| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 618.84M | 503.99M | 19.06M | 0.00 | 22.68M | 0.00 |
| Gross Profit | 618.84M | 503.99M | 19.06M | 0.00 | 22.68M | 0.00 |
| EBITDA | 96.28M | -15.28M | -410.99M | -492.62M | -1.80B | -150.21M |
| Net Income | 149.98M | 28.30M | -431.58M | -498.29M | -1.81B | -706.81M |
Balance Sheet | ||||||
| Total Assets | 2.44B | 2.11B | 2.12B | 2.49B | 2.65B | 665.97M |
| Cash, Cash Equivalents and Short-Term Investments | 2.38B | 2.01B | 1.96B | 2.35B | 2.57B | 636.66M |
| Total Debt | 17.77M | 24.29M | 35.72M | 45.58M | 53.80M | 4.31M |
| Total Liabilities | 217.96M | 148.71M | 134.28M | 143.16M | 118.48M | 1.77B |
| Stockholders Equity | 2.22B | 1.96B | 1.98B | 2.35B | 2.54B | -1.10B |
Cash Flow | ||||||
| Free Cash Flow | 126.03M | -20.32M | -456.98M | -366.64M | -182.08M | -121.60M |
| Operating Cash Flow | 129.00M | -12.92M | -444.73M | -343.90M | -169.74M | -117.56M |
| Investing Cash Flow | 239.41M | -196.50M | 378.52M | -216.57M | -1.46B | -11.25M |
| Financing Cash Flow | 23.09M | -80.86M | -16.11M | -20.81M | 2.10B | 505.89M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
57 Neutral | HK$9.20B | 47.27 | 6.73% | ― | 23.37% | ― | |
54 Neutral | HK$13.12B | -44.32 | -12.74% | ― | -76.58% | -4.90% | |
53 Neutral | HK$9.97B | 40.68 | 13.34% | ― | 206.58% | ― | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
51 Neutral | HK$11.34B | 16.93 | 35.80% | ― | 59.70% | 239.97% | |
42 Neutral | HK$8.17B | -18.58 | -95.84% | ― | -55.64% | -158.67% |
Abbisko Cayman Limited announced that its subsidiary, Abbisko Therapeutics, has received clearance from the U.S. FDA for its Investigational New Drug application for ABSK141, a novel oral small-molecule KRAS G12D inhibitor. This development marks a significant step in addressing the challenging KRAS G12D mutation found in various solid tumors, including pancreatic, colorectal, and non-small cell lung cancers. The IND clearance allows Abbisko to proceed with Phase I/II clinical trials to evaluate the drug’s safety and efficacy, potentially strengthening its position in the oncology pharmaceutical industry.
Abbisko Therapeutics, a subsidiary of Abbisko Cayman Limited, presented promising long-term efficacy and safety results from its Phase III MANEUVER study of pimicotinib at the CTOS 2025 Annual Meeting. The study demonstrated significant improvements in tumor response and patient quality of life, reinforcing pimicotinib’s potential for long-term use in TGCT patients. The results highlight the drug’s robust and durable response, with a notable increase in objective response rate and quality of life improvements over time, positioning Abbisko as a key player in the TGCT treatment landscape.
Abbisko Cayman Limited announced that its subsidiary, Abbisko Therapeutics, has completed the first patient dosing in a Phase II clinical study of ABSK043, an oral small-molecule PD-L1 inhibitor, in combination with Glecirasib for treating non-small cell lung cancer (NSCLC) with KRAS G12C mutation. This milestone marks a significant advancement in the development of this treatment regimen, which aims to address a prevalent oncogenic driver in human cancer. The study, approved by China’s National Medical Products Administration, seeks to evaluate the safety and efficacy of this novel combination therapy, potentially impacting the company’s market positioning and offering new hope for patients with advanced NSCLC.
Abbisko Therapeutics announced promising preclinical findings for two of its drug candidates, the CDK4/2 inhibitor ABK-CDK-1 and the SMARCA2 PROTAC degrader ABK-SM2-1, at the 37th AACR-NCI-EORTC Conference. These developments highlight the company’s efforts to overcome limitations of existing cancer treatments, potentially enhancing its positioning in the oncology sector and offering new therapeutic options for patients.
Abbisko Cayman Limited announced promising longer-term efficacy and safety outcomes from its Phase III MANEUVER trial of pimicotinib, a CSF-1R inhibitor, for treating tenosynovial giant cell tumour (TGCT). Presented at ESMO 2025, the results showed significant and durable tumor response improvements, with a favorable safety profile, suggesting pimicotinib’s potential as a leading therapy in TGCT management. These findings enhance the drug’s commercial prospects and Abbisko’s position in the oncology market.
Abbisko Cayman Limited has announced the grant of 6,343,508 share options to three directors and certain employees under its Post-IPO Share Option Scheme. The options are subject to performance targets at both group and individual levels, with vesting scheduled over four years. This move aims to align the interests of the company’s leadership and employees with its strategic goals, potentially enhancing its competitive positioning in the pharmaceutical industry.