The DEA Wants Five More Tryptamines in Schedule I. Comments Close October 23
A proposed rule would place five tryptamines into Schedule I. It is the second attempt at the same action, and comments close October 23.
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A proposed rule would place five tryptamines into Schedule I. It is the second attempt at the same action, and comments close October 23.
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Israeli MDMA trials run 15 sessions over three to four months, including an eight hour dosing day with two therapists present. The staffing math is the part US clinics should be reading.
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A new letter in npj Mental Health Research argues a 2024 meta-analysis compared ketamine and psilocybin with different instruments. Across the same ketamine studies, one scale explains 3 percent of outcomes and another explains 15 percent.
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Higher dissociation scores went with better depression outcomes on subcutaneous esketamine, with derealization driving the difference. The study was small, open label and exploratory.
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From FDA's October 5 psychedelics docket to the DEA telehealth expiration and Medicare's 2027 in-person rule, six dates every ketamine clinic should plan around.
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Oxford found ketamine quieted the habenula 24 hours after infusion. A Texas A&M analysis linked 24-hour brain changes in older veterans to day-7 improvement.
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Definium's DT120 met its primary endpoint in the Panorama trial. A low-dose arm was added to address functional unblinding, and a dose-response pattern emerged.
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FDA heard four hours of testimony on psychedelic approval and asked no questions. The real contest was over label language, which decides who can deliver these drugs.
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A Center for Health Care Strategies report examines how psychedelic-assisted therapy could reach Medicaid. Some states already cover off-label IV ketamine.
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A systematic review screened 897 references on psilocybin microdosing. Of 11 studies, only two were placebo controlled, and neither found a benefit.
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