| Breakdown | TTM | Dec 2025 | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 602.20M | 549.32M | 630.20M | 838.00M | 426.41M | 356.13M |
| Gross Profit | 53.76M | 212.48M | 281.32M | 151.55M | 115.31M | 97.89M |
| EBITDA | -7.49M | -41.33M | 14.11M | 67.27M | -401.11M | -321.13M |
| Net Income | 466.88M | 457.58M | 37.73M | 100.78M | -360.83M | -194.65M |
Balance Sheet | ||||||
| Total Assets | 1.78B | 1.75B | 1.27B | 1.28B | 1.03B | 1.37B |
| Cash, Cash Equivalents and Short-Term Investments | 1.36B | 1.37B | 836.11M | 886.34M | 631.00M | 1.01B |
| Total Debt | 93.44M | 97.88M | 89.82M | 86.13M | 27.01M | 38.98M |
| Total Liabilities | 534.02M | 501.77M | 502.34M | 536.39M | 392.57M | 333.15M |
| Stockholders Equity | 1.23B | 1.24B | 759.93M | 730.54M | 610.37M | 986.89M |
Cash Flow | ||||||
| Free Cash Flow | -49.66M | -78.92M | -17.44M | 186.65M | -305.26M | -220.98M |
| Operating Cash Flow | -32.56M | -64.75M | 497.00K | 219.26M | -268.60M | -204.22M |
| Investing Cash Flow | -73.03M | -29.45M | -96.06M | -291.14M | 296.59M | -306.32M |
| Financing Cash Flow | 11.22M | 7.85M | -30.67M | 48.66M | -82.76M | 650.03M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
73 Outperform | HK$25.38B | 6.53 | 12.37% | 3.13% | 10.56% | -13.58% | |
68 Neutral | HK$29.03B | 3.54 | 5.79% | 2.95% | ― | ― | |
66 Neutral | HK$31.62B | 19.33 | 9.90% | 2.26% | 11.78% | 19.06% | |
64 Neutral | HK$21.05B | 3.29 | 20.45% | 5.11% | 0.39% | 4.94% | |
55 Neutral | HK$19.58B | 4.97 | 41.91% | ― | -1.78% | ― | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% |
HUTCHMED (China) Limited has scheduled a board meeting for March 5, 2026 to approve and release its audited financial results for the year ended December 31, 2025, with the announcement to be published that evening in Hong Kong. Following the results release, the company will hold separate English and Putonghua webcast presentations with Q&A for investors and analysts, underscoring its efforts to maintain active investor communication and transparency around its financial performance and strategic direction.
The most recent analyst rating on (HK:0013) stock is a Hold with a HK$25.00 price target. To see the full list of analyst forecasts on HUTCHMED (China) stock, see the HK:0013 Stock Forecast page.
HUTCHMED highlighted the publication in The Lancet of Phase III SACHI trial results, which show that combining its MET inhibitor savolitinib (ORPATHYS®) with AstraZeneca’s osimertinib (TAGRISSO®) significantly improves progression-free survival and response rates versus chemotherapy in patients with advanced EGFR-mutated non-small cell lung cancer who develop MET amplification after prior EGFR-TKI treatment. The data underpin the June 2025 regulatory approval in China for the all-oral savolitinib–osimertinib regimen, reinforcing HUTCHMED’s position in precision oncology and expanding treatment options for a difficult-to-treat subset of lung cancer patients, with a tolerable safety profile and potential to further entrench the company’s role in MET-targeted therapy alongside AstraZeneca.
The most recent analyst rating on (HK:0013) stock is a Hold with a HK$23.00 price target. To see the full list of analyst forecasts on HUTCHMED (China) stock, see the HK:0013 Stock Forecast page.
HUTCHMED announced that the Phase III registration part of its ESLIM-02 trial in China for sovleplenib, an oral spleen tyrosine kinase (Syk) inhibitor, in adults with relapsed or refractory warm antibody autoimmune hemolytic anemia (wAIHA) met its primary endpoint, demonstrating durable hemoglobin responses between weeks 5 and 24. The positive topline data, following earlier Phase II results showing meaningful hemoglobin improvements and a favorable safety profile, underscore sovleplenib’s potential as a new treatment option in wAIHA, a prevalent and often serious form of autoimmune hemolytic anemia with limited therapies after standard treatments fail. HUTCHMED plans to submit a New Drug Application for sovleplenib in wAIHA to China’s National Medical Products Administration in the first half of 2026, while continuing to develop the drug in immune thrombocytopenia, where it has also shown positive Phase III results, reinforcing the company’s positioning in autoimmune hematologic diseases and its strategy to retain global rights to the asset.
The most recent analyst rating on (HK:0013) stock is a Hold with a HK$22.00 price target. To see the full list of analyst forecasts on HUTCHMED (China) stock, see the HK:0013 Stock Forecast page.
HUTCHMED has initiated the Phase III stage of an ongoing Phase II/III clinical trial in China testing a four-drug combination—surufatinib, camrelizumab, nab-paclitaxel and gemcitabine—as a first-line therapy for treatment-naïve patients with metastatic pancreatic ductal adenocarcinoma, a highly lethal cancer with limited effective options. Building on encouraging Phase II data that showed a substantial improvement in progression-free survival, response rates and disease control compared with standard chemotherapy alone, the expansion to approximately 400 additional patients in Phase III underscores the company’s bid to position surufatinib at the core of a potentially new standard treatment regimen in pancreatic cancer and could meaningfully enhance its oncology franchise in the Chinese market if the overall survival endpoint and safety profile remain favorable.
The most recent analyst rating on (HK:0013) stock is a Hold with a HK$22.00 price target. To see the full list of analyst forecasts on HUTCHMED (China) stock, see the HK:0013 Stock Forecast page.
HUTCHMED has initiated a global Phase I clinical development program for HMPL-A251, a first-in-class Antibody-Targeted Therapy Conjugate (ATTC) designed to treat patients with HER2-expressing solid tumors. This trial, conducted in the US and China, marks the first clinical-stage candidate from HUTCHMED’s next-generation ATTC platform, aiming to improve targeted delivery and reduce systemic toxicity. The development of HMPL-A251 could potentially enhance HUTCHMED’s positioning in precision oncology by offering a novel approach to overcoming challenges associated with existing PAM-targeted therapies, thus benefiting stakeholders by expanding treatment options and improving patient outcomes.
The most recent analyst rating on (HK:0013) stock is a Hold with a HK$22.00 price target. To see the full list of analyst forecasts on HUTCHMED (China) stock, see the HK:0013 Stock Forecast page.
HUTCHMED (China) Limited has announced the renewal of its contract with the China National Healthcare Security Administration, ensuring continued inclusion of its drugs ELUNATE®, ORPATHYS®, and SULANDA® in the National Reimbursement Drug List (NRDL) effective January 2023. Additionally, TAZVERIK® has been added to the first edition of the National Commercial Health Insurance Innovative Drug List, which is part of China’s multi-level medical insurance system. This development enhances patient access to innovative treatments and supports the sustainable growth of China’s pharmaceutical sector.
The most recent analyst rating on (HK:0013) stock is a Hold with a HK$22.00 price target. To see the full list of analyst forecasts on HUTCHMED (China) stock, see the HK:0013 Stock Forecast page.