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The panel of advisers to the Food and Drug Administration sided against the overall benefits of MDMA when used to treat post-traumatic stress disorder. They cited flawed study data, questionable research conduct and significant drug risks, including the potential for heart problems, injury and abuse. The vote followed hours of pointed questions and criticisms about the research submitted on MDMA — sometimes called ecstasy or molly. Panelists pointed to flawed studies that could have skewed the results, missing follow-up data on patient outcomes and a lack of diversity among participants. The vast majority of patients studied were white, with only five Black patients receiving MDMA, raising questions about the generalizability of the results. The FDA advisers also drew attention to allegations of misconduct in the trials that have recently surfaced in news stories and a report by the nonprofit Institute for Clinical and Economic Review , which evaluates experimental drug treatments. The incidents include a report of apparent sexual misconduct by a therapist interacting with a patient. Lykos Therapeutics, the company behind the study, said it previously reported the incident to the FDA and regulators in Canada, where the therapist is based. The group was founded in to promote the benefits of MDMA and other mind-altering substances. When used to enhance talk therapy, the drug appears to help patients process their trauma and let go of disturbing thoughts and memories. But the panel struggled with the reliability of those results, given the difficulties of objectively testing psychedelic drugs. Because MDMA causes intense, psychological experiences, almost all patients in two key studies of the drug were able to guess whether they had received the MDMA or a dummy pill. Rajesh Narendran, a University of Pittsburgh psychiatrist who chaired the panel. Results were further marred by other complicating factors, including a large number of patients who had previously used MDMA or other psychedelics drugs recreationally. Nearly three dozen public speakers also addressed the panel, including veterans who said they benefitted from MDMA therapy, medical professionals who advised against its use and journalists and independent researchers who reiterated the allegations of misconduct in the trials. The AP is solely responsible for all content. June 4, No profanity, hate speech or personal attacks. No off-topic remarks. No disinformation about current events. We will remove any comments — or commenters — that do not follow this commenting policy. Send a letter to the editor.
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About a. Kevin Naugle said in a news release. Detectives found in the home a disassembled electric pill press with pink powder stuck to it, along with pills and a large plastic container with the same residue, a sifter and a scoop. They also located a spectrophotometer, which can be used to measure the purity and quality of substances. You can reach Staff Writer Madison Smalstig at madison. On X Twitter madi. Police: Press capable of making hundreds of pills per minute found in Santa Rosa home It is the first time such a device has been found locally, police said. July 24, This device is unable to display framed content. Click here to view this embed. No profanity, hate speech or personal attacks. No off-topic remarks. No disinformation about current events. We will remove any comments — or commenters — that do not follow this commenting policy. Send a letter to the editor.
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Panel rejects psychedelic drug MDMA as a PTSD treatment in possible setback for advocates
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