Breakdown | ||||
Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|
Income Statement | Total Revenue | |||
0.00 | 0.00 | 125.00K | 125.00K | 125.00K | Gross Profit |
0.00 | -23.98M | -862.00K | -107.00K | 125.00K | EBIT |
-33.37M | -38.39M | -34.72M | -25.73M | -13.81M | EBITDA |
-33.37M | -37.43M | -17.32M | -25.49M | -13.72M | Net Income Common Stockholders |
0.00 | -37.94M | -2.87M | -36.18M | -22.17M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | |||
102.65M | 35.41M | 70.06M | 82.64M | 35.05M | Total Assets |
106.87M | 41.20M | 77.69M | 89.20M | 38.28M | Total Debt |
10.87M | 22.76M | 22.80M | 560.00K | 946.00K | Net Debt |
-91.79M | -12.65M | -47.26M | -82.08M | -34.11M | Total Liabilities |
40.54M | 28.46M | 29.98M | 25.07M | 61.84M | Stockholders Equity |
66.33M | 12.74M | -99.09M | 64.14M | -23.56M |
Cash Flow | Free Cash Flow | |||
-27.04M | -34.70M | -32.72M | -24.05M | -10.55M | Operating Cash Flow |
-27.02M | -34.24M | -31.42M | -22.22M | -9.07M | Investing Cash Flow |
-16.00K | -280.00K | -1.30M | -1.83M | 38.45M | Financing Cash Flow |
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 |
---|---|---|---|---|---|---|---|
73 Outperform | $652.30M | 12.72 | 50.22% | ― | 93.80% | ― | |
60 Neutral | $251.67M | ― | -36.07% | ― | ― | -7.93% | |
52 Neutral | $5.28B | 3.75 | -42.72% | 2.86% | 17.70% | 2.03% | |
50 Neutral | $341.38M | ― | 344.74% | ― | -47.32% | -26.67% | |
48 Neutral | $296.79M | ― | -79.69% | ― | -33.43% | 8.94% | |
46 Neutral | $352.74M | ― | -39.07% | ― | ― | 0.42% | |
33 Underperform | $230.98M | ― | -139.56% | ― | ― | -33.79% |
On April 23, 2025, Candel Therapeutics announced that an abstract featuring positive results from their phase 3 clinical trial of CAN-2409 in localized prostate cancer was accepted for oral presentation at the 2025 ASCO Annual Meeting. The trial demonstrated significant improvement in disease-free survival when CAN-2409 was added to standard-of-care radiation therapy, highlighting its potential impact on cancer treatment and Candel’s positioning in the biopharmaceutical industry.
Spark’s Take on CADL Stock
According to Spark, TipRanks’ AI Analyst, CADL is a Underperform.
Candel Therapeutics faces substantial financial hurdles with no revenue and ongoing cash burn. While recent positive trial results provide some hope for future growth and development, the technical analysis and valuation remain negative. The stock is highly speculative, with potential upsides hinging on the success of pipeline developments and financial stabilization.
To see Spark’s full report on CADL stock, click here.
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.