Breakdown | |||||
TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|
Income Statement | Total Revenue | ||||
1.78M | 0.00 | 0.00 | 125.00K | 125.00K | 125.00K | Gross Profit |
964.00K | 0.00 | -23.98M | -862.00K | -107.00K | 125.00K | EBIT |
-35.55M | -33.37M | -38.39M | -34.72M | -25.73M | -13.81M | EBITDA |
-48.77M | -33.37M | -37.43M | -17.32M | -25.49M | -13.72M | Net Income Common Stockholders |
-52.20M | 0.00 | -37.94M | -2.87M | -36.18M | -22.17M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | ||||
45.06M | 102.65M | 35.41M | 70.06M | 82.64M | 35.05M | Total Assets |
0.00 | 106.87M | 41.20M | 77.69M | 89.20M | 38.28M | Total Debt |
0.00 | 10.87M | 22.76M | 22.80M | 560.00K | 946.00K | Net Debt |
45.06M | -91.79M | -12.65M | -47.26M | -82.08M | -34.11M | Total Liabilities |
0.00 | 40.54M | 28.46M | 29.98M | 25.07M | 61.84M | Stockholders Equity |
41.02M | 66.33M | 12.74M | -99.09M | 64.14M | -23.56M |
Cash Flow | Free Cash Flow | ||||
-28.69M | -27.04M | -34.70M | -32.72M | -24.05M | -10.55M | Operating Cash Flow |
-28.63M | -27.02M | -34.24M | -31.42M | -22.22M | -9.07M | Investing Cash Flow |
-40.00K | -16.00K | -280.00K | -1.30M | -1.83M | 38.45M | Financing Cash Flow |
2.25M | 94.28M | -121.00K | 19.97M | 71.80M | 490.00K |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
54 Neutral | $342.39M | ― | -46.85% | ― | -100.00% | 72.73% | |
49 Neutral | $6.85B | 0.81 | -52.91% | 2.50% | 17.48% | 1.17% | |
42 Neutral | $11.89M | ― | -151.46% | ― | -95.23% | -325.89% | |
41 Neutral | $280.81M | ― | -139.56% | ― | ― | -33.79% | |
34 Underperform | $108.09M | ― | -216.24% | ― | ― | 61.97% | |
20 Underperform | $1.92M | ― | 197.20% | ― | ― | ― |
On March 26, 2025, Candel Therapeutics announced positive final survival data from its phase 2a clinical trial of CAN-2409 in patients with stage III/IV non-small cell lung cancer (NSCLC) who were inadequately responding to immune checkpoint inhibitor (ICI) treatment. The trial results showed a median overall survival (mOS) of 24.5 months for patients with inadequate ICI response and 21.5 months for those with progressive disease, significantly exceeding the survival rates of 9.8–11.8 months reported in similar populations treated with standard chemotherapy. The data also highlighted a potential precision medicine approach, with non-squamous NSCLC patients showing improved survival rates and a systemic anti-tumor response. These findings suggest CAN-2409 may offer a new treatment avenue for NSCLC patients with limited options, and the company plans to advance its development program for this therapy.
On February 25, 2025, Candel Therapeutics announced positive final overall survival data from its phase 2 clinical trial of CAN-2409 in non-metastatic pancreatic cancer. The trial showed that patients treated with CAN-2409 had a median overall survival of 31.4 months compared to 12.5 months in the control group, with a favorable safety profile. This data highlights the potential of CAN-2409 to significantly improve survival in pancreatic cancer, supporting its further development in a larger, late-stage trial.
Candel Therapeutics announced a corporate update highlighting strong pipeline momentum and key value drivers for 2025, including the reporting of updated overall survival data for CAN-2409 in pancreatic ductal adenocarcinoma and non-small cell lung cancer, and preparations for a Biologics License Application for CAN-2409 in prostate cancer. The company reported an unaudited cash position of $102.9 million as of December 31, 2024, sufficient to fund operations into Q1 2027, reflecting their financial stability and capacity to pursue ongoing and upcoming clinical trials and regulatory submissions.