| Breakdown | Dec 2025 | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 |
|---|---|---|---|---|---|
Income Statement | |||||
| Total Revenue | 48.27M | 155.84M | 54.00M | 172.83M | 34.76M |
| Gross Profit | 48.27M | 155.84M | -64.67M | 66.05M | -52.81M |
| EBITDA | -167.47M | 34.46M | -88.93M | 50.04M | -87.30M |
| Net Income | -188.69M | 15.22M | -96.99M | 37.51M | -95.06M |
Balance Sheet | |||||
| Total Assets | 562.10M | 696.15M | 509.96M | 407.82M | 174.65M |
| Cash, Cash Equivalents and Short-Term Investments | 469.14M | 604.45M | 425.89M | 362.20M | 145.12M |
| Total Debt | 15.63M | 16.20M | 15.40M | 14.56M | 9.85M |
| Total Liabilities | 78.20M | 121.30M | 284.88M | 194.66M | 150.58M |
| Stockholders Equity | 483.89M | 574.84M | 225.08M | 213.16M | 24.06M |
Cash Flow | |||||
| Free Cash Flow | -175.95M | -174.51M | -12.73M | 93.92M | -87.44M |
| Operating Cash Flow | -169.66M | -158.03M | 18.23M | 100.13M | -81.78M |
| Investing Cash Flow | 196.70M | -152.39M | -31.39M | -209.79M | 7.49M |
| Financing Cash Flow | 93.51M | 319.68M | 84.52M | 123.71M | -2.61M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
59 Neutral | $1.77B | ― | -43.17% | ― | -16.50% | 33.02% | |
57 Neutral | $992.84M | -10.26 | -34.23% | ― | 522.13% | 62.68% | |
55 Neutral | $2.67B | -10.13 | -50.30% | ― | 53.28% | 21.77% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
51 Neutral | $1.30B | ― | -39.69% | ― | -27.61% | -69.49% | |
50 Neutral | $2.33B | -8.83 | -57.61% | ― | -4.44% | 63.58% | |
46 Neutral | $835.29M | -4.22 | -141.99% | ― | ― | 31.16% |
On March 5, 2026, Immatics reported its full-year 2025 results and outlined progress across its PRAME-franchise programs, led by anzu-cel, which is in the global Phase 3 SUPRAME trial for previously treated advanced cutaneous melanoma and holds U.S. Orphan Drug and RMAT designations in cutaneous and uveal melanoma. The company confirmed timelines for interim and final SUPRAME analyses in 2026, a planned BLA filing in the first half of 2027 and a potential commercial launch in the second half of 2027, supported by ongoing Phase 1/2 melanoma studies, a Moderna-backed combination trial, advancing next-generation IMA203CD8 and IMA402 bispecific programs, and a strengthened balance sheet with $551.4 million in cash and equivalents after a $125 million offering, extending its cash runway into 2028.
Immatics also highlighted positive early data for IMA203CD8 in PRAME-positive tumors, including ovarian cancer, and laid out 2026 data catalysts for this second-generation cell therapy and for its IMA402 PRAME bispecific, which is moving toward indication-specific expansion cohorts and a planned combination trial with IMA401 in squamous non-small cell lung cancer. Taken together, the clinical momentum, regulatory designations and extended funding horizon reinforce Immatics’ bid to establish a first-to-market position in PRAME-targeted therapies while broadening its addressable patient population in solid tumors.
The most recent analyst rating on (IMTX) stock is a Buy with a $25.00 price target. To see the full list of analyst forecasts on Immatics stock, see the IMTX Stock Forecast page.
On January 12, 2026, Immatics N.V. filed a report with U.S. securities regulators announcing that it had posted an updated corporate investor presentation on its website, formally placing the materials in the public domain. The presentation highlights the company’s expanding pipeline of PRAME‑targeted product candidates, including the TCR‑T cell therapy anzutresgene autoleucel (anzu‑cel, formerly IMA203), its second‑generation IMA203CD8, and the bispecific antibody IMA402, which are being advanced across multiple solid tumor indications and stages of development from Phase 1 through preclinical. By emphasizing its leadership in precision PRAME targeting and outlining a multi‑modality development strategy in melanoma, gynecologic cancers and other solid tumors, Immatics is signaling to investors and partners its intent to consolidate a competitive position in next‑generation cancer immunotherapy, although the company stresses that the information is current only as of the presentation date and may be subject to future change.
The most recent analyst rating on (IMTX) stock is a Buy with a $17.00 price target. To see the full list of analyst forecasts on Immatics stock, see the IMTX Stock Forecast page.
On December 11, 2025, Immatics announced updated results from its Phase 1a clinical trial of the IMA203CD8 PRAME cell therapy, which targets heavily pre-treated patients with solid tumors. The data, with a cutoff date of October 27, 2025, revealed that the therapy demonstrated manageable tolerability and promising anti-tumor activity, with a confirmed objective response rate of 36% and a disease control rate of 84% at week 6. The trial’s ongoing dose escalation aims to determine the recommended Phase 2 dose in 2026, potentially positioning IMA203CD8 in a tumor-agnostic setting beyond melanoma, particularly in gynecologic cancers. This development could enhance Immatics’ standing in the biopharmaceutical industry by expanding its therapeutic offerings across a broader spectrum of PRAME-expressing cancers.
The most recent analyst rating on (IMTX) stock is a Buy with a $23.00 price target. To see the full list of analyst forecasts on Immatics stock, see the IMTX Stock Forecast page.
On December 8, 2025, Immatics N.V. completed an offering of 12,500,000 ordinary shares, raising approximately $116.5 million after expenses. The proceeds will support the company’s research and development pipeline, manufacturing, and potential commercialization of its product candidates. This strategic move is expected to bolster Immatics’ position in the biopharmaceutical industry, enhancing its operational capabilities and market presence.
The most recent analyst rating on (IMTX) stock is a Buy with a $23.00 price target. To see the full list of analyst forecasts on Immatics stock, see the IMTX Stock Forecast page.