MindMed Completes Phase 1 Clinical Trial Of Non-Hallucinogenic Proprietary Derivative Of Ibogaine




On Tuesday, Mind Medicine Inc. (NASDAQ:MNMD) (NEO: MMED) (DE: MMQ) reported the completion of its Phase 1 clinical trial of 18-MC, the company’s non-hallucinogenic proprietary derivative of ibogaine, being developed for the treatment of indications linked to opioid use disorder.

The New York-headquartered psychedelic-focused biotech company noted that the trial was completed in December 2021 with topline results expected in early 2022.

“This is an exciting milestone, and we look forward to announcing the results of our Phase 1 study in the coming months,” Robert Barrow, CEO and director of MindMed stated. “The growing opioid crisis claims over 75,000 lives each year and impacts more than we’ll ever know. While ibogaine has been used and studied as a treatment for opioid addiction, its efficacy, while promising, has been overshadowed by significant safety concerns. Our proprietary molecule, 18-MC, has indicated an encouraging safety profile and preclinical efficacy data setting the stage for our Phase 2a proof-of-concept study in individuals undergoing opioid withdrawal. We expect to initiate this study in early 2022, which will evaluate the safety, tolerability and efficacy of 18-MC in mitigating the symptoms of opioid withdrawal.”

The Trial Details

The reported Phase 1 single and multiple ascending dose trial, conducted at a clinical research site in Perth, Australia, examined the safety, tolerability, pharmacokinetics, and effects on the cognitive activity of 18-MC in healthy volunteers. 18-MC is a receptor antagonist that modulates excessive dopamine fluctuations in the mesolimbic system of the brain. It is a synthetic organic molecule around a coronaridine chemical backbone common to a number of plant-based medicinal compounds, including ibogaine.

Subjects either received doses between 4 and 325 milligrams twice per day (for one day; n=5 per arm) or doses between 2 and 90 milligrams twice per day (for up to 7 days, n=5 per arm).

In preclinical efficacy models, 18-MC has demonstrated strong activity in reducing both withdrawal symptoms and self-administration of opioids, stimulants and other substances of abuse.

Extensive preclinical characterization has shown 18-MC to have a strong safety and tolerability profile. Importantly, 18-MC has the potential to overcome the safety limitations of ibogaine and has not demonstrated proarrhythmic or neurotoxic activity.

More recent news from MindMed:

MindMed Advances Phase 2a LSD Microdose Trial For Adult ADHD

MindMed Shares Update On Phase 2b Trials of LSD For Treating Generalized Anxiety Disorder

EXCLUSIVE: MindMed CEO Rob Barrow On Growth Aspirations, Development Pipeline

Price Action

MindMed’s shares traded 0.66% lower at $1.51 per share during Tuesday’s pre-market session.

Photo: Courtesy of Jynto via Wikimedia Commons.





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