This randomised, double-blind, placebo-controlled trial (n=32) will investigate the safety, tolerability, pharmacokinetics, and pharmacodynamics of single-ascending doses of EMP-01 (ar-MDMA) in healthy adult volunteers.
EMP-01 is being developed as a potential treatment for post-traumatic stress disorder (PTSD). The study will consist of 4 cohorts, each with 8 participants, who will receive different doses of EMP-01 or placebo. Safety and tolerability will be assessed through adverse events monitoring and safety laboratory tests. Pharmacokinetic parameters will be evaluated, including plasma concentration and urine analysis of EMP-01 and its major metabolite.
Participants must meet specific inclusion criteria, including being aged between 18 and 55, in good health, and willing to abstain from certain medications and substances during the study period.
The trial is conducted at New Zealand Clinical Research and is sponsored by EmpathBio Australia Pty. Ltd. The principal investigator is Dr Christian Schwabe. The study was registered on ANZCTR with the registration number ACTRN12622001335785 and has been approved by the Central Health and Disability Ethics Committees in New Zealand.
Recruitment for the trial was completed, with the first participant enrolled on May 16, 2023, and the last participant enrolled on July 27, 2023. The study’s primary purpose is treatment-focused, aiming to provide critical data for the ongoing development of EMP-01 in the treatment of PTSD.
Trial Details
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Sponsors & Collaborators
EmpathBioEmpathBio is looking to develop MDMA analogues that are both patent-able and should be easier to administer (e.g. shorter duration, with digital/virtual care). EmpathBio is a subsidiary of ATAI.
atai Life Sciences
atai Life Sciences is one of the biggest companies in the psychedelics field. The company aims to be a platform and has nine subsidiary companies working on everything from psilocybin for depression to DMT administration.