Cybin (NEO: CYBN) (NYSE American: CYBN), a clinical-stage biopharmaceutical company committed to revolutionizing mental healthcare by developing new and innovative next-generation psychedelic treatment options, is reporting on interim results from its phase 2 study of CYB003, the company’s proprietary deuterated psilocybin analog, designed to treat major depressive disorder (“MDD”). According to the announcement, the results demonstrate a rapid, robust and statistically significant reduction in symptoms of depression three weeks following a single 12mg dose compared to placebo. The phase 2 clinical trial is using the Montgomery-Asberg Depression Rating Scale (“MADRS”) scale to evaluate efficacy of the proprietary treatment. The company noted that dosing has been completed in all dose cohorts up to 16mg and that the study is showing a favorable safety and tolerability profile with no treatment-related serious adverse events observed.
“The overwhelmingly positive interim results for the 12mg dose of CYB003 are extremely encouraging for patients and providers,” said Cybin CEO Doug Drysdale in the press release. “The efficacy demonstrated at that dosage showed an unprecedented reduction in depressive symptoms compared to currently available treatments. With these encouraging results in hand, we look forward to sharing the full complement of topline data later this quarter, and 12-week durability data in the first quarter of 2024. Our planning continues as we prepare for a larger international, multisite Phase 3 trial in early 2024 to further evaluate the safety and efficacy of CYB003 in people suffering from MDD. . . . This is an exciting time — not only for Cybin, but for the entire psychedelics sector — as we now have interim results showing a significant improvement in depressive symptoms with a single dose, moving us ever closer to delivering on our mission to improve the treatment landscape across the spectrum of mental health disorders.”
To view the full press release, visit https://ibn.fm/ggxjM
About Cybin Inc.
Cybin is a clinical-stage biopharmaceutical company on a mission to create safe and effective psychedelic-based therapeutics to address the large unmet need for new and innovative treatment options for people who suffer from mental-health conditions. Cybin’s goal of revolutionizing mental healthcare is supported by a network of world-class partners and internationally recognized scientists aimed at progressing proprietary drug-discovery platforms, innovative drug-delivery systems, and novel formulation approaches and treatment regimens. The company is currently developing CYB003, a proprietary deuterated psilocybin analog for the treatment of major depressive disorder, and CYB004, a proprietary deuterated DMT molecule for generalized anxiety disorder; the company also has a research pipeline of investigational psychedelic-based compounds. Headquartered in Canada and founded in 2019, Cybin is operational in Canada, the United States, the United Kingdom, the Netherlands and Ireland. For more information, visit the company’s website at www.Cybin.com.
NOTE TO INVESTORS: The latest news and updates relating to CYBN are available in the company’s newsroom at https://ibn.fm/CYBN
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