| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 0.00 | 0.00 | 0.00 | 316.95K | 2.08M | 2.31M |
| Gross Profit | -352.65K | 0.00 | 0.00 | 158.83K | 926.89K | 1.03M |
| EBITDA | -62.81M | -63.69M | -58.06M | -51.47M | -33.73M | -17.00M |
| Net Income | -62.50M | -61.04M | -53.47M | -50.51M | -33.54M | -17.04M |
Balance Sheet | ||||||
| Total Assets | 241.06M | 52.71M | 102.58M | 122.37M | 166.70M | 38.42M |
| Cash, Cash Equivalents and Short-Term Investments | 227.56M | 36.14M | 85.67M | 105.52M | 149.20M | 37.09M |
| Total Debt | 3.92M | 4.16M | 4.46M | 4.84M | 5.36M | 621.09K |
| Total Liabilities | 13.08M | 11.33M | 12.01M | 12.52M | 10.72M | 60.90M |
| Stockholders Equity | 227.98M | 41.39M | 90.58M | 109.85M | 155.98M | -22.48M |
Cash Flow | ||||||
| Free Cash Flow | -50.04M | -55.08M | -49.31M | -44.84M | -30.91M | -14.67M |
| Operating Cash Flow | -50.01M | -55.00M | -48.97M | -44.10M | -30.85M | -14.62M |
| Investing Cash Flow | 5.47M | 26.43M | 7.30M | 41.83M | -75.62M | -53.41K |
| Financing Cash Flow | 226.90M | 5.30M | 28.44M | 19.00K | 144.26M | 37.98M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
56 Neutral | $720.52M | -5.15 | -67.94% | ― | 332.71% | 75.73% | |
52 Neutral | $286.04M | -2.60 | -43.75% | ― | ― | 9.32% | |
52 Neutral | $428.56M | -1.65 | -74.88% | ― | ― | 18.39% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
45 Neutral | $291.86M | -1.69 | -78.24% | ― | ― | -67.41% | |
42 Neutral | $334.03M | -2.65 | -64.26% | ― | ― | -11.41% |
On January 7, 2026, Immuneering announced updated interim results from its ongoing Phase 2a trial of atebimetinib, a once-daily oral MEK inhibitor, combined with modified Gemcitabine/nab-Paclitaxel in first-line pancreatic cancer patients, showing a 64% overall survival rate at 12 months as of the December 15, 2025 cutoff in a 34-patient intent-to-treat cohort at the 320 mg dose, compared with a reported 35% 12‑month overall survival for standard of care, with median overall survival not yet reached and median progression-free survival of 8.5 months. The regimen was generally well tolerated, with no Grade 5 treatment-emergent adverse events and no new safety signals, and Immuneering signaled a rapid development path by planning additional survival and circulating tumor DNA data readouts in 2026, as well as initiating a pivotal Phase 3 trial in first-line pancreatic cancer and a combination trial with Libtayo in non-small cell lung cancer, underscoring its bid to strengthen its position in oncology and potentially enhance treatment options for patients and clinicians.
The most recent analyst rating on (IMRX) stock is a Buy with a $12.00 price target. To see the full list of analyst forecasts on Immuneering stock, see the IMRX Stock Forecast page.