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The company sponsoring the research said it plans later this year to seek US approval to market the drug, also known as ecstasy, as a PTSD treatment when combined with talk therapy.
“It’s the first innovation in PTSD treatment in more than two decades. And it’s significant because I think it will also open up other innovation,” said Amy Emerson, CEO of MAPS Public Benefit Corporation, the research sponsor.
Earlier this year, Australia became the first country to allow psychiatrists to prescribe MDMA and psilocybin, the psychoactive ingredient in psychedelic mushrooms. The drugs are gaining wider cultural acceptance in the US in part because of efforts by the nonprofit advocacy group Multidisciplinary Association for Psychedelic Studies.
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Common side effects in the MDMA group were muscle tightness, nausea, decreased appetite and sweating. But only one person in the MDMA group dropped out of the study.
After treatment, 86 per cent of the MDMA group improved on a standard PTSD assessment compared to 69 per cent of the placebo group. The assessment measures symptoms such as nightmares, flashbacks and insomnia.
By the study’s end, 72 per cent of people in the MDMA group no longer met the diagnostic criteria for PTSD, compared to about 48 per cent of the placebo group.
“The results that they got are very exciting,” said Barbara Rothbaum, who directs the Emory Healthcare Veterans Program in Atlanta. She was not involved in the research, which was published in the journal Nature Medicine.
PTSD also can be treated with other medications or talk therapy.
“They are very effective, but nothing is 100 per cent effective,” Rothbaum said. “So we absolutely need more options for treatment.” Before MDMA could be prescribed in the US, the Food and Drug Administration would need to approve it and the Drug Enforcement Administration would need to change its classification. MDMA is currently classified as Schedule 1, on par with heroin and deemed to have “no currently accepted medical use and a high potential for abuse”.