psychedelic drugs following Trump directive

WASHINGTON (AP) 鈥 The said Friday it will offer ultra-fast review to being developed to treat mental health conditions, including depression, the latest step by the Trump administration toward possible approval of the .

President Donald Trump last weekend directing the FDA and other federal agencies to speed research and loosen restrictions on psychedelics, a class of hallucinogenic drugs which remain illegal under federal law.

The FDA said it awarded to two companies studying psilocybin 鈥 the active ingredient in magic mushrooms 鈥 for hard-to-treat forms of depression. A third company received a voucher for methylone, a drug related to , for post-traumatic stress disorder. The FDA did not name the companies in a press release announcing the news.

鈥淲e owe it to our nation鈥檚 veterans and all Americans who are suffering from these conditions to evaluate these potential therapies with urgency,鈥 FDA Commissioner Marty Makary said in a statement.

The vouchers don鈥檛 guarantee approval, but instead mean that regulators will try to shorten their reviews from a period of months to weeks.

The recent moves on psychedelics reflect growing among Trump鈥檚 supporters, including and followers of the spearheaded by Health Secretary Robert F. Kennedy Jr.

Last July, Kennedy told members of Congress his department aimed to for hard-to-treat psychiatric conditions within one year. Some of Kennedy鈥檚 top allies and staffers are proponents of the drugs.

, a former Kennedy campaign staffer now serving as a senior health adviser, has previously written about the 鈥渕ind-blowing鈥 power of psychedelics and his plans to invest in companies developing the drugs.

FDA’s special treatment for psychedelics is likely to renew scrutiny of its program for speeding up drug reviews, known as the program.

have noted that vouchers have gone to companies that are politically favored by the White House, including those that have agreed to cut prices on their medications.

In a separate move, the FDA authorized initial testing of a drug related to ibogaine, a powerful psychedelic made from an African shrub, for people with alcohol use disorder. Ibogaine is known to sometimes cause dangerous heart rhythms but has been embraced by combat veterans as a way to treat trauma and addiction.

The drugmaker, DemeRx, is led by a Florida-based researcher who first began studying ibogaine as a treatment for cocaine addiction in the 1990s, before federal health officials pulled funding for the work.

鈥淓very grant proposal that I submitted to (the National Institute on Drug Abuse) was rejected,鈥 Deborah Mash, a neurologist and founder of DemeRx, told The Associated Press. 鈥淚 couldn’t get that funding and that’s why ibogaine didn’t advance in the 1990s.鈥

Ibogaine is known to cause intense hallucinations, nausea, vomiting, tremors and sometimes dangerous irregular heart rhythms. Mash says DemeRx鈥檚 drug is a metabolite of ibogaine, and doesn’t carry the same hallucinogenic effects or risks as the original drug.

Saturday鈥檚 White House event on psychedelics suggested Trump鈥檚 political allies had a role in pushing the drugs to the top of his agenda.

, the podcaster who appeared at the Oval Office event, said he texted Trump about the psychedelic ibogaine, which he鈥檚 repeatedly discussed on his show. According to Rogan, the president quickly responded: 鈥淪ounds great. Do you want FDA approval? Let鈥檚 do it.”

搁辞驳补苍鈥檚 days before the November 2024 election was seen by White House aides as a key factor in his election victory.

On his show earlier this week, Rogan said he learned about ibogaine from his friend Ed Clay, a mixed martial arts trainer and entrepreneur who runs retreats making use of it in Mexico.

Virtually all psychedelics, including LSD, psilocybin and MDMA are classified as Schedule I substances, a category for high-risk drugs that have no medically accepted use.

For decades, drugmakers steered clear of the substances due to the difficulties of studying drugs that are illegal under federal law.

But dozens of small drugmakers, many fueled by Silicon Valley investors, have recently jumped into the race to win FDA approval for various psychedelics. For example, 鈥 who has made political donations to both Trump and Vice President JD Vance 鈥 has invested in AtaiBeckley, a company studying MDMA and other psychedelic compounds.

___

The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute鈥檚 Department of Science Education and the Robert Wood Johnson Foundation. The AP is solely responsible for all content.

Copyright © 2026 The Associated Press. All rights reserved. This material may not be published, broadcast, written or redistributed.

Federal News Network Logo
Log in to your 海角精品黑料 account for notifications and alerts customized for you.