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Psyence Biomedical Ltd. SEC Filings

PBM NASDAQ

Welcome to our dedicated page for Psyence Biomedical Ltd. SEC filings (Ticker: PBM), a comprehensive resource for investors and traders seeking official regulatory documents including 10-K annual reports, 10-Q quarterly earnings, 8-K material events, and insider trading forms.

Parsing Psyence Biomedical’s SEC disclosures isn’t easy—clinical-trial protocols, Schedule I psilocybin controls, and detailed R&D burn tables fill hundreds of pages. If you need a clear view of how much runway remains before Phase 2 data or want to monitor directors’ stock sales, navigating the raw documents can feel overwhelming.

Stock Titan turns that tangle into insight. Our AI-powered summaries translate each Psyence Biomedical annual report 10-K into plain English, flagging key risk factors and psilocybin manufacturing milestones. Get real-time alerts the moment a Psyence Biomedical 8-K material events filing drops, or track Psyence Biomedical insider trading Form 4 transactions without refreshing EDGAR. Looking for quarter-over-quarter cash flow? The Psyence Biomedical quarterly earnings report 10-Q filing is paired with concise revenue, R&D expense, and clinical-trial pipeline tables—ideal for comparing progress across periods.

Whether you’re checking Psyence Biomedical executive stock transactions Form 4, studying the proxy statement executive compensation details, or simply understanding Psyence Biomedical SEC documents with AI, every filing type is covered and cross-linked. Investors use these insights to spot insider sentiment before pivotal readouts, gauge dilution risk from shelf registrations, and follow licensing revenue reported in 8-Ks. Stop wading through PDFs—our AI explains Psyence Biomedical SEC filings simply while preserving every number you need.

Rhea-AI Summary

Psyence Biomedical (Nasdaq: PBM) filed its FY-2025 Form 20-F covering the year ended March 31 2025.

Key disclosures include:

  • 568,021 common shares outstanding at year-end
  • Securities trade as PBM (shares) and PBMWW (warrants) on Nasdaq
  • Reports under IFRS; classified as a non-accelerated filer and emerging growth company
  • Not a well-known seasoned issuer; no SOX 404(b) auditor attestation
  • Company has no products yet approved for commercial sale and depends on successful clinical trials and regulatory clearance
  • Forward-looking statements flag risks around Nasdaq listing stability, share price volatility, talent retention, supply chain, IP licensing and macro conditions

The filing provides full audited financials, risk factors and corporate-governance disclosures but does not announce new financings, M&A or product approvals.

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FAQ

What is the current stock price of Psyence Biomedical Ltd. (PBM)?

The current stock price of Psyence Biomedical Ltd. (PBM) is $4.91 as of June 28, 2025.

What is the market cap of Psyence Biomedical Ltd. (PBM)?

The market cap of Psyence Biomedical Ltd. (PBM) is approximately 2.8M.

What is the core business of Psyence Biomedical Ltd.?

Psyence Biomedical focuses on developing nature-derived psilocybin products for mental health treatments. The company specializes in integrating clinical trials with advanced biopharmaceutical manufacturing.

How does Psyence Biomedical produce its psilocybin-based products?

The company cultivates natural psilocybin mushrooms at a federally licensed facility in Southern Africa. These raw materials are processed into high-purity, pharmaceutical-grade products for clinical evaluation.

What clinical trials is the company currently conducting?

Psyence Biomedical is conducting randomized, double-blind, placebo-controlled trials to assess the efficacy of psilocybin therapies. These trials target conditions such as Adjustment Disorder in palliative care and Alcohol Use Disorder.

What role do partnerships play in the company’s strategy?

Strategic partnerships with organizations like Fluence, iNGENū CRO, and PsyLabs are integral to Psyence Biomedical’s approach. These collaborations provide essential expertise in clinical trial management, regulatory compliance, and high-purity compound production.

How does the company ensure safety and efficacy in its products?

Psyence Biomedical adheres to rigorous clinical trial protocols and quality control measures. Its vertically integrated model ensures that every stage of product development meets strict regulatory standards and scientific benchmarks.

How does Psyence Biomedical differentiate itself within the biotech sector?

The company differentiates itself through its emphasis on natural, high-purity psilocybin and its comprehensive integration of research, manufacturing, and clinical execution. This approach allows for more controlled processes and high standards in therapeutic development.

What market segments does the company target?

Psyence Biomedical primarily targets patients in palliative care and individuals suffering from mental health and substance use disorders. Its therapeutic focus extends to addressing unmet clinical needs in mental health through innovative psychedelic treatments.

How does the company’s vertical integration benefit its operations?

Vertical integration allows Psyence Biomedical to maintain control over every aspect of the therapeutic development process, from cultivation to clinical trials. This integration supports operational efficiency and reinforces the company’s commitment to quality and regulatory compliance.
Psyence Biomedical Ltd.

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