Doubledown. Psyence Biomedical Ltd accelerates its journey as a vertically integrated life science biotech company.
TWO phase IIb data readouts now anticipated in 2025. Also sharing news of the Psyence Biomedical Ltd expanded pipeline, the acquisition of Clairvoyant Therapeutics, subject to due diligence and customary closing conditions.
Our Phase IIb trial evaluating nature-derived psilocybin with psychotherapy as a potential treatment for Adjustment Disorder in a Palliative Care context in on track with iNGENū CRO, the FDA-centric Australian CRO, a partnership which grants us the economic benefits, including significant R&D tax credits.
At a time of increased regulatory scrutiny, we are happy to deepen our collaboration with Fluence a global leader in providing comprehensive, evidence-based psychedelic training to healthcare professionals and to achieving a therapeutic alliance that we hope will set a gold standard of excellence.
Together with our partners, Fluence and iNGENū CRO we look forward to topline data in the back half of next year that, if positive, will support the initiation of a pivotal Phase III trial for an indication --Adjustment Disorder-- which WHO deems 7th most diagnosed psychiatric condition in the world.
We have strengthened our Clinical Supply of Natural Psilocybin by partnering with Optimi through a non-binding Letter of Intent (LOI) whereby Optimi will be our exclusive supplier of GMP nature-derived psilocybin extract for both our Phase III trial (assuming the Phase IIb study is successful) as well as subsequent commercialization.
With Optimi's collaboration, we look to bring transformative treatments for mental health conditions, achieve pioneering advancements in psychedelic-based mental health therapies and enable Psyence Biomedical Ltd to help patients in Palliative Care context.
Second Indication: We also announced our second indication, and will evaluate GMP nature-derived psilocybin as a potential treatment for Substance Use Disorders (SUDs), including Alcohol Use Disorder (AUD). Our agreement with PsyLabs secures highly purified nature-derived psilocybin extract exclusively for these indications.
Acquisition of Second Phase IIb Asset
Deepening our commitment to helping relieve the human misery of AUD to diversify our drug development pipeline, we signed conditional agreement to acquire of psilocybin-based drug developer Clairvoyant Therapeutics.
Clairvoyant is currently executing a Phase IIb clinical trial in AUD, with topline data expected in early 2025. "We are pleased to join forces. . .with our 'speed to market' strategy for psilocybin in AUD'" said Damian Kettlewell Clairvoyant CEO.
Finally, to ensure that we have the critical funding required to advance these initiatives, we entered into agreements that are expected to provide us with sufficient capital to execute our strategy.
Proud to share more details in a letter from our CEO Dr. Neil Maresky, please see below.