| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 4.42T | 4.58T | 4.26T | 4.03T | 3.57T | 3.20T |
| Gross Profit | 2.46T | 2.46T | 2.32T | 2.30T | 2.04T | 1.80T |
| EBITDA | 1.14T | 1.13T | 927.95B | 1.18T | 1.04T | 1.07T |
| Net Income | 33.08B | 107.93B | 144.07B | 317.02B | 230.06B | 376.00B |
Balance Sheet | ||||||
| Total Assets | 14.47T | 14.25T | 15.11T | 13.96T | 13.18T | 12.91T |
| Cash, Cash Equivalents and Short-Term Investments | 739.68B | 385.11B | 457.80B | 533.53B | 849.70B | 966.22B |
| Total Debt | 4.65T | 5.09T | 5.46T | 4.86T | 4.81T | 5.07T |
| Total Liabilities | 7.34T | 7.31T | 7.83T | 7.60T | 7.49T | 7.74T |
| Stockholders Equity | 7.13T | 6.94T | 7.27T | 6.35T | 5.68T | 5.17T |
Cash Flow | ||||||
| Free Cash Flow | 931.56B | 761.70B | 464.90B | 736.56B | 897.97B | 793.87B |
| Operating Cash Flow | 1.13T | 962.49B | 640.32B | 877.22B | 1.02T | 905.07B |
| Investing Cash Flow | -230.55B | -385.36B | -488.21B | -615.72B | -204.44B | 392.04B |
| Financing Cash Flow | -1.10T | -638.44B | -254.04B | -600.59B | -962.06B | -981.00B |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
76 Outperform | ¥320.34B | 11.51 | 9.05% | 3.30% | 10.51% | 9.62% | |
75 Outperform | ¥2.56T | 14.48 | 12.22% | 2.22% | 4.48% | 11.08% | |
74 Outperform | ¥1.34T | 27.23 | 5.75% | 3.51% | 6.79% | 22.14% | |
73 Outperform | ¥469.95B | 23.27 | 7.11% | 2.43% | 3.53% | 38.23% | |
66 Neutral | ¥8.05T | 235.34 | 0.54% | 4.11% | -2.84% | -88.29% | |
63 Neutral | ¥1.16T | 7.47 | 79.99% | ― | 29.92% | ― | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% |
Takeda reported positive topline results from two pivotal Phase 3 trials of zasocitinib (TAK-279), a once-daily, highly selective oral TYK2 inhibitor, in adults with moderate-to-severe plaque psoriasis, where the drug met all primary and 44 ranked secondary endpoints and showed superiority to placebo and the active comparator apremilast on key skin clearance measures. More than half of treated patients achieved clear or almost clear skin (PASI 90) and about 30% achieved completely clear skin (PASI 100) by week 16 with a safety profile consistent with prior studies, reinforcing zasocitinib’s potential as a leading oral psoriasis therapy; Takeda plans regulatory submissions starting in fiscal 2026 and is extending development of the drug into psoriatic arthritis, inflammatory bowel disease and other indications, although the Phase 3 results are not expected to affect its current full-year financial forecast.
The most recent analyst rating on (JP:4502) stock is a Hold with a Yen4898.00 price target. To see the full list of analyst forecasts on Takeda Pharmaceutical Co stock, see the JP:4502 Stock Forecast page.
Takeda and Protagonist Therapeutics presented new 52-week data from the Phase 3 VERIFY study at the ASH 2025 meeting, showing rusfertide’s sustained efficacy in controlling hematocrit levels in polycythemia vera patients. The study results reinforce rusfertide’s potential as a new standard of care, demonstrating a significant reduction in phlebotomy needs and maintaining hematocrit control, which is crucial for preventing thrombotic events and alleviating symptoms in patients.
The most recent analyst rating on (JP:4502) stock is a Hold with a Yen4898.00 price target. To see the full list of analyst forecasts on Takeda Pharmaceutical Co stock, see the JP:4502 Stock Forecast page.
Takeda Pharmaceutical Co has revised its financial forecast for the fiscal year ending March 31, 2026, anticipating a decrease in revenue and profits due to factors such as generic erosion of VYVANSE sales in the U.S. and impairment charges. Despite these challenges, the company expects to offset some losses with cost savings from R&D and efficiency programs. The revised outlook reflects a strategic shift towards new product launches and a transition to a new phase of business operations.
The most recent analyst rating on (JP:4502) stock is a Hold with a Yen4500.00 price target. To see the full list of analyst forecasts on Takeda Pharmaceutical Co stock, see the JP:4502 Stock Forecast page.
Takeda Pharmaceutical reported a decline in its financial performance for the six-month period ending September 30, 2025, with significant decreases in revenue, operating profit, and net profit compared to the previous year. Despite the downturn, the company has adjusted its forecasts for the fiscal year ending March 31, 2026, indicating a slight recovery in operating profit and net profit, although core financial measures are expected to see a low-single-digit decline.
The most recent analyst rating on (JP:4502) stock is a Hold with a Yen4500.00 price target. To see the full list of analyst forecasts on Takeda Pharmaceutical Co stock, see the JP:4502 Stock Forecast page.
Takeda Pharmaceutical Co has decided to discontinue its cell therapy research as part of a strategic portfolio prioritization process. The company plans to seek an external partner to advance its cell therapy platform technologies. This decision will result in an impairment loss of approximately JPY 58.0 billion, primarily related to intangible assets associated with the gamma delta T-cell therapy platform. Takeda will redirect its investments towards programs that promise transformative therapies, focusing on small molecules, biologics, and antibody-drug conjugates.
The most recent analyst rating on (JP:4502) stock is a Hold with a Yen4500.00 price target. To see the full list of analyst forecasts on Takeda Pharmaceutical Co stock, see the JP:4502 Stock Forecast page.