| 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 | ¥307.02B | 11.03 | 9.05% | 3.34% | 10.51% | 9.62% | |
75 Outperform | ¥2.39T | 13.54 | 12.22% | 2.26% | 4.48% | 11.08% | |
74 Outperform | ¥1.27T | 25.80 | 5.75% | 3.49% | 6.79% | 22.14% | |
73 Outperform | ¥310.46B | 15.73 | 7.11% | 2.48% | 3.53% | 38.23% | |
66 Neutral | ¥7.12T | 208.00 | 0.54% | 4.41% | -2.84% | -88.29% | |
66 Neutral | ¥901.06B | 5.85 | 79.99% | ― | 29.92% | ― | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% |
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.
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.
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.
Takeda Pharmaceutical Co. has announced a strategic financial reclassification, reversing general and other voluntary reserves to unappropriated retained earnings. This move, approved by the Board of Directors, aims to enable a more flexible capital policy by utilizing internal reserves accumulated over the years. The reclassification will not impact the company’s consolidated financial results, as it involves adjustments within the net assets section of the balance sheet.
Takeda Pharmaceutical Co has presented promising data from its Phase 3 clinical trials of oveporexton (TAK-861), an investigational oral orexin receptor 2 agonist, at the World Sleep 2025 Congress. The studies demonstrated statistically significant improvements in narcolepsy type 1 symptoms, with no serious treatment-related adverse events reported, marking a potential breakthrough in addressing the underlying cause of this chronic neurological disease.