美国食品药品监督管理局快速审批致幻药物,最早可能在夏季获得首次批准。
FDA Grants Quick Review Psychedelic Drugs, First Approvals Could Come As Soon As Summer

原始链接: https://www.zerohedge.com/markets/fda-grants-quick-review-psychedelic-drugs-first-approvals-could-come-soon-summer

美国食品药品监督管理局(FDA)正在加速研究针对严重精神健康状况(如难治性抑郁症、创伤后应激障碍和物质使用障碍)的迷幻药物治疗,此前美国前总统特朗普发布了一项行政命令。专员马蒂·马卡里表示,首个迷幻药物的批准可能在夏季结束前获得。 FDA将优先考虑显示出早期希望的药物,为专注于如赛洛西宾等化合物的研究公司提供激励,并已批准美国首个诺比加因临床试验。特朗普的命令拨款至少5000万美元,鼓励机构之间(包括退伍军人事务部)共享数据,并旨在简化已批准药物的重新归类程序。 虽然官员们承认这些治疗方法具有“改变生活”的潜力,但他们强调这些治疗方法*尚未*获得批准,并将接受严格的安全和科学评估。这一消息已经对迷幻疗法行业的股票产生了积极影响,预示着主流兴趣日益增长。

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原文

The FDA announced new steps to speed up research on psychedelic treatments for serious mental health conditions, following an executive order from President Donald Trump directing agencies to expand access to emerging therapies, CNBC and NBC reported this morning:

In a press release Friday, FDA commissioner Marty Makary said the medications “have the potential to address the nation’s mental health crisis, including conditions like treatment resistant depression, alcoholism and other serious mental health and substance abuse conditions.” On Monday, Makary told NBC News that with the accelerated application process, the FDA could potentially approve the first psychedelic drug by the end of summer.

The agency said this effort could support new treatments for conditions like treatment-resistant depression, PTSD, and substance use disorders. Measures include prioritizing drugs with early promising results and offering incentives to companies studying compounds such as psilocybin and methylone. It also approved an early clinical trial for noribogaine, marking the first time a drug of its kind will be studied in the U.S.

Officials emphasized that these actions do not mean the treatments are approved or proven safe. All research will be closely monitored to ensure it meets strict scientific and safety standards.

Popular psychedelic names like Compass Pathways and AtaiBeckley have turned positive YTD on on the news out the last few days.

"The executive order I'm signing, we're actually signing the executive order today, is really a moment," Trump said at the signing event days ago. "These treatments are currently in the advanced stages of clinical trials to ensure that they're both safe and effective for the American patients."

Trump's order, signed on Saturday, directs the FDA to prioritize review of certain breakthrough-designated psychedelic therapies, expands potential access under the Right to Try Act, commits at least $50 million in federal funding for state partnerships, and encourages closer coordination among HHS, the FDA, the VA, and private-sector researchers.

"In many cases, these experimental treatments have shown life-changing potential for those suffering from severe mental illness and depression, including our cherished veterans," Trump said, citing the veteran suicide rate.

The order also instructs the Justice Department to move quickly on rescheduling any psychedelic-based product that successfully completes Phase 3 trials and receives FDA approval.

Trump continued, "And the nice part is we're actually doing this early, but it has been going on. Research has been going on for quite some time. But, you know, usually with things like this, nothing ever happens, no matter how the research ends up, but we're changing that. This order will clear away unnecessary bureaucratic hurdles, improve data sharing among the FDA and the Department of Veterans Affairs, and facilitate fast rescheduling of any psychedelic drugs that become FDA-approved." 

As we wrote days ago, these stocks are starting to go 'mainstream' after being ignored and out of the limelight for years. Zero Hedge contributor Quoth the Raven has named the sector his “best idea” sector for 2026.

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