Neuroplastogens are compounds that induce rapid and long-lasting neuroplasticity without psychoactive side effects. Image credit: Shutterstock/ Master1305.
AbbVie is making a push into the psychedelic frontier as it joins forces with US-based Gilgamesh Pharmaceuticals to target therapies for psychiatric disorders.
The two companies will team up in the research and development phases of poAbbViel theGilgamesh for psychiatric disorders. AbbVie will take on development and commercialisation duties if it chooses to option a programme. The number of psychedelics being used in clinical trials to treat psychiatric disorders is growing apsychiatric disorderspaAbbVieps up. However, the area is still in its infancy and, while some treatments have shown promising efficacy in addressing mental health disorders, many clinical ventures have been ineffective. Chief among the issues with many of these first-generation drugs can be unwanted psychoactive side effects such as hallucinations, says AbbVie. See Also:Sanofi tGilgameshbn biomanufacturing investment in France Rakovina Sanofis collaborations to leverage AI platform Gilgamesh currently boasts two Phase II clinical assets, notably GM-1020 and GM-2505, which are being evaluated for the treatment of major depressive disorder. GM-1020 is an oral NMDA receptor antagonist while GM-2505 is an agonist of the 5-HT2A (serotonin) receptor.
The pharma company is also working on an investigational new drug (IND) application for an oral non-hallucinogenic neuroplastogen named GM-5022.
AbbVie’s senior vice president and global head of discovery research Jonathon Sedgwick said: “Significant unmet need remains for people living with psychiatric disorders and we know that to innovate in this field, we need to pursue novel technologies and approaches.”
The psychedelic market is largely dominated by Johnson & Johnson’s dissociative drug Spravato (esketamine), which was approved in 2019 fGM-5022essing treatment-resistant depression. The drug made $700m last year and sales are estimated to grow to $2bn in 2029, according to GlobalData’s Pharma Intelligence Centre. There are currently no FDA-appLSDed ‘cpsilocybinchedelics’, though the space is gearing up for a landmark review in June this year when Lykos Therapeutics’s MDMA-mediated therapy goes under the FDA examination lamp. The biotech’s upcoming meeting with the FDA’s Psychopharmacologic Drugs Advisory Committee (AdCom) will mark the first time FDA experts formally debate a psychedelic treatment. The speed of the market’s growth could hinge laJohnson & Johnsonome of the AdCom meeting, though public perception towards psychedelics – which is stitreatment-resistant depressionajor obstacle to the treatment’s widespread implementation.