Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|---|
Income Statement | ||||||
Total Revenue | 2.53M | 2.29M | 1.60M | 1.67M | 2.00M | 2.10M |
Gross Profit | 1.51M | 1.02M | 662.00K | 983.00K | 1.16M | 1.47M |
EBITDA | -16.90M | -11.97M | -13.96M | -7.18M | -6.38M | -8.76M |
Net Income | -21.38M | -15.40M | -15.66M | -11.28M | -8.79M | -9.10M |
Balance Sheet | ||||||
Total Assets | 5.50M | 5.32M | 5.21M | 12.00M | 11.55M | 8.16M |
Cash, Cash Equivalents and Short-Term Investments | 3.10M | 2.99M | 2.95M | 8.41M | 8.89M | 5.81M |
Total Debt | 17.60M | 14.93M | 8.56M | 7.57M | 582.00K | 667.00K |
Total Liabilities | 45.67M | 32.87M | 21.76M | 14.55M | 7.47M | 8.83M |
Stockholders Equity | -40.18M | -27.55M | -16.55M | -2.55M | 4.08M | -669.00K |
Cash Flow | ||||||
Free Cash Flow | -10.72M | -8.85M | -10.91M | -9.93M | -9.18M | -639.00K |
Operating Cash Flow | -9.35M | -8.82M | -10.72M | -9.90M | -8.70M | -324.00K |
Investing Cash Flow | -170.00K | -27.00K | -185.00K | -33.00K | -325.00K | -297.00K |
Financing Cash Flow | 5.08M | 8.88M | 5.44M | 9.46M | 12.16M | 5.18M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
60 Neutral | C$91.94M | 69.34 | 1.88% | ― | 0.03% | -17.30% | |
54 Neutral | C$186.93M | ― | -106.37% | ― | 64.42% | -21.09% | |
53 Neutral | C$76.97M | ― | -69.80% | ― | ― | 55.80% | |
51 Neutral | $7.83B | -0.18 | -40.10% | 2.29% | 21.46% | -2.03% | |
51 Neutral | C$388.71M | ― | 80.28% | ― | 33.19% | -13.73% | |
44 Neutral | C$21.01M | ― | ― | 0.78% | 2.86% | ||
26 Underperform | C$109.74M | ― | 90.17% | ― | ― | -37.72% |
Spectral Medical and Vantive announced positive topline results from the Tigris trial, a Phase 3 study evaluating PMX Hemoadsorption Therapy for endotoxic septic shock. The trial demonstrated a significant reduction in 28-day and 90-day mortality rates, exceeding the prespecified primary endpoint with a high probability of benefit, which could enhance Spectral’s positioning in the sepsis treatment market.
Spectral Medical announced significant progress in its clinical and operational efforts during the second quarter of 2025, particularly with the completion of patient enrollment in the Tigris trial. The company is on track to release topline results for this Phase III trial, which evaluates PMX for endotoxic septic shock, by mid-August 2025. These results are crucial for the company’s Premarket Approval submission to the FDA. Spectral has also secured non-dilutive funding from its partner Vantive, aiding its financial stability and readiness for potential FDA approval and commercialization. The company’s efforts are aligned with market readiness and regulatory timelines, indicating a strategic focus on execution across regulatory, clinical, and commercial fronts.
Spectral Medical Inc. has filed a preliminary short form base shelf prospectus with Canadian securities regulators, excluding Québec, to qualify the distribution of up to $100 million in various securities over a 25-month period. This move is intended to provide the company with financial flexibility as it approaches significant milestones, though it is not an immediate indication of capital raising. The filing underscores Spectral’s strategy to optimize its balance sheet and maintain operational agility amid its ongoing efforts to secure FDA approval for its septic shock treatment.
Spectral Medical Inc. announced the successful results of its Annual Meeting of Shareholders, where all proposed resolutions were approved, including the election of seven directors and the re-appointment of MNP LLP as auditors. This outcome reinforces the company’s governance structure and supports its ongoing efforts to advance its flagship product, Toraymyxin™ (PMX), towards FDA approval. The confirmation of these resolutions and the continued support from shareholders are crucial as Spectral progresses with its Tigris Trial, a pivotal study for PMX, potentially strengthening its position in the biomedical industry.
Spectral Medical Inc. announced its participation in the 3rd Annual H.C. Wainwright BioConnect Investor Conference, highlighting its ongoing efforts to secure U.S. FDA approval for its septic shock treatment, Toraymyxin™. The company’s involvement in the conference underscores its strategic initiatives to engage with investors and stakeholders, potentially impacting its market positioning and future growth in the biomedical industry.