Showing posts sorted by date for query MDMA. Sort by relevance Show all posts
Showing posts sorted by date for query MDMA. Sort by relevance Show all posts

Sunday, September 06, 2026

 

New Zealand approves party-drug MDMA for treating patients with PTSD

MDMA is a well known party-drug.
Copyright AP Photo

By Simon Ormiston
Published on

Two psychiatrists in New Zealand can now prescribe MDMA in controlled clinical settings, built on trial results that have been challenged in the US.

Two New Zealand psychiatrists have won approval to prescribe pharmaceutical-grade MDMA to patients with severe post-traumatic stress disorder, making the country only the second in the world - after Australia in 2023 - to authorise the party drug for clinical use

New Zealand's medicines regulator, Medsafe, granted the approvals to Wellington's Dr Gary Wynn and Auckland's Dr Tom Paterson, who spent more than a year passing the regulatory process.

"PTSD ruins lives and is difficult to treat," said Deputy Prime Minister David Seymour, who last year backed a similar approval for psilocybin, the active compound in magic mushrooms, to treat severe depression.

"MDMA can be very effective at treating it through psychedelic-assisted therapy," he said, adding that New Zealand remains committed to opening access to "innovative treatments."

PTSD develops after a person experiences or is threatened by traumatic events such as combat, sexual assault or sudden death.

Existing pharmaceutical options in most countries are limited to two antidepressants that can take three months to take effect and produce uneven results.

The evidence behind the approval — and why the US said no

The approval draws on evidence from two pivotal international Phase 3 trials, run by the US-based Multidisciplinary Association for Psychedelic Studies (MAPS) and sponsored by its public benefit corporation arm Lykos Therapeutics.

In the first, published in 2021, 88% of participants with severe PTSD who received MDMA-assisted therapy showed clinically significant improvement, and 67% no longer met the diagnostic criteria for PTSD.

A second trial in 2023, involving participants with moderate-to-severe PTSD, found 71.2% of those treated with MDMA no longer met PTSD diagnostic criteria by the end of the study.

Despite those results, the US Food and Drug Administration rejected the therapy's approval in 2024, citing insufficient evidence of its safety and effectiveness.

Regulators raised concerns that participants who had taken MDMA before produced an expectancy bias, complicating the trial data.

New Zealand's Ministry of Health said the new treatment would be tightly controlled, combining MDMA with psychotherapy in a clinical setting rather than take-home doses.

"Treatment takes place in a controlled clinical setting under the care of an authorised psychiatrist and forms part of a comprehensive treatment plan," the ministry said, adding that patients must be aged 18 or older.

Friday, August 28, 2026

 

Dutch institute issues 'Red Alert' over potentially lethal Trump-shaped ecstasy pills

This undated photo provided by Trimbos Institute of Mental Health and Addiction shows pills that have a depiction of President Donald Trump on one side
Copyright AP Photo

By Gavin Blackburn
Published on

It's not the first time ecstasy pills in the form of Trump's head have appeared. In 2017, German police seized thousands of orange Trump-shaped tablets.

A Dutch drug addiction and mental health institute warned users on Friday about potentially lethal ecstasy pills shaped to look like the head of US President Donald Trump.

The Trimbos Institute said that several of the pills have been handed in recently at a network of centres that test drugs for users before they take them.

“Absolutely do not use these pills,” the institute warned.

It released a photo of the pills that have a depiction of Trump's head on one side and on the other side “NL” and “Trump” stamped into the surface either side of a vertical line.

One of the pills has a green face and another is yellow.

The institute warned in a “Red Alert” published on its website and social media that they contain a high concentration of a chemical called PMMA, or para-methoxymethamphetamine, that is similar to MDMA, the active ingredient in ecstasy pills.

However, PMMA is slower working than MDMA and that could lead users to take more because they think that the first pill didn't work, leading to a risk of overdosing, the institute said, adding that use of the pills “can lead to overheating with possibly deadly consequences.”

Spokesperson Anniek Groothuis said that the institute has no reported cases of serious illness or fatalities among people who may have used the drug.

“We do not know of any victims where PMMA was found in their blood,” she said.

Producing, selling and using ecstasy is illegal in the Netherlands, but it's widely used, particularly at clubs and music festivals.

A government report in 2024 said that some 550,000 people took the drug in a year.

It's not the first time ecstasy pills in the form of Trump’s head have appeared. In 2017, German police seized thousands of orange Trump-shaped tablets.

Thursday, August 20, 2026

 

Study finds sustained benefit for people using Oregon psilocybin services



OHSU-led research is the largest study of psychedelics outside clinical trials




Oregon Health & Science University





People participating in an Oregon Health & Science University-led study of state-regulated psilocybin services reported relief from symptoms of anxiety, depression and post-traumatic stress disorder — with almost two-thirds declaring the experience to be among the most meaningful of their life.

The findings, published today in the journal JAMA Network Open, represent the first multisite study of the legalized psilocybin market approved by Oregon voters in 2020.

“Safety was very similar to what we’ve seen with psychedelics in clinical settings,” said lead author Todd Korthuis, M.D., professor of medicine (general internal medicine and geriatrics) in the OHSU School of Medicine. “That’s important because there was a big question around whether or not safety in carefully controlled psilocybin clinical trials would translate into real-world use.”

Oregon voters approved a non-medical wellness model, making state-licensed access to mind-altering “magic mushrooms” available for people aged 21 and older starting in 2023.

Senior co-author Adrianne R. Wilson-Poe, Ph.D., a scientist at the Legacy Research Institute and, with Korthuis, co-director of the Oregon Psychedelic Evaluation Nexis, noted that participants reported lasting benefits with few adverse events.

“This paper is going to be cited for decades,” she said. “This is the first large-scale study to monitor the safety and mental health symptoms of real people in the real world.”

The study enlisted 346 people who joined licensed facilitators for a single session using psilocybin between November 2024 and June 2026. Participants reported their state of mind at baseline, one week, one month and three months after single psilocybin sessions at 24 licensed service centers in Oregon.

Participants reported their experience through a web-based portal, with 90% continuing to do so through three months. Key findings:

  • At one month, 91.5% felt they benefited and 64.9% ranked the experience among the 10 most meaningful of their life.
  • At three months, participants reported decreased moderate-to-severe symptoms of depression, anxiety and PTSD. They also reported improved mental wellbeing and life satisfaction.
  • Few reported their experience as harmful, although four who used psilocybin for the first time experienced adverse behavioral reactions that required medical attention. No participants reported a serious event related to their physical health.

The findings will be presented today as part of a Psychedelic Innovation Summit in Portland co-hosted by OHSU and the Healing Advocacy Fund.

“These early results reveal psilocybin’s potential to improve health in people accessing these services here in Oregon,” said OHSU President Shereef Elnahal, M.D., M.B.A., who previously served as undersecretary of health in the U.S. Department of Veterans Affairs.  “The study also provides important insight for policymakers considering programs that permit psychedelics for the treatment of mental health conditions, including PTSD and substance use disorders affecting America’s military Veterans.”

High safety profile

Korthuis noted that psilocybin isn’t appropriate for people with psychosis, bipolar disorder or who are pregnant. However, he was struck by the low incidence of adverse events among participants in the study. Only seven participants reported the experience as harmful three months after their use of psilocybin.

“This may be a reflection of clients who were healthier overall than clinical trial participants,” Korthuis said. “The results demonstrate it’s safe for people receiving state-regulated psilocybin experiences.”

In contrast to previous clinical studies examining safety and effectiveness in treating moderate to severe depression, only about half of the Oregon study participants reported symptoms of moderate to severe depression beforehand. Even so, most participants reported improvements in their mental health, wellness and life satisfaction following their psilocybin session.

“Just because something isn’t a medical model doesn’t mean you can’t have mental health benefits,” Korthuis said. “Still, people serious mental health or medical conditions should talk with their healthcare providers before seeking services.”

Previous research, including imaging of the brain, indicates physiological changes that may help people to reset how they process information and view themselves, he said. More than 20,000 people have accessed Oregon licensed psilocybin services to date, seeking improved general health and wellness along with the potential of changing their perspective, according to data tracked by the Oregon Health Authority.

A $3.3 million, five-year federal grant awarded earlier this year will enable OHSU researchers to specifically examine psilocybin’s effect on people seeking state psilocybin services to reduce use of illicit substances. 

Wilson-Poe said the survey platform developed through this research initiative approved by OHSU’s Institutional Review Board can be easily adapted to measure outcomes from other forms of psychedelics even beyond Oregon — especially as other states consider policies to expand access. OPEN has already expanded to Colorado, the second state to approve regulated psilocybin services.

“It can give us an apples-to-apples comparison,” she said.

In Oregon, a major barrier to access is the cost, which ranges from hundreds to thousands of dollars for a session involving a state-licensed facilitator. In addition, several counties have opted not to permit psilocybin service centers at least in part due to concerns about the safety of psychedelics, whether they’re used medicinally or recreationally.

“Those counties may find this data reassuring, as may policymakers considering similar measures in other states,” Korthuis said.

In addition to Korthuis and Wilson-Poe, co-authors include Ryan Cook, Ph.D., Devin Gregoire, M.S., Kelli Pertl, M.P.H., Dennis McCarty, Ph.D., Ximena A. Levander, M.D., and Kim A. Hoffman, Ph.D., of OHSU; Christopher S. Stauffer, M.D., of OHSU and the VA Portland Health Care System; Jason B. Luoma, Ph.D., of the Portland Institute for Psychedelic Science; and Don Des Jarlais, Ph.D., of New York University.

The research was supported by the Substance Abuse and Mental Health Services Administration of the U.S. Department of Health and Human Services, grant award 75S20123P00003; the OHSU Foundation; the National Institute on Drug Abuse of the National Institutes of Health, grant awards R01DA060253, K12DA061526 and K01DA055130; and the Oregon Clinical and Translational Research Institute of OHSU through grant award UL1TR002369 through the National Center for Advancing Translational Sciences of the NIH. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health or the U.S. Department of Health and Human Services.

Saturday, August 01, 2026

Cameco Announces IPO Plan For Westinghouse


The plan is for Vogtle 3 and 4 to be joined by many more AP1000s in the US (Image: Westinghouse)

August 1, 2026
World Nuclear News


Key Takeaways:

Westinghouse Electric Company, jointly owned by Cameco and Brookfield, has confidentially filed for an initial public offering of its common stock, though share numbers and pricing remain undetermined.

The company reports a strong global pipeline of 91 potential AP1000 reactors totaling about 105 GWe, spanning the US, Europe, Canada, India, Saudi Arabia and other markets, with deployment windows from the mid-2030s onward.

Cost and construction timelines are projected to improve significantly with repeated builds: overnight capital costs could fall from $20–26 billion per near-term unit to $14–17 billion for “Nth-of-a-kind” projects, while build times shorten by 20–30%.


Westinghouse Electric Company, which is owned jointly by Cameco and Brookfield Renewable Partners, has confidentially submitted a draft registration statement relating to a proposed initial public offering of its common stock.

Announcing the registration ahead of its quarterly results call, Cameco said the number of shares to be offered and the price range for the proposed stock market offering have not yet been determined, and said the proposed offering would be subject to market and other conditions.

Westinghouse, which supplied the world’s first commercial pressurised water reactor (PWR) in 1957 in Shippingport, Pennsylvania, is one of the world’s largest nuclear services businesses. A strategic partnership of Cameco Corporation and Brookfield Renewable Partners acquired the company for a total enterprise value of approximately USD8 billion in a transaction completed in 2023: Westinghouse had previously been acquired out of bankruptcy by Brookfield Business Partners in 2018. Currently, Cameco owns a 49% interest and Brookfield owns the remaining 51%.

Speaking during Cameco’s results call, CEO Tim Gitzel said the company was “extremely limited” in what it could say under US Securities and Exchange Commission rules about the initial public offering (IPO). Nevertheless, the Westinghouse business segment featured heavily in Cameco’s quarterly results call, and its management’s discussion and analysis (MDMA) document for the quarter which ended on 30 June.

Westinghouse’s technology platform operates across the nuclear power value chain, Cameco said in its quarterly update, with 57% of the global operating fleet of 417 reactors using its technology, making it “one of the most strategically important franchises in the global nuclear power industry” with “growing global opportunities for its technologies”.

The MDMA documents a pipeline of deployment opportunities for 91 potential AP1000 reactors totalling some 105GWe across its global markets. These include: up to 10 units supported through American Nuclear Supply Chain Loans announced by the US Department of Energy earlier this year, with a commercial operation timeframe by the mid-2030s; up to 10 further US units supported through the strategic partnership between Cameco, Brookfield and the US Department of Commerce announced in 2025, for commercial operation by the mid-to-late 2030s; the resumption of the two-unit VC Summer project, for commercial operation by the early-mid 2030s; three units at Lubiatowo-Kopalino in Poland, for operation in the mid-2030s; two units each in Bulgaria (Kozloduy units 7 and 8) and Ukraine (Khmelnitsky units 5 and 6), for commercial operation by the mid-to-late 2030s; 11 units described as “FEED-Stage Projects” (FEED is front-end engineering and design) in the Netherlands, Slovenia, Finland/Sweden, and the USA, with a late-2030s timeframe; and up to 51 units in Canada, India, Saudi Arabia, Slovakia, the USA, and “other European countries”, with a deployment timeframe of late 2030s-early 2040s.

This list is ordered in terms of how close those opportunities are to final investment decisions, said Dominic Kieran, Global Managing Director of Cameco UK who is also the chair of Westinghouse’s Board of Directors. For those countries and projects further down the list, “it’s not that we see them as lower probability, it’s just that we see them as slightly earlier in the process of getting to final investment decision”, said Kiearn. For a “couple” of those, “we are seeing very, very strong recognition of need for nuclear in baseload energy generation”, he added.

Economic benefits

The MDMA includes illustrative economics for reactors deployed in the near term versus so-called Nth-of-a-kind deployments – that is, after five deployments of two reactor units located on a single project site for a total of 10 units, and a sustained demand of at least two reactor units per year, is achieved.

The nuclear construction period – from first nuclear concrete to commercial operation – is estimated as around 66 months per unit for near-term deployments, reducing by 20-30% for Nth-of-a-kind deployments. Meanwhile, the overnight capital costs decrease from USD20-26 billion for near-term deployments to USD14-17 for Nth-of-a-kind.

With a complete reactor design – AP1000s are in operation, Westinghouse is well positioned for the procurement aspects of new projects, and few bottlenecks are perceived around construction, Kieran said, adding that while, “certainly not without risks” the company has been “prudent” in its assessment.

Cameco President and Chief Operating Officer Grant Isaac spoke to the significance of the US government funding, including the importance of securing long-lead items to support construction projects. A standardised design, sequential construction projects, and “simplifying” projects – not by changing designs but by incorporating lessons learned – is the key to get to Nth-of-a-kind as quickly as possible, he added. “Nobody needs to fear nuclear new build – in fact, we need to embrace it,” he said.



About World Nuclear News

World Nuclear News is an online service dedicated to covering developments related to nuclear power. Established in 2007, WNN has grown rapidly to welcome over 40,000 individual readers to the website each month, while its free daily and weekly emails both reach more than 16,000 people. These figures represent a broad audience that includes not only nuclear professionals but also journalists, researchers, opinion leaders, policy-makers, and the general public.
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Friday, May 22, 2026

 

With AUKUS Risks and Aging Fleet, Australia Eyes Japanese Subs as Backup

Collins-class submarine HMAS Rankin: Yuri Ramsey/Department of Defence.
Collins-class submarine HMAS Rankin: Yuri Ramsey/Department of Defence.

Published May 21, 2026 3:32 PM by The Strategist

 

[By Richard Gray]

The reduced Collins-class submarine Life-of-Type Extension (LOTE) program, announced on 19 May, will cost more than previously expected and deliver less capability. The government’s decision to cut back the scope of the work also increases the risk to Australia’s possession of a modern, crewed submarine capability in the next decade.

AUKUS remains the best partnership for Australia to acquire the nuclear-propelled submarines necessary for Australia to manage the most dangerous era since World War II. But the now elevated risk of losing adequate conventional submarine capability in the meantime strengthens the case for preparing a Japanese fallback option.

Canberra should approach Tokyo to see how it could buy or lease Japanese submarines should they be required in the 2030s.

The Collins-class LOTE program as originally planned was always highly risky, so cutting back what will be done to the six submarines to keep them going is an understandable and responsible move. Instead of a more extensive LOTE, equipment on the submarines will be repaired and replaced as judged necessary for each boat. Sensors and weapons will be replaced where possible. The focus will be on maintenance and safety rather than enhanced capability. Replacement of the diesel engines and generators will be done only if judged to be critical.

The cost of the reduced LOTE is estimated at around A$11 billion, double what had been estimated for the full LOTE. This is likely not just because the previous costs were probably greatly underestimated but also because old equipment on the submarines will be increasingly expensive to maintain. Critical elements such as the hulls and in some cases the propulsion systems will be approaching or possibly exceeding 40 years of service by the end of the next decade, increasing the risks to safety and likely requiring intensive monitoring and maintenance.

This raises the question of value for money. Even if all goes according to the new plan, Australia will pay around A$1.8 billion per boat to keep roughly its current level of conventional submarine capability, at best. In all capability aspects this does not compare favourably with new, modern conventional submarines. For example, Japan’s Taigei?class submarines cost about A$600 million to A$700 million each. If further reductions to the scope of the LOTE occur – and the announcement yesterday leaves this prospect open, pending further engineering studies – a future government might decide that the running cost of an increasingly fragile and shrinking capability is not worth it and cut its losses. This could mean rapid retirement of older Collins-class vessels and even deciding not to extend the lives of some units, leaving a smaller and rapidly ageing submarine force until the arrival of nuclear boats.

The government plans that at any time three Collinses will be in deep maintenance, which will include life-extension work. Two of the remaining three are to be available for operations. Even assuming this can be achieved in what’s still likely to be a risky and technically challenging program, the life-extended submarines will possibly be less stealthy and probably have less endurance than previously planned. They will progressively fall behind newer regional competitors and probably be less able to undertake the full suite of required missions.

The reduction in planned submarine capability as a result of the de-scoped LOTE program increases the importance of achieving the remaining two key steps of the AUKUS Optimal Pathway, delivery to the Royal Australian Navy of US Virginia-class nuclear attack submarines (SSNs) and local construction of the follow-on Anglo-Australian SSN-AUKUS class.

The Virginias are due to arrive in the early 2030s, almost certainly not before 2032. But there is a significant risk that deliveries could be delayed – or even withheld if the US judges that it has too few SSNs for its own requirements. Since the Collins class is losing its competitiveness with age, delays to the Virginias and SSN-AUKUS could leave Australia without a modern crewed submarine capability for a decade or more – hence the need to get ready now for the Japanese fallback option.

As the ASPI report Hedging our Bets recommends, it is more than prudent to prepare now for the future contingency of rapidly buying or leasing conventional submarines from Japan (or even another partner) should these risks to Australia’s submarine capability emerge. The reduction in the LOTE program and resulting reduction in planned capability is a clear reminder that such risks are very real.

Richard Gray is a resident senior fellow at ASPI.

The opinions expressed herein are the author's and not necessarily those of The Maritime Executive.


Australia ‘disappointed’ by Chinese owner’s resistance to forced port sale



By AFP
May 21, 2026


Private Chinese company Landbridge acquired a 99 year lease to Darwin Port in 2015, prompting criticism of Australia from then-US President Barack Obama 
- Copyright AFP Jung Yeon-je

Australia’s defence minister Richard Marles said Thursday that Canberra was “disappointed” the Chinese leaseholder of the strategic Darwin Port was challenging efforts to return it to local ownership.

Private Chinese company Landbridge acquired a 99 year lease to Darwin Port in 2015, prompting criticism of Australia from then-US president Barack Obama.


Prime Minister Anthony Albanese pledged last year to return the northern port — which sits across the harbour from a defence base hosting 2,000 US Marines annually and tarmacs upgraded for US bomber aircraft — to Australian ownership.

In April, Landbridge’s billionaire owner Ye Cheng lodged a complaint in the World Bank’s tribunal for investment disputes, alleging Australia’s push for the company to sell the port had breached its free trade agreement with China and was taking a discriminatory approach.

“We’re committed to putting the Port of Darwin back into Australian hands,” Marles told reporters Thursday on a visit to Darwin.

“We’re disappointed about the steps that have been taken to put this toward the place of an international tribunal. Obviously, we will do everything in our power to defend that matter,” he said.

Marles also noted the US military was committed to “doing more from Darwin”.

Darwin is Australia’s closest port to Asia, and cargo shipments of commodities including iron ore and liquefied natural gas to China have dominated trade ties.

In January, China’s ambassador to Australia Xiao Qian warned if Landbridge were forced to leave the port it could impact wider trade and investment between China and Australia.


Australian Police Intercept a Diesel Generator Filled With Multiple Drugs

Drug packages within an apparent cylinder bore (AFP)
Drug packages encapsulated within an apparent cylinder liner, post-disassembly (AFP)

Published May 21, 2026 9:32 PM by The Maritime Executive


The Australian Federal Police are calling on diesel repair specialists to help with a rare technical problem: the agency has confiscated a used diesel generator that someone packed full with nearly every kind of illegal stimulant on the market, and it needs to find the people responsible for the shipment.

Early this year, Australian Border Force inspectors at Port Botany were conducting routine X-ray inspections of imported cargoes when they noticed something off about a heavy-duty diesel generator, which had arrived from Mexico by way of Malaysia. 

This generator was special: it appeared to have packages inside. The ABF contacted the AFP, who brought in specialists to have a closer look. Over the course of three days, they disassembled the generator and found a total of about 370 kilos of drugs inside; photos suggest the consignment was stashed in a cylinder bore.

Unusually, the shipment was very diverse. Large-scale imports typically have just one or two drug classes, but this one had about 120 kilos of cocaine, 250 kilos of methamphetamine, three kilos of MDMA and 800 grams of 2CB ("pink cocaine"), a lab-made club drug with stimulant and psychedelic effects.  

"This mixed bag of illicit drugs was likely destined for several different criminal groups, to be sold into a range of communities. Despite the elaborate attempt to conceal such a large quantity of drugs, the coordinated efforts of law enforcement ensured these substances never reached Australian streets," said Detective Acting Superintendent Stuart Kimbell in a statement. 

Kimbell said that the AFP is looking for tips from the public - particularly from anyone who might have been approached about storage space for a generator, or spare parts vendors or diesel engine technicians who may have fielded inquiries about repairs. (The make and model of the engine were not released.)

According to ABF, this intercept ranked high on the list for technical complexity and detection difficulty. "ABF officers are highly skilled at identifying anomalies across all forms of incoming cargo, no matter how elaborate the concealment," said ABF Superintendent Jared Leighton.

Separately, the AFP announced that it had busted the alleged ringleader of an insider smuggling network at Port Botany. The 29-year-old suspect stands accused of organizing multiple drug pickup attempts at the port, including a 500-kilo shipment last year. The organizer allegedly paid a competitive wage to entice co-conspirators, up to US$140,000 per person per pickup - nearly three years of earnings for a typical Australian worker. 

Australia is the world's leading per-capita consumer market for cocaine and methamphetamine, and import prices are accordingly high. While wholesale prices fluctuate with availability, cocaine typically attracts more than US$100,000 per kilo on the Australian market. 

Wednesday, May 20, 2026


‘Profound Disappointment’: Democratic Virginia Gov. Spanberger Vetoes Legal Cannabis Sales

“The governor’s decision leaves the commonwealth exactly where we have been since 2021: with an unchecked illicit market hurting our communities, harming our youth, and putting adults at risk,” said one critic.


Then-Congresswoman Abigail Spanberger (D-Va.) speaks during a press conference in Fredericksburg, Virginia on November 3, 2022.
(Photo by Samuel Corum/Getty Images)


Brett Wilkins
May 19, 2026
COMMON DREAMS

Criminal justice reform and cannabis legalization advocates led condemnation of Democratic Virginia Gov. Abigail Spanberger’s Tuesday veto of legislation that would have established a retail market for the sale of recreational-use marijuana, which has been legal in the state for five years.

In 2021, Virginia became the then-16th state to pass an adult-use marijuana legalization law, with sales set to begin in 2024. However, former Republican Gov. Glenn Youngkin repeatedly vetoed the legislation, which would establish the framework for regulating and taxing the plant’s recreational use.

Today, while adults can legally consume cannabis recreationally, cannabis sales in Virginia are still restricted to medical use, and patients must travel to one of the five licensed providers in the commonwealth.

In March, Virginia lawmakers passed a package of bills to legalize recreational cannabis sales to people age 21 and older via a regulated market, place oversight of such sales under the Virginia Cannabis Control Authority, increase the public possession limit from one ounce to 2.5 ounces, allow delivery sales, establish new state and local cannabis taxes, and set January 1, 2027 as the launch date for sales.

Spanberger—who had campaigned on a promise to sign legislation establishing recreational cannabis sales—proposed amendments to the bill that were rejected by the General Assembly.

“I support the intent of many of the bills I am vetoing,” she explained in a statement. “However, it is my responsibility as governor to make sure all new laws can be successfully implemented and protect against unintended consequences that harm Virginians.”

“I look forward to continuing to work with bill patrons, state and local leaders, and advocates on legislation addressing these issues in the future,” the governor said.

Marijuana Moment reported that Spangberger sought to delay the start of sales by six months, increase taxes, and institute new criminal penalties for cannabis consumers.

“Once again, Virginia’s efforts to establish a safe, regulated, and equitable adult-use cannabis marketplace has been halted despite years of work, public input, and broad recognition that the status quo is failing Virginians,” state Sen. Lashrecse Aird (D-63), who sponsored one of the bills, said in a statement Tuesday.

“The governor’s decision leaves the commonwealth exactly where we have been since 2021: with an unchecked illicit market hurting our communities, harming our youth, and putting adults at risk,” she added.

Del. Paul Krizek (D-16), who sponsored the House of Delegates version of the sales bill, said, “Five years ago, Virginia legalized cannabis in recognition that the War on Drugs has caused disproportionate harm to Black families and communities.”

“The question now is whether Virginia will continue allowing an unregulated illegal market to thrive, or finally establish a safe, transparent system that protects consumers, keeps products away from children, and keeps our commitment to ending racially discriminatory marijuana policing in Virginia,” he added.

JM Pedini, development director for the advocacy group National Organization for the Reform of Marijuana Laws and executive director for Virginia NORML, told Marijuana Moment that Spanberger’s veto is “a profound disappointment to the many Virginia voters who believed her when she said on the campaign trail that she supported establishing a regulated adult-use cannabis market.”

“It is also a slap in the face to the years of serious work undertaken by lawmakers, policy experts, advocates, public health stakeholders, and regulators who spent more than half a decade researching, debating, and carefully crafting this legislation,” Pedini added. “Rather than build upon that work, the governor dismissed it in favor of out-of-touch proposals to recriminalize cannabis consumers that lawmakers rightly rejected.”



Chelsea Higgs Wise, executive director of the Richmond-based nonprofit Marijuana Justice, said in a statement that “for five years, Virginia has been stuck in a limbo where adults can legally possess, share, and grow cannabis, but there is still no regulated way to purchase it.”

“By rejecting the retail bill,” Wise added, “the governor has chosen to extend that chaos rather than move us toward a transparent, accountable retail system that centers public health, public safety, and justice.”

Twenty-four states have legalized recreational marijuana, while 16 states allow medical use of the plant. Last month, the US Department of Justice began reclassifying cannabis from Schedule I—a category that includes dangerous drugs like heroin, LSD, and MDMA to Schedule III, which includes codeine, ketamine, anabolic steroids, and testosterone.

Sunday, May 17, 2026

 

Trip to recovery: How psychedelics could revolutionise mental health care

Psychedelic-assisted therapies have shown promise in treating the cognitive ruts of several mental health conditions.
Copyright Canva

By Amber Louise Bryce
Published on


In a world gripped by a growing mental health crisis, research suggests that psychedelic-assisted therapy could be an answer. Euronews Health spoke to an expert about how they work, and when - if ever - we might see them approved.

Picture this: You walk into a small, dimly lit room and lay on a bed beside a clinician. After talking you through what’s going to happen, they hand you an eye mask, then administer a controlled dose of the psychedelic compound, psilocybin.

As suddenly as the drug takes effect, the world as you knew it starts to dissolve - the chains of old thought patterns finally loosen.

While it might sound intense, this scenario could be a future reality for those living with treatment resistant mental illness, including depression and post traumatic stress disorder (PTSD).

In recent years, psychedelic-assisted therapies have become one of the most fascinating and fast-accelerating areas of psychiatric research, driven by an ever-growing body of exciting new evidence.

The current mental health crisis has also created an urgency for new, more effective treatment options, with over a billion people currently living with mental health disorders, according to the World Health Organization (WHO).

“Unfortunately, in mental health, and specifically in psychiatry, we haven't really had any new treatments for several decades,” Dr Liliana Galindo, an assistant professor at the University of Cambridge’s psychiatry department, told Euronews Health.

“What psychedelics are bringing is the opportunity to have or to present new treatments for people that don't respond to the usual treatments.”

Psychedelics are a class of psychoactive substances that can powerfully alter people's perceptions and moods by binding to serotonin receptors. Popular examples include psilocybin, DMT, phenethylamines (MDMA) and lysergamides (LSD).

While they all share similar consciousness-expanding qualities, each compound varies in its intensity, duration, and overall effect, with different ones being tested for different conditions.

So far, psilocybin, an active ingredient in magic mushrooms, has generated the most promising results.

“For treating depression, psilocybin, specifically the COMP360 (a synthetic formulation of psilocybin developed by Compass Pathways), has already finished phase three of its clinical trials. We are expecting that [Compass] is going to file the FDA (Food and Drug Administration) application soon,” Galindo said.

“Potentially, this could be the very first psychedelic treatment that will be legal and approved.”

How do psychedelic-assisted therapies work?

Up until now, mental health treatments have relied on two evidence-based methods: talk therapies and medications such as antidepressants.

These are proven to be effective, with patients receiving a combination of the two 25-27% more likely to respond positively, according to statistics by the National Institutes of Health.

But for those that don’t respond, other avenues of help remain limited.

“Many mental health conditions have some symptoms that are common, like rigid cognitions. So, for example, when people are depressed, they start to have really negative thoughts, and these negative thoughts are going to affect how they see themselves, how they see the world, and of course, how they are going to feel about it. And after several years of being depressed, it's really difficult to take a step outside of those pessimistic thoughts, or frequent fears and even suicidal ideations,” Galindo explained.

For these cases, psychedelic medications could be the answer, with Galindo noting their effectiveness at disrupting cognitive ruts and rewiring how the brain processes trauma.

“I really like an analogy I saw once [about psychedelic medications] that it's like when you're skiing. You usually go for a certain pathway, right? And because the pathway has a specific mark, it is really difficult to actually go outside of it. But somehow, what psilocybin allows, is like having fresh snow that will make it easier to actually explore different pathways.”

Numerous studies back this, with a recent one by Imperial College London - considered a world leader in psychedelic research - reporting that even a single dose of psilocybin can prompt anatomical changes in the brain.

Other psychoactive compounds such as MDMA have been shown to work a little differently by enhancing feelings of empathy, connectivity and openness, which could be effective at treating PTSD.

“It facilitates a period of time where people [with PTSD] can revisit their memories and somehow be able to rethink, to reframe, to change the narrative and to process their trauma,” she said.

“This is the reason psychedelics are bringing such a big revolution to mental health, because they're aiming to treat the core rather than only the symptoms.”

Social stigmas and legal issues

A major hurdle to mainstream approval, however, remains their status as illegal drugs in most countries.

“Unfortunately, even if we have clear evidence for their therapeutic potential, they are still illegal. For example, here in the UK, they're still classified A, meaning that in order to conduct any study, we need to apply for a special home office licence. This is not only expensive, but takes a long time, and so is definitely affecting the amount of research that could be happening in the field,” Galindo said.

Another issue is the stigmas surrounding these drugs, and their primary associations with party culture and potentially dangerous outcomes.

Galindo emphasises that these concerns are why the controlled setting of psychedelic-assisted therapies is so important.

“You need to take care of all the different details of the environment, like the sound, the lights. And of course, the entire time [the patient] is supported by a trained therapist or a member of the staff that is there to be able to support during that process,” she said.

“These drugs are really powerful tools, but of course, if for any reason they are not given in the right setting, this could come with more side effects.”

While more research is required to better understand who will benefit and who won’t, Galindo hopes that, one day, these treatments can become an accessible option for everyone.

“Rather than staying in a private setting, they should be available for the people who need it the most, not only for the ones that can pay.”