PharmAla, University of Calgary, and Heroic Hearts Canada to partner on a groundbreaking observational trial
VANCOUVER, BC, November 9, 2023 - PharmAla Biotech Holdings Inc. (“PharmAla”)(CSE: MDMA) (OTC:PMBHF), the University of Calgary (“UC”), and Heroic Hearts Canada (“HHC”, and collectively, the “Parties”) are pleased to announce that they have completed a Letter of Intent (“LOI”), and received initial Ethics Board Approval, to initiate an Observational Trial (the “Trial”) on patients treated with 3,4 Methylenedioxymethamphetamine (“MDMA”) through Health Canada’s Special Access Program (SAP). The Parties will each play an important role in the execution of this trial:
The announcement of the Trial comes following the release yesterday of the Senate of Canada’s Subcommittee on Veterans report, The Time is Now: Granting equitable access to psychedelic-assisted therapies, which urged Veterans Affairs Canada to increase research into the treatment of veterans’ “moral injuries” such as Post-Traumatic Stress Disorder with psychedelic molecules, including MDMA. This trial will generate Real World Evidence (“RWE”) on the efficacy of MDMA in the treatment of Post-Traumatic Stress Disorder which may be submitted to Health regulators, including Health Canada and Veterans Affairs Canada. The Parties hope that data collected in the Trial will add to the knowledge base of both regulators and the scientific community on the real-world evidence of efficacy and safety of these treatments.
The Parties’ initial submission to the Review Ethics Board has been approved, and the parties intend to proceed to data gathering immediately. Subsequent Ethics Review Board submissions are contemplated in the LOI. As the trial is Observational in nature, no patients will be dosed as part of the trial’s protocol. The goal of the trial is to gather data on the efficacy of treatment for patients who are already qualified for treatment under the Special Access Program.
“Our ability to treat patients through SAP, while imperfect, remains a credit to Canadian regulators and an incredibly valuable tool for the collection of evidence of MDMA’s efficacy in real-world clinical outcomes. We’re incredibly pleased to work with Dr. Mayo and Heroic Hearts to bring together patients, clinicians, and scientists,” said Nick Kadysh, CEO, PharmAla Biotech. “We are already seeing amazing results in patients, and we believe we are currently the only company in the world that can generate evidence from SAP which can be shared directly with regulators, as well as the scientific community.”
“While clinical evidence in the form of trial data on the efficacy of MDMA as a treatment for PTSD has been published – and is encouraging – this is a global first: an assessment of the efficacy of MDMA in treating PTSD outside the bounds of a clinical trial,” said Dr. Leah Mayo, Parker Psychedelics Research Chair, University of Calgary. “This observational trial is only possible due to the unique partnership of the 3 groups represented here, and the data gathered should significantly add to the body of knowledge around MDMA-assisted therapies.”
“Heroic Hearts Canada is committed to making MDMA-assisted therapy and other innovative psychedelic-assisted therapies accessible to veterans, who experience disproportionately high rates of trauma and mental illness after service,” said David Fascinato, Executive Director, of Heroic Hearts Canada. “This partnership is an important opportunity to add to the body of knowledge and support Health Canada and stakeholders such as Veterans Affairs Canada, in understanding the potential of MDMA-assisted therapy, with the goal of eventual approval so that it is accessible to all in need through approved healthcare channels.”
PharmAla Biotech Holdings Inc. (CSE: MDMA) is a biotechnology company focused on the research, development, and manufacturing of MDXX class molecules, including MDMA. PharmAla was founded with a dual focus: alleviating the global backlog of generic, clinical-grade MDMA to enable clinical trials, and to develop novel drugs in the same class. PharmAla is a “regulatory first” organization, formed under the principle that true success in the psychedelics industry will only be achieved through excellent relationships with regulators. Our team of dedicated professionals includes regulatory experts, scientists, and biomanufacturing professionals. PharmAla has built what it believes to be North America’s first cGMP MDMA value chain, encompassing GMP manufacturing of Active Pharmaceutical Ingredient (API), and drug product formulation. PharmAla’s research and development unit has also begun preclinical research into two patented Novel Chemical Entities (NCEs) based on MDXX class molecules, with proof-of-concept research currently ongoing at the University of Arkansas Medical School.
Nicholas Kadysh, CEO