Eagerly awaited results of the largest-ever study of psilocybin were announced Tuesday, with Compass Pathways revealing the psychedelic drug was highly efficacious as a therapy for treatment-resistant depression. Still, the company’s stock price had dropped more than 20% as of midday, perhaps because of safety concerns among investors.
The Phase 2b study is the largest randomized, controlled, double-blind trial of psilocybin, the psychedelic compound in magic mushrooms. The company said it found that patients who were given the highest dose, 25 milligrams, had a significant decrease in depressive symptoms compared to those given 1 milligram, which is such a low dose it functions as a placebo.
Overall, 29.1% of patients in the highest-dose group were in remission three weeks after treatment, compared to 7.6% of those in the control group, and more than a quarter of the patients in the 25-milligram arm were still in remission three months after treatment.
Those who received the highest dose also experienced an average reduction on a measure of clinical depression (the Montgomery-Asberg Depression Rating Scale) that was 6.6 points greater than those who took 1 milligram. Other patients were given a 10-milligram dose, but there was not a statistically significant impact for those patients compared with the 1-milligram arm.
“Everyone agrees such a result hasn’t been seen before in depression research, so we’re incredibly happy with that result,” said Lars Christian Wilde, co-founder and president of Compass.
Boris Heifets, a neuroscience researcher at Stanford who studies psychedelics and was not part of the study, agreed the results are “super promising.” The effectiveness of psilocybin at three weeks, according to Compass’ study, is roughly comparable to the effects of ketamine at one day, according to a smaller 2013 study, he added, which suggests the benefits of psilocybin hold up well over time. “We’re still missing a lot of the detailed data,” he added, but the summary results are “pretty good news.”
The study, which enrolled 233 patients at multiple sites across Europe and North America, is the most rigorous trial on psilocybin for treatment-resistant depression and adds considerable weight to earlier, smaller studies of the drug that were also promising. The U.S. Food and Drug Administration has granted Compass Pathways’ treatment breakthrough therapy designation, meaning the drug approval process will be accelerated if studies continue to show positive results. Compass is working toward starting a Phase 3 trial next year; current results suggest it’ll likely use a 25-milligram dose, but Wilde said that decision will be made following conversations with regulators.
The results released by the company, which have not been published in a medical journal or peer-reviewed, included side effects data showing a small number of serious adverse events. Overall, 12 patients reported treatment-emergent serious adverse events, five of whom were in the 25-milligram group and six in the 10-milligram group; these included suicidal behavior and self-injury. Just one patient in the 1-milligram group experienced a serious adverse event.
“The suicidal behaviors were reported at least one month after the administration of treatment and they occurred in patients who were essentially non-responding,” Guy Goodwin, Compass’ chief medical officer, said in an investor call Tuesday morning. In at least one case, though, suicidal ideation was reported early on in treatment, he added.
The numbers are small enough for the difference between treatment arms not to be statistically significant, said Wilde, noting that suicidal behaviors and ideation are common among depressed patients. “We’re dealing with a severe patient population, both in terms of patient severity and duration of their depressive episode,” he said. “Unfortunately, those events have to be expected.” There were three suicides in studies of esketamine, the only psychedelic currently approved for treatment-resistant depression, he pointed out.
Researchers in previous studies have reported a “disappointment reaction,” whereby patients’ symptoms worsen because the novel treatment doesn’t immediately cure their depression. The difference between the treatment arms is unexpected, said Heifets, as patients tend to get more depressed if they’re assigned to placebo and don’t get effective treatment: “If anything, I’d expect it to go the other way.” But, he added, suicidal behaviors are common in research on depressed patients. “That means it’s not attributable to psilocybin having a suicidal side effect,” he said.
Goodwin said the researchers plan to study the data in more detail, including analyzing responses to a questionnaire all patients took for suicidal assessment, to better understand the connection.
If you or someone you know is considering suicide, contact the National Suicide Prevention Lifeline at 1-800-273-8255 (Español: 1-888-628-9454; deaf and hard of hearing: 1-800-799-4889) or the Crisis Text Line by texting HOME to 741741.