| 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 |
|---|---|---|---|---|---|---|---|
60 Neutral | $708.06M | -1.45 | -75.75% | ― | -34.92% | -43.26% | |
56 Neutral | $300.88M | -3.81 | ― | ― | ― | ― | |
54 Neutral | $314.95M | -13.11 | -31.07% | ― | 158.54% | 66.90% | |
53 Neutral | $385.89M | -9.68 | -35.86% | ― | ― | -17.16% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
46 Neutral | $187.75M | -0.14 | ― | ― | ― | ― | |
45 Neutral | ― | ― | ― | ― | -100.00% | 72.45% |
On December 8, 2025, Immutep Limited announced a strategic collaboration with Dr. Reddy’s Laboratories for the commercialization of its innovative oncology drug, Eftilagimod Alfa (efti), outside North America, Europe, Japan, and Greater China. This agreement grants Dr. Reddy’s exclusive rights to develop and commercialize efti in these regions, with Immutep receiving an upfront payment of USD 20 million and potential milestone payments of up to USD 349.5 million, along with double-digit royalties on sales. The partnership is expected to enhance Immutep’s market presence and validate the potential of efti, which is currently under evaluation in a Phase III trial for non-small cell lung cancer and other cancer types.
Immutep Limited announced that it will present new data from its AIPAC-003 Phase II trial at the 2025 San Antonio Breast Cancer Symposium. The trial, which involved heavily pretreated metastatic breast cancer patients, demonstrated strong objective response and disease control rates with the combination of eftilagimod alfa (efti) and paclitaxel. The study successfully met the FDA’s Project Optimus requirements, establishing 30 mg as the optimal biological dose for efti. This development is strategically important for Immutep’s ongoing and future clinical programs, including its global TACTI-004 Phase III trial in non-small cell lung cancer.
Immutep Limited announced positive results from the EFTISARC-NEO Phase II trial, presented at the CTOS 2025 Annual Meeting. The trial, which involved a novel combination of eftilagimod alfa (efti) with radiotherapy and KEYTRUDA® for resectable soft tissue sarcoma, showed significant tumor hyalinization/fibrosis and strong immune activation. These findings suggest potential for improved patient outcomes and survival rates, highlighting efti’s role in enhancing immune response against cancer. The promising data supports further investigation into efti’s use in earlier-stage cancers, potentially expanding its application to patients with lower tumor burdens.
On November 3, 2025, Immutep Limited announced it received a €2,588,954 (~ A$4,567,769) R&D tax incentive from the French Government under the Crédit d’Impôt Recherche scheme. This incentive supports the company’s research and development activities conducted in Europe during the 2024 calendar year. The funds will be used to further the global clinical development of eftilagimod alfa and IMP761, enhancing Immutep’s position in the immunotherapy sector.
Immutep Limited has released its quarterly activities report for Q1 FY26, highlighting significant progress in its clinical trials and financial position. The company is advancing its pivotal TACTI-004 Phase III trial for eftilagimod alfa in non-small cell lung cancer, with over 100 clinical sites now open for enrollment across 24 countries. Additionally, Immutep received positive feedback from the FDA for its head and neck cancer program and launched a new Phase II trial for breast cancer. The company maintains a strong financial position with A$109.85 million in cash, ensuring operations through the end of 2026.
On October 20, 2025, Immutep Limited presented two posters at the ESMO Congress 2025, showcasing promising results from the INSIGHT-003 trial. The trial demonstrated that the combination of eftilagimod alfa (efti) with KEYTRUDA and chemotherapy significantly improved response rates in first-line non-small cell lung cancer (1L NSCLC) patients, particularly those with low or no PD-L1 expression. This advancement could potentially redefine the treatment paradigm for 1L NSCLC, offering new hope for patients with high unmet needs. The company is also progressing with its pivotal TACTI-004 Phase III trial, which aims to further validate efti’s efficacy and safety in a larger patient population.
Immutep Limited announced positive results from its EFTISARC-NEO Phase II trial, which evaluated the use of eftilagimod alfa (efti) in combination with radiotherapy and KEYTRUDA® for treating resectable soft tissue sarcoma (STS). The trial, presented at the 2025 European Society of Medical Oncology Congress, demonstrated a significant improvement in tumor hyalinization/fibrosis, achieving a median of 51.5% compared to 15% from standard radiotherapy alone. This outcome suggests potential for better patient outcomes, addressing the high unmet medical need in STS treatment.
Immutep Limited announced on October 13, 2025, the successful completion of the FDA’s Project Optimus requirements, confirming 30mg as the optimal biological dose for its immunotherapy candidate eftilagimod alfa (efti). This milestone is strategically significant for Immutep’s oncology programs and paves the way for future Biological License Applications. The completion of Project Optimus also facilitates the opening of clinical sites in the United States for the TACTI-004 (KEYNOTE-F91) Phase III trial, which evaluates efti in combination with MSD’s KEYTRUDA® and chemotherapy for first-line treatment of advanced non-small cell lung cancer.
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.