| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 |
| Gross Profit | 0.00 | 0.00 | -298.59K | -301.11K | -360.57K | -332.65K |
| EBITDA | -35.41M | -34.88M | -20.19M | -18.71M | -20.58M | -16.45M |
| Net Income | -35.27M | -31.71M | -20.56M | -19.08M | -20.98M | -16.78M |
Balance Sheet | ||||||
| Total Assets | 15.06M | 20.19M | 38.82M | 37.33M | 45.88M | 34.35M |
| Cash, Cash Equivalents and Short-Term Investments | 12.35M | 15.94M | 34.91M | 32.14M | 41.26M | 31.22M |
| Total Debt | 835.00K | 1.06M | 423.00K | 373.00K | 655.00K | 402.06K |
| Total Liabilities | 14.94M | 14.20M | 11.26M | 10.83M | 9.78M | 9.59M |
| Stockholders Equity | 115.00K | 5.98M | 27.56M | 26.50M | 36.10M | 24.75M |
Cash Flow | ||||||
| Free Cash Flow | -26.48M | -27.20M | -28.46M | -23.41M | -22.72M | -22.10M |
| Operating Cash Flow | -26.47M | -26.97M | -28.45M | -23.36M | -22.43M | -22.07M |
| Investing Cash Flow | -13.00K | -239.00K | 20.22M | -20.40M | -285.95K | -29.30K |
| Financing Cash Flow | 18.74M | 6.64M | 31.99M | 12.21M | 33.02M | 39.77M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
62 Neutral | $138.91M | 0.57 | 27.20% | ― | ― | 814.20% | |
60 Neutral | $188.38M | -2.24 | -129.98% | ― | 250.00% | 15.15% | |
53 Neutral | $189.30M | -1.02 | -51.49% | ― | -33.76% | 17.54% | |
52 Neutral | $102.23M | -3.43 | -755.18% | ― | ― | ― | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
43 Neutral | $45.90M | -3.22 | -49.42% | ― | ― | -9.42% | |
42 Neutral | $40.15M | 6.94 | -79.12% | ― | 51.27% | ― |
On March 2, 2026, Oncolytics Biotech Inc. announced the launch of REO 033, a randomized Phase 2 study in second-line RAS-mutated, microsatellite-stable metastatic colorectal cancer, comparing standard bevacizumab plus FOLFIRI to an experimental arm adding pelareorep, with 30 patients per arm and objective response rate as the primary endpoint. The trial, led by Rutgers Cancer Institute’s Dr. Sanjay Goel and expected to open its first site later in March with preliminary data targeted by year-end, aims to confirm earlier REO 022 results in the same population, where pelareorep-based therapy showed substantially improved survival and response rates over standard of care, underscoring pelareorep’s emerging role in colorectal cancer and potentially strengthening Oncolytics’ position in gastrointestinal oncology.
The most recent analyst rating on (ONCY) stock is a Buy with a $7.00 price target. To see the full list of analyst forecasts on Oncolytics Biotech stock, see the ONCY Stock Forecast page.
On February 24, 2026, Oncolytics Biotech announced it had concluded enrollment in its GOBLET gastrointestinal cancer study and would wind down the trial after gathering sufficient clinical and translational data to guide next steps. With adequate cash to meet near-term milestones, the company said it will now concentrate resources on registrational and registration-enabling programs in squamous cell anal cancer and metastatic colorectal cancer in the U.S.
Management highlighted that efficacy seen in GOBLET’s anal cancer cohort has defined a regulatory path for pelareorep in second-line and later squamous cell anal cancer, and Oncolytics plans a U.S.-based, single-arm registrational study involving fewer than 100 patients. As part of this sharper focus, the company has halted further enrollment in the metastatic pancreatic ductal adenocarcinoma cohort at about 20 patients per arm, continuing only to follow existing participants so it can analyze survival and response outcomes while limiting additional spending on that indication.
Executives framed the move as a disciplined capital-allocation strategy intended to pursue approvals in high-need gastrointestinal cancers and enhance shareholder value without immediate material dilution. The GOBLET data set, generated at 17 centers in Germany, is described as having validated pelareorep’s platform potential in GI tumors and provided a clearer, more efficient roadmap for registration-focused development in colorectal, anal and potentially other gastrointestinal cancers, with implications for the company’s regulatory trajectory and competitive positioning in oncology.
The most recent analyst rating on (ONCY) stock is a Buy with a $7.00 price target. To see the full list of analyst forecasts on Oncolytics Biotech stock, see the ONCY Stock Forecast page.
On February 4, 2026, Oncolytics Biotech announced that the U.S. Food and Drug Administration granted Fast Track Designation for pelareorep in combination with bevacizumab and FOLFIRI as a second-line treatment for KRAS‑mutant, microsatellite-stable metastatic colorectal cancer, following an application submitted after a strategic shift toward gastrointestinal cancers. The designation is backed by clinical data showing a 33% objective response rate, median progression-free survival of 16.6 months, and median overall survival of 27 months for the pelareorep regimen, roughly double to triple standard-of-care outcomes in this difficult-to-treat patient group, which represents a global total addressable market estimated at $3‑5 billion annually. Oncolytics plans to initiate a controlled clinical study in this indication, with the first site expected to open in March and interim data targeted by year-end 2026, positioning pelareorep as a potentially important platform immunotherapy in gastrointestinal oncology and giving the company enhanced regulatory interaction that could expedite development timelines.
The most recent analyst rating on (ONCY) stock is a Hold with a $0.98 price target. To see the full list of analyst forecasts on Oncolytics Biotech stock, see the ONCY Stock Forecast page.
On January 7, 2026, Oncolytics Biotech expanded its Gastrointestinal Tumor Scientific Advisory Board by appointing three high-profile gastrointestinal oncology experts—Drs. Eileen O’Reilly and Neil Segal of Memorial Sloan Kettering Cancer Center and Dr. Van Morris of MD Anderson Cancer Center—to help guide the late-stage clinical and strategic development of pelareorep as a platform immunotherapy across pancreatic, colorectal, and anal cancers. With the GI advisory board now comprising six global leaders, the company is reinforcing its clinical and strategic infrastructure as it prepares registration-enabling trials in these high-value indications, underpinned by earlier clinical data suggesting improved survival and response rates versus historical benchmarks in first-line pancreatic cancer, squamous cell anal carcinoma, and KRAS-mutant metastatic colorectal cancer—positioning Oncolytics to potentially enhance its competitive standing in GI oncology and attract greater attention from larger pharmaceutical players.
The most recent analyst rating on (ONCY) stock is a Hold with a $0.87 price target. To see the full list of analyst forecasts on Oncolytics Biotech stock, see the ONCY Stock Forecast page.