| Breakdown | Nov 2025 | Nov 2024 | Nov 2023 | Nov 2022 | Aug 2021 |
|---|---|---|---|---|---|
Income Statement | |||||
| Total Revenue | 605.50K | 1.04M | 532.00K | 78.07K | 0.00 |
| Gross Profit | -845.17K | 887.44K | 454.10K | 75.78K | -303.00 |
| EBITDA | -2.07M | -573.36K | -710.18K | -973.45K | -2.51M |
| Net Income | -2.18M | -823.60K | -779.81K | -985.58K | -2.51M |
Balance Sheet | |||||
| Total Assets | 3.42M | 2.90M | 2.41M | 2.33M | 2.79M |
| Cash, Cash Equivalents and Short-Term Investments | 960.66K | 419.38K | 195.04K | 852.14K | 2.47M |
| Total Debt | 0.00 | 0.00 | 253.54K | 0.00 | 0.00 |
| Total Liabilities | 961.73K | 916.88K | 1.03M | 423.78K | 138.48K |
| Stockholders Equity | 2.46M | 1.98M | 1.38M | 1.91M | 2.66M |
Cash Flow | |||||
| Free Cash Flow | -1.05M | -547.78K | -846.39K | -1.62M | -435.76K |
| Operating Cash Flow | -1.04M | -321.36K | -339.66K | -625.37K | -173.57K |
| Investing Cash Flow | -935.27K | -226.42K | -506.74K | -994.87K | 629.22K |
| Financing Cash Flow | 1.60M | 772.12K | 189.29K | 0.00 | 2.02M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
51 Neutral | C$5.59M | -0.19 | ― | ― | ― | 90.81% | |
49 Neutral | C$10.89M | -4.98 | -85.96% | ― | -72.51% | -170.13% | |
42 Neutral | C$11.74M | -3.64 | 21.59% | ― | ― | -120.00% | |
40 Underperform | C$8.65M | -5.79 | -112.32% | ― | ― | 27.35% |
PharmAla Biotech has signed a Supply & Data Agreement with Nautilus Sanctuary in New York to provide its LaNeo MDMA for a Phase 2 open-label clinical trial using MDMA-assisted therapy to treat post-traumatic stress and adjustment disorders in frontline healthcare workers and first responders. In exchange for donating the drug, PharmAla receives a perpetual, non-exclusive license to de-identified trial data for global regulatory and commercial use, reinforcing its supply-for-data model and expanding its evidence base for LaNeo MDMA, while also completing a separate LaNeo MDMA shipment to University College London for another clinical study.
The Nautilus trial underscores PharmAla’s strategy of supporting high-need mental health populations while building a robust portfolio of clinical data to cement its position as a key supplier of clinical-grade MDMA. By deepening its involvement in U.S. and U.K. research, the company strengthens its industry positioning in psychedelic-assisted therapies, potentially benefiting regulators, clinicians, and patients through accelerated evidence generation on MDMA’s safety and efficacy.
The most recent analyst rating on (TSE:MDMA) stock is a Hold with a C$0.09 price target. To see the full list of analyst forecasts on PharmAla Biotech Holdings, Inc. stock, see the TSE:MDMA Stock Forecast page.
PharmAla Biotech has signed a drug donation agreement with Spaulding Rehabilitation, part of the Mass General Brigham system, to supply its LaNeo MDMA at no cost for a clinical trial investigating MDMA-assisted therapy in fibromyalgia patients. In return, PharmAla will receive a license to the study results, which it can use for public applications such as potential regulatory submissions, while Spaulding retains first publication rights and control over independent intellectual property.
The study, led by Principal Investigator Vitaly Napadow in Boston, will use hyperscan neuroimaging to explore how MDMA-assisted therapy affects brain mechanisms related to pain relief and interpersonal dynamics in fibromyalgia, a chronic condition affecting about 4 million U.S. adults. The collaboration extends PharmAla’s clinical research footprint beyond PTSD into pain and complex, treatment-resistant conditions, potentially strengthening its position in psychedelic-derived therapeutics and expanding the evidence base for MDMA’s analgesic and neuromodulatory effects.
The most recent analyst rating on (TSE:MDMA) stock is a Hold with a C$0.10 price target. To see the full list of analyst forecasts on PharmAla Biotech Holdings, Inc. stock, see the TSE:MDMA Stock Forecast page.
PharmAla Biotech Holdings has signed a binding supply agreement with Amsterdam University Medical Center in the Netherlands to provide LaNeo 40 mg MDMA capsules for a proposed clinical trial. The product will be repackaged into a new single-capsule format as part of the collaboration.
The agreement includes a three-year stability testing program for the single-capsule dosage, designed to generate data needed to develop commercial-grade blister packaging for LaNeo MDMA. This initiative strengthens PharmAla’s European clinical presence and supports its broader commercial strategy by paving the way for more standardized, efficient distribution to research and treatment sites worldwide.
PharmAla already maintains a European value chain to supply LaNeo MDMA for clinical research, and the Amsterdam UMC deal is subject to a separate quality agreement and regulatory approvals. The company continues to position itself as a key provider of clinical-grade MDMA and related molecules to researchers and commercial partners across multiple jurisdictions.
The most recent analyst rating on (TSE:MDMA) stock is a Hold with a C$0.10 price target. To see the full list of analyst forecasts on PharmAla Biotech Holdings, Inc. stock, see the TSE:MDMA Stock Forecast page.
PharmAla Biotech Holdings Inc., a specialist in MDMA and MDXX-class psychedelic molecules, develops and manufactures clinical-grade compounds for research and patient treatments while advancing proprietary candidates such as its lead asset ALA-002. The company positions itself as a key supplier to clinical trials and regulated markets, emphasizing close collaboration with regulators as a competitive advantage.
PharmAla has reshaped its board of directors, accepting the resignation of long-time director Dr. Malik Slassi and appointing Montreal-based financial executive Lennie Ryer. Management highlighted Ryer’s deep experience in corporate finance, public-market transitions, and capital raising in life sciences and technology, signaling a push to strengthen governance and financial strategy as PharmAla moves into its next phase of growth.
The most recent analyst rating on (TSE:MDMA) stock is a Hold with a C$0.10 price target. To see the full list of analyst forecasts on PharmAla Biotech Holdings, Inc. stock, see the TSE:MDMA Stock Forecast page.
PharmAla Biotech has signed a supply agreement with Norway’s Østfold Hospital Trust to provide its LaNeo-branded MDMA for clinical research into MDMA as a potential treatment for major depressive disorder, following a competitive vendor review and extensive due diligence. The deal, which includes both financial and data-sharing components, underscores PharmAla’s strengthening role in Europe’s psychedelic medicine research ecosystem and leverages its established regional value chain, while also enhancing its clinical footprint by encouraging researchers to transition existing trial protocols to its LaNeo MDMA platform through dedicated support tools and potential data-sharing discounts.
The most recent analyst rating on (TSE:MDMA) stock is a Hold with a C$0.11 price target. To see the full list of analyst forecasts on PharmAla Biotech Holdings, Inc. stock, see the TSE:MDMA Stock Forecast page.
PharmAla Biotech Holdings has released its audited financial statements for the fiscal year ended August 31, 2025, along with unaudited results for the first quarter of fiscal 2026, highlighting steady growth in customer deposits tied to its LaNeo MDMA clinical trial supply business. Customer deposits rose to $276,000 at year-end 2025 and further to $433,000 in Q1 2026, reflecting expanding demand for LaNeo MDMA, particularly in Australia where medical treatments using the product are now reimbursed by private insurers and the Department of Veterans Affairs. Management emphasized that the growing pipeline of clinical trial sales, combined with a recently filed short-form prospectus and an Australian lending partner, will help fund the company’s development efforts and its planned Phase 2a/b clinical trial in Australia, underscoring PharmAla’s strategy to translate its regulatory-first posture and unique supply position into accelerated growth in the psychedelics therapeutics market.
PharmAla Biotech Holdings Inc. has announced that its subsidiary, PharmAla Biotech Australia, has contracted with a UK-based CDMO for the manufacturing of its ALA-002 drug substance. This strategic move is crucial for the company’s upcoming Phase 2 clinical trial in 2026, marking the development of a new Active Pharmaceutical Ingredient for human use since 2022. Additionally, PharmAla has completed a significant shipment of its LaNeo MDMA to Mount Sinai’s Parsons Research Center for clinical research, reinforcing its commitment to advancing psychedelic healing.
PharmAla Biotech Holdings Inc. has completed release testing of its first Australian-made batch of LaNeo™ MDMA 40mg capsules, marking a significant step in their production capabilities and market expansion. The company also finalized its contract with the Orygen Institute by delivering the last shipment of its Australian-made product to support a Phase 3 Trial on social anxiety in autistic youth, highlighting its commitment to advancing clinical research and its strategic positioning in the global psychedelics market.