Post-traumatic stress disorder, known as PTSD, is high unmet needs in neuropsychiatric disorders. As victims of trauma, PTSD patients are coerced by their dysregulated brain chemistries to relive their traumatic experiences, where specific triggers provoke fearful symptoms such as flashbacks, intrusive thoughts, nightmares and severe anxiety. Unfortunately, current drugs for PTSD address only specific symptoms and are highly ineffective, with 70% of the over 15 million people suffering from PTSD that are not adequately cured, and instead are at risk of developing substance abuse disorders and committing suicide. The endocannabinoid system is a neural circuit that is highly dysfunctional in PTSD patients, and new drugs that modulate this circuit in a safe and sustainable manner have the potential to be the first effective treatment for PTSD.
Tourette Syndrome is another indication in which deviations in the endocannabinoid system appears to play an important role. The disease affects a lot less patients than PTSD (400,000 in the EU and US), but patients are similarly affected by a lack of effective treatments that reduce symptoms without severely affecting their quality of life.
In this feasibility study, the overall objective was to assess market, clinical and preclinical feasibility of first-in-class endocannabinoid modulators for PTSD and Tourette’s, and to update Synendos’ business plan with results of the study.