| Breakdown | TTM | Dec 2025 | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 |
| Gross Profit | 0.00 | 0.00 | -711.00 | -1.42K | -1.78K | -355.00 |
| EBITDA | -1.65M | -1.52M | -3.04M | -3.96M | -3.96M | -2.43M |
| Net Income | -1.59M | -1.53M | -3.12M | -6.42M | -4.01M | 2.66M |
Balance Sheet | ||||||
| Total Assets | 1.26M | 1.34M | 2.59M | 6.31M | 12.16M | 5.94M |
| Cash, Cash Equivalents and Short-Term Investments | 1.04M | 1.12M | 2.30M | 6.25M | 12.12M | 5.88M |
| Total Debt | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 |
| Total Liabilities | 472.86K | 366.33K | 252.90K | 892.48K | 330.32K | 361.06K |
| Stockholders Equity | 784.35K | 973.54K | 2.34M | 5.42M | 11.83M | 5.58M |
Cash Flow | ||||||
| Free Cash Flow | -1.11M | -1.21M | -3.52M | -3.24M | -3.51M | 917.92K |
| Operating Cash Flow | -1.11M | -1.21M | -3.52M | -3.24M | -3.51M | 922.19K |
| Investing Cash Flow | 0.00 | 0.00 | -300.00K | 0.00 | 0.00 | 214.77K |
| Financing Cash Flow | 250.00K | 0.00 | 35.00K | 0.00 | 9.89M | 1.25M |
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% | |
45 Neutral | C$9.10M | -5.62 | -112.32% | ― | ― | 27.35% | |
43 Neutral | C$17.80M | -3.78 | ― | ― | 95.76% | 22.56% | |
43 Neutral | C$18.90M | -0.15 | -409.25% | ― | ― | 62.01% | |
41 Neutral | C$16.96M | -3.09 | ― | ― | ― | -24.89% |
PharmaTher CEO Fabio Chianelli outlined how 2025 marked a transition from development to validation, highlighted by U.S. FDA approval of the company’s ketamine ANDA and its subsequent sale in a deal structured with upfront payments, milestones and profit-sharing that could exceed US$25 million. With reduced cash burn, a lean operating structure and expected receipts from the ketamine ANDA sale, PharmaTher says it is positioned to pursue 2026 goals without raising additional operating funds, focusing on international ketamine commercialization, strategic partnerships in Parkinson’s disease and drug delivery, monetization of its stake in Sairiyo Therapeutics, and development of next-generation and long-acting ketamine programs and platform tools such as KetaVault and KetAImine to accelerate asset monetization and strengthen its position as an asset-focused value creation company.
The most recent analyst rating on (TSE:PHRM) stock is a Hold with a C$0.10 price target. To see the full list of analyst forecasts on PharmaTher Holdings Ltd stock, see the TSE:PHRM Stock Forecast page.
PharmaTher Holdings Ltd. has completed the sale of its Abbreviated New Drug Application for Ketamine Hydrochloride Injection USP, receiving an upfront cash payment and potential future milestone and profit-sharing payments. This move allows PharmaTher to concentrate on its long-acting injectable ketamine program, which aims to provide a more convenient and effective treatment option for neuropsychiatric disorders, potentially improving patient adherence and expanding market access.
PharmaTher Holdings Ltd. has entered into an exclusive agreement with Oakwood Laboratories to evaluate and potentially license a patented long-acting injectable ketamine program. This initiative is part of PharmaTher’s strategy to enhance its ketamine franchise by offering a differentiated product that could redefine treatment standards for neuropsychiatric disorders. The program aims to provide more convenient dosing, improve patient adherence, and expand access to ketamine-based therapies, potentially offering significant commercial and strategic advantages.
PharmaTher Holdings Ltd. applauds the FDA’s selection of ketamine as a national priority under the Commissioner’s National Priority Voucher (CNPV) pilot program, which is expected to boost demand for ketamine in the U.S. The company is strategically positioned to benefit from this development through its previous ANDA sale, which allows for economic participation without significant capital investment. This move aligns with PharmaTher’s capital-light strategy, potentially accelerating its 505(b)(2) ketamine-based programs and enhancing its market positioning.
PharmaTher Holdings Ltd. is advancing its Phase 3 FDA package for the use of ketamine in treating levodopa-induced dyskinesia in Parkinson’s disease. The company is preparing for a meeting with the FDA to align on a single, well-controlled Phase 3 study under the 505(b)(2) pathway. This strategic move aims to leverage existing clinical evidence and intellectual property, with the potential to tap into a significant market opportunity estimated at US$0.75-$2.2 billion. The company is also in discussions with potential partners for co-development and licensing, which could accelerate timelines and optimize commercial reach.
PharmaTher Holdings Ltd. has announced the launch of KetAImine™, an AI-driven platform designed to expand its ketamine portfolio and accelerate FDA approval processes. This initiative aims to unlock new medical indications and create partnering opportunities by discovering novel uses and drug combinations with ketamine. The platform, part of PharmaTher’s Digital Health AI division, will enhance the company’s market positioning by enabling earlier partnerships and fast-tracking regulatory pathways, potentially benefiting stakeholders through quicker access to innovative therapies.