Relax rules on research into illegal drugs, say advisers

Independent government advisers have called for rule changes to allow more research into therapeutic uses of illegal drugs, including psychedelics.

The Advisory Council on the Misuse of Drugs (ACMD) proposes easing controls on trials using Schedule 1 drugs – which include opium and LSD.

Recent studies have found psychedelics could help treat severe depression.

MP Charlotte Nichols said further research could lead to “transformative mental health treatments”.

Ms Nichols has previously spoken in Parliament about a need for research into the potential medicinal uses of hallucinogenic mushrooms to treat her PTSD.

The Labour MP described her condition as “living hell”.

Ms Nichols, who chairs the Centre for Evidence Based Drug Policy (CEBDP) forum, said the report was “an important milestone on the road” towards better treatment.

“We have high hopes that the government will now urgently work to break down barriers to research into LSD, psilocybin, MDMA and other drugs with the potential to be transformative treatments for anxiety, severe depression and PTSD,” she said.

There have been recent successes in using a drug based on a compound in hallucinogenic mushrooms to improve the symptoms of severe depression.

Psilocybin appeared to free up the brains of people with severe depression in a way that other antidepressants did not.

‘Right balance’

The ACMD found the process of applying for a licence to use Schedule 1 drugs like psilocybin in scientific trials could take a year.

Tough rules and extensive paperwork mean only major, well-funded studies can carry out clinical trials.

If granted, licences are valid only for three months – which is often insufficient for organising shipments of drugs and managing paperwork.

Relaxing these rules would open up research, allowing more academic and medical studies, the ACMD said.

The Home Office will now consider the report and respond in the new year. It has been approached for comment.

Chris Philp, the Home Office minister responsible for drug policy, has previously said “ensuring that the UK is a world-leading jurisdiction for pharmaceutical, clinical and other medical research is a top government priority”.

But, in a letter to the ACMD before the report was published, Mr Philp said the government must “maintain the right balance between access for legitimate research whilst minimising the risk of harm, diversion, and misuse of controlled drugs.”

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