| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 1.00M | 1.03M | 1.07M | 1.14M | 780.64K | 929.12K |
| Gross Profit | 493.77K | 554.03K | 562.13K | 628.17K | 309.94K | 269.68K |
| EBITDA | -4.07M | -3.96M | -4.25M | -4.90M | -4.31M | -5.56M |
| Net Income | -4.35M | -4.26M | -4.57M | -5.25M | -4.42M | -5.61M |
Balance Sheet | ||||||
| Total Assets | 3.00M | 3.25M | 3.28M | 4.16M | 5.94M | 10.02M |
| Cash, Cash Equivalents and Short-Term Investments | 80.99K | 268.76K | 43.91K | 1.51M | 3.69M | 7.88M |
| Total Debt | 319.72K | 293.87K | 386.88K | 473.62K | 35.72K | 92.34K |
| Total Liabilities | 1.91M | 1.18M | 1.37M | 1.07M | 874.79K | 857.13K |
| Stockholders Equity | 1.09M | 2.07M | 1.91M | 3.09M | 5.07M | 9.16M |
Cash Flow | ||||||
| Free Cash Flow | -2.61M | -3.35M | -4.11M | -5.20M | -4.13M | -4.61M |
| Operating Cash Flow | -2.52M | -3.33M | -4.07M | -5.13M | -4.03M | -4.45M |
| Investing Cash Flow | -97.89K | -19.97K | -37.27K | -70.41K | -100.82K | -164.58K |
| Financing Cash Flow | 2.36M | 3.57M | 2.65M | 3.02M | -57.37K | -57.56K |
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% | |
47 Neutral | C$39.84M | -9.14 | -269.41% | ― | 1.46% | 6.91% | |
47 Neutral | C$21.86M | -11.36 | -31.12% | ― | 9.71% | -118.02% | |
46 Neutral | C$31.91M | -1.34 | -181.70% | ― | 209.29% | 35.38% | |
45 Neutral | C$2.61M | -0.59 | ― | ― | 207.90% | -23.09% | |
44 Neutral | C$19.29M | -4.64 | ― | ― | 28.59% | 23.46% | |
40 Underperform | C$62.96M | -10.28 | -188.03% | ― | ― | -52.41% |
Theralase Technologies Inc. has announced a brokered private placement offering to raise between C$4.5 million and C$5.5 million, with Research Capital Corporation as the sole agent. The funds will primarily support a Phase II clinical study for non-muscle invasive bladder cancer and other strategic initiatives, potentially enhancing Theralase’s market position in cancer treatment.
Theralase Technologies Inc. has announced an investor conference call to update on its Phase II clinical study for BCG-Unresponsive Non-Muscle Invasive Bladder Cancer. The study shows promising interim results, with a 64.3% complete response rate among patients. Financially, the company reported a slight decrease in revenue and an increase in net loss for the nine months ended September 30, 2025. Despite these financial challenges, Theralase continues to pursue funding opportunities to support its clinical and commercial objectives.
Theralase Technologies Inc. has released its unaudited financial statements for the third quarter of 2025, reporting a 5% decrease in total revenue compared to the previous year. Despite a slight decrease in gross margin and an increase in net loss, the company continues to make progress in its clinical trials, with significant advancements in Study II. The company completed a private placement and extended warrant expiry dates to support its financial position, while also exploring additional funding opportunities. The ongoing clinical study has shown promising interim results, with a high percentage of patients achieving a complete or total response, indicating strong treatment durability.
Theralase Technologies announced promising preclinical results for their X-Ray-activated drug, Rutherrin®, which has shown significant effectiveness in treating various cancers. The drug, when activated by radiation therapy, demonstrated enhanced tumor destruction, overcoming treatment resistance, and stimulating systemic immunity. These findings position Rutherrin® as a potential breakthrough in cancer treatment, with plans for further toxicology studies and clinical development targeting several aggressive cancers.
Theralase Technologies announced the publication of independent preclinical data showcasing the effectiveness of its antiviral candidate, Ruvidar®, in combating Herpes Simplex Virus Type 1 (HSV-1). The study highlights Ruvidar®’s superior performance compared to Acyclovir® and Metformin®, offering significant inhibitory effects on the virus without the need for light activation. This positions Ruvidar® as a promising next-generation antiviral therapy, particularly for drug-resistant HSV-1 infections, and supports its advancement into clinical development.