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Psyence BioMed Announces Approval for Use of PsyLabs’ Psilocybin Product in Phase IIb Clinical Trial

With approximately $9.5 million in cash reserves and no debt, the Company is ready to leverage strengthened vertical integration as clinical-grade psilocybin moves into Phase IIb trialsNEW YORK, Dec. 19, 2025 (GLOBE NEWSWIRE) -- Psyence Biomedical Ltd. (Nasdaq: PBM) (“Psyence BioMed” or the “Company”), a biopharmaceutical company advancing nature-derived psilocybin and ibogaine therapies for unmet mental health needs, today announced that the Bellberry Human Research Ethics Committee (HREC) has

articlePsyence Biomedical Ltd.December 19, 20257/company/psyence-biomedical-ltd-common-shares/news/psyence-biomed-announces-approval-psylabs-120000015
Psyence BioMed Announces Approval for Use of PsyLabs’ Psilocybin Product in Phase IIb Clinical Trial

About this update from Psyence Biomedical Ltd.

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More updates from Psyence Biomedical Ltd.

The CompanyPsyence Biomedical Ltd.Phase IIbclinical developmentbiopharmaceutical companypsilocybin mushroomsvertically integratedinvestigational productBioMedCompany