Breakdown | TTM | Dec 2025 | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 |
---|---|---|---|---|---|---|
Income Statement | ||||||
Total Revenue | 5.04M | 5.04M | 3.84M | 3.51M | 170.37K | 3.86M |
Gross Profit | -56.37M | -56.37M | -37.70M | 1.44M | -1.89M | -13.37M |
EBITDA | -62.88M | -62.88M | -44.54M | -39.57M | -31.87M | -17.77M |
Net Income | -61.43M | -61.43M | -42.72M | -39.90M | -32.21M | -29.90M |
Balance Sheet | ||||||
Total Assets | 156.98M | 156.98M | 201.58M | 147.45M | 102.17M | 82.03M |
Cash, Cash Equivalents and Short-Term Investments | 129.69M | 129.69M | 181.88M | 123.42M | 80.00M | 60.13M |
Total Debt | 1.63M | 1.63M | 1.59M | 1.23M | 1.73M | 2.82M |
Total Liabilities | 13.35M | 13.35M | 12.06M | 10.98M | 8.09M | 8.76M |
Stockholders Equity | 143.64M | 143.64M | 189.52M | 136.47M | 94.08M | 73.27M |
Cash Flow | ||||||
Free Cash Flow | -62.10M | -62.10M | -35.75M | -35.93M | -30.25M | -17.66M |
Operating Cash Flow | -62.05M | -62.05M | -34.82M | -35.88M | -30.23M | -17.64M |
Investing Cash Flow | -6.12M | -38.53M | -21.02M | -31.00K | -22.91K | -15.60K |
Financing Cash Flow | -152.12K | -525.12K | 95.18M | 76.04M | 50.33M | 52.68M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
64 Neutral | $323.56M | ― | -48.36% | ― | 334.02% | ― | |
54 Neutral | $350.80M | ― | -76.59% | ― | 11.11% | -46.50% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
51 Neutral | $280.35M | ― | -35.86% | ― | ― | -17.16% | |
46 Neutral | $247.98M | ― | -99.23% | ― | ― | ― | |
45 Neutral | $401.51M | ― | -22.44% | ― | -100.00% | 72.45% | |
44 Neutral | $266.00M | ― | -938.38% | ― | ― | ― |
On September 22, 2025, Immutep announced a research collaboration with the George Washington University Cancer Center to initiate a Phase II trial evaluating its immunotherapy drug, eftilagimod alfa (efti), in early-stage HR+/HER2-negative breast cancer patients. The trial will explore efti as a monotherapy and in combination with chemotherapy, aiming to enhance the anti-cancer immune response and improve pathologic complete response rates. This collaboration marks a strategic expansion of Immutep’s clinical pipeline, potentially strengthening its position in the immunotherapy market and addressing high unmet medical needs.
Immutep Limited reported its preliminary financial results for the year ended June 30, 2025, on August 29, 2025. The company experienced an increase in losses, with a loss after tax rising from $42.7 million in FY2024 to $61.4 million in FY2025. This increase was primarily due to a $19.9 million rise in R&D and intellectual property expenses, largely driven by higher clinical trial costs. Despite the financial loss, the company saw a rise in other income and interest income, attributed to higher cash balances invested in term deposits. The report highlights the company’s ongoing commitment to advancing its clinical trials, although it did not declare any dividends for the period.
On August 5, 2025, Immutep Limited announced that it received positive feedback from the FDA regarding the clinical development of its MHC Class II agonist, eftilagimod alfa, for treating recurrent/metastatic head and neck squamous cell carcinoma patients with low PD-L1 expression. The FDA’s support highlights the potential of eftilagimod alfa in combination with KEYTRUDA to address unmet medical needs in this patient segment, paving the way for future clinical trials and potential accelerated approval. This feedback positions Immutep to explore collaborative development paths, potentially enhancing its market position and offering new treatment options for underserved patients.
Immutep Limited has announced significant progress in its clinical trials and research activities for the quarter ending June 30, 2025. The company is advancing its TACTI-004 Phase III trial for non-small cell lung cancer, with patient recruitment expanding across 78 sites in 23 countries. The INSIGHT-003 trial showed promising results with a high response rate in lung cancer patients, while the EFTISARC-NEO trial in soft tissue sarcoma met its primary endpoint. Additionally, the company reported positive initial data from its IMP761 Phase I trial for autoimmune diseases, highlighting its potential efficacy. Immutep maintains a strong cash position, supporting its operations through the end of 2026.