Psyence Biomedical Ltd. has received formal approval from the Bellberry Human Research Ethics Committee (HREC) for the use of PsyLabs' psilocybin product (NPX5) in its ongoing Phase IIb clinical trial. This approval allows Psyence BioMed to utilize PsyLabs' nature-derived, GMP-compliant psilocybin as the investigational product in a double-blind, randomized, low-dose comparator-controlled study evaluating psilocybin-assisted psychotherapy for Adjustment Disorder in cancer patients. The authorization applies to all participating study sites, with additional sites planned to accelerate patient recruitment and advance the trial. No other organizations are mentioned as recipients of this approval.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Psyence Biomedical Ltd. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9605101-en) on December 19, 2025, and is solely responsible for the information contained therein.
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