Health Care
Emyria Limited (EMD)
Emyria Limited is a data-backed clinical drug development company operating in Australia. It runs a network of specialist medical clinics (Emerald Clinics) that gather proprietary Real-World Evidence from patients using unregistered medicines like cannabinoids. This data is then used to develop its own drug candidates and advance its programs in psychedelic-assisted therapies, most notably an MDMA-assisted therapy program for Post-Traumatic Stress Disorder (PTSD).
Market Cap
A$47M
Shares on Issue
N/A
Price Chart
AI Analysis
With a market capitalisation of approximately A$47M, Emyria is a speculative, clinical-stage biotechnology company. Its current business is twofold: generating initial revenue and valuable data from its clinical services, while investing heavily in its drug development pipeline. The company is currently loss-making, as is typical for the sector, and its financial performance is dictated by its cash burn rate relative to the progress of its expensive clinical trials. Recent share price performance is highly sensitive to news flow regarding its clinical programs, particularly its high-profile MDMA therapy trial.
Emyria's growth outlook is directly tied to achieving key clinical and regulatory milestones. The most significant near-term catalyst is the outcome of its Phase 2b clinical trial of MDMA-assisted therapy for PTSD. Positive results could serve as a major value inflection point and attract significant investor and partner interest. Longer-term growth depends on successfully navigating the regulatory pathway for its cannabinoid drug candidates (EMD-003 and EMD-004) and securing partnerships or licensing deals to commercialise its assets, while managing the ongoing need for capital to fund its research and development.
The strategic direction is to leverage its unique Real-World Evidence platform to de-risk and accelerate drug development, creating a competitive advantage over traditional biotech firms.
Bull Case
- • First-mover advantage in Australian psychedelic-assisted therapy with an active MDMA trial for PTSD, targeting a large and underserved market.
- • Unique data-driven drug development model using Real-World Evidence from its clinics, which can de-risk clinical trials and accelerate registration pathways.
- • A diversified pipeline with multiple potential catalysts across both psychedelic and cannabinoid-based treatments for different indications.
Bear Case
- • High clinical trial failure risk, where negative results from its key MDMA or cannabinoid programs would severely impact the company's valuation.
- • Significant cash burn and reliance on future capital raisings to fund operations, which can lead to shareholder dilution.
- • Uncertain and evolving regulatory landscape for both psychedelic and cannabinoid-based medicines, creating potential delays and commercialisation hurdles.
Recent Announcements
Euroz Hartleys 2026 Healthcare Forum
Application for quotation of securities - EMD
Emyria's PTSD Program Delivers Lasting Recovery
🚨 Price SensitiveEmyria Pharmaceuticals (ASX: EMD) reports a successful clinical trial for its innovative PTSD treatment, showing lasting recovery in patients. Investors are advised to monitor the company' extraditional developments closely as this could significantly impact
Emyria's Quarterly Investor Webinar
December 2025 Quarterly Activities Report and Appendix 4C
🚨 Price SensitiveEMD, a commitments test entity on ASX, has released its quarterly report for December 2025 detailing financial activities and is required to submit an appendix as per regulatory guidelines. Investors are advised to review the document' end-of-
FAQs
What does EMD do?
Emyria is a clinical-stage biotechnology company that uses data from its network of medical clinics to develop new drugs. It focuses on two main areas: developing cannabinoid-based medicines for conditions like anxiety and IBS, and pioneering psychedelic-assisted therapies, with a leading program using MDMA to treat PTSD.
Is EMD a good investment?
EMD is a high-risk, high-reward speculative investment. The potential upside is substantial if its drug development programs, particularly the MDMA therapy trial, succeed and gain regulatory approval. However, the risks are equally high, including the possibility of clinical trial failure, regulatory roadblocks, and the need for future dilutive funding.
What drives EMD's share price?
The share price is primarily driven by news and catalysts from its clinical pipeline. Key drivers include clinical trial results, ethics and regulatory approvals (like from the TGA), patent grants, research publications, and announcements regarding funding or strategic partnerships.
Key Metrics
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