Ascentage Pharma Reports 2026 Interim Unaudited Financial Results and Provides Business Updates
Rhea-AI Summary
Ascentage Pharma (NASDAQ: AAPG) reported unaudited results for the six months ended June 30, 2026, with revenue rising 29% year-over-year on a constant currency basis to US$44.5 million (RMB302.2 million), driven by a 32.6% increase in product sales to US$41.6 million. Gross profit reached RMB290.5 million (US$42.8 million).
Operating expenses expanded significantly: selling and distribution expenses grew 64.3% to US$33.4 million, research and development expenses increased 32.0% to US$102.8 million, and administrative expenses rose 19.3% to US$17.5 million. Loss for the period widened to US$120.4 million, or US$0.32 per share. Cash and bank balances were US$279.4 million, down from US$353.2 million at year-end 2025, mainly due to higher R&D spending.
The company highlighted commercial expansion of Olverembatinib and Lisaftoclax in China and progress across nine registrational Phase III trials, plus FDA and China CDE IND clearances for BTK degrader APG-3288. New Chief Business and Chief Commercial Officers were appointed, and the “B” marker was removed from its HKEX short name.
Positive
- Revenue +29.3% YoY to US$44.5 million for H1 2026, driven by product sales growth
- Product sales +32.6% YoY on a constant currency basis to US$41.6 million in H1 2026
- Olverembatinib formulary reach expanded to 879 DTP pharmacies and hospitals, including 394 hospitals, up 34% YoY
- Lisaftoclax market presence at 415 DTP pharmacies and hospitals, including 60 hospitals, as of June 30, 2026
- Nine registrational Phase III trials in progress globally, including FDA- and EMA-cleared POLARIS and GLORA programs
- APG-3288 IND clearances obtained from FDA and China CDE in early 2026, enabling a global Phase I study
- Cash and bank balances of US$279.4 million as of June 30, 2026, providing funding for ongoing trials
Negative
- Net loss widened to US$120.4 million for H1 2026 from US$82.5 million a year earlier
- Loss per share increased to US$0.32 from US$0.24 for the comparable 2025 period
- R&D expenses +32.0% YoY to US$102.8 million, reflecting higher global clinical trial costs
- Selling and distribution expenses +64.3% YoY to US$33.4 million, mainly from increased Lisaftoclax marketing
- Other expenses +71.9% YoY to US$10.2 million, primarily due to higher foreign exchange loss and donations
- Cash and bank balances decreased by US$73.8 million since December 31, 2025, mainly due to accelerated clinical spending
Key Figures
Previous Earnings Reports
| Date | Event | Sentiment | 24h Move | Catalyst |
|---|---|---|---|---|
| Mar 25 | Full-year earnings | Negative | -4.8% | Revenue declined while annual losses and operating investment increased. |
| Aug 20 | Interim earnings | Positive | +1.1% | Product sales growth and Lisaftoclax approval supported the interim update. |
| Mar 27 | Full-year earnings | Positive | +10.0% | Revenue growth, reduced losses, and Nasdaq IPO proceeds strengthened results. |
24h Move is the share-price change in the day after each event; other market factors may also have contributed.
Comparable earnings disclosures produced mixed reactions, ranging from a negative response to strong positive gains.
Key Terms
tki medical
bcr-abl1 medical
pharmacokinetics medical
protac technical
ind clearance regulatory
AI-generated analysis. How Rhea-AI works. Not financial advice.
- Revenue for the first half of 2026 increased
29% year-over-year to US$44.5 million (RMB302.2 million), primarily attributable to increased product sales. - Expanded executive leadership with appointments of Dr. Faical Miyara as Chief Business Officer and Mr. James Ziegler as Chief Commercial Officer
- Nine registrational Phase III clinical trials are in progress worldwide, including four cleared by FDA and EMA
- Chinese (Mandarin) investor webcast at 9:00 am HKT on August 20, 2026 / 9:00 pm EDT on August 19, 2026; and English language investor webcast at 8:00 am EDT / 8:00 pm HKT on August 20, 2026
ROCKVILLE, Md., Aug. 19, 2026 (GLOBE NEWSWIRE) -- Ascentage Pharma Group International (Ascentage Pharma) (NASDAQ: AAPG; HKEX: 6855) (referred hereinto as “Ascentage Pharma,” the “Company,” “we,” “us” or “our”), a global, commercial stage, integrated biopharmaceutical company engaged in the discovery, development and commercialization of novel, differentiated therapies to address unmet medical needs in cancer, today reported its unaudited financial results for the six months ended June 30, 2026, and provided updates on key ongoing clinical programs and commercial activities.
Dr. Dajun Yang, Chairman and Chief Executive Officer of Ascentage Pharma, said, "During the first half of 2026, we continued to execute on our key strategic priorities while expanding our global footprint. The appointments of Dr. Faiçal Miyara as Chief Business Officer and Mr. Jim Ziegler as Chief Commercial Officer further strengthen our strategic capabilities and commercial leadership as we continue building a global commercial-stage oncology company."
Key Commercial Product and Pipeline Updates
Olverembatinib (HQP1351) is a novel, third-generation TKI and the first third-generation BCR-ABL1 TKI approved in China for treatment of patients with chronic myeloid leukemia (CML) in chronic-phase (-CP) or CML in accelerated phase (-AP) with T315I mutations, and in CML-CP that is resistant and/or intolerant to first and second-generation TKIs.
Commercial progress
- The number of Direct-to-Patient (DTP) pharmacies and hospitals where Olverembatinib is on the formulary reached 879 as of June 30, 2026, a
12% increase compared to 782 as of June 30, 2025. In particular, the number of hospitals where Olverembatinib is on the formulary increased by34% over the same period, to 394 hospitals as of June 30, 2026, from 295 hospitals as of June 30, 2025.
Clinical progress
- Enrollment continues in an FDA and EMA-cleared global registrational Phase III clinical trial of Olverembatinib in combination with chemotherapy versus investigator-choice TKI in combination with chemotherapy in patients with newly diagnosed Philadelphia chromosome positive ALL (Ph+ ALL) (POLARIS-1).
- Enrollment continues in an FDA and EMA-cleared global registrational Phase III clinical trial of Olverembatinib for previously treated CML-CP patients, both with and without the T315I mutation (POLARIS-2).
- Enrollment continues in a multinational registrational Phase III clinical trial of Olverembatinib for the treatment of patients with succinate dehydrogenase (SDH)-deficient gastrointestinal stromal tumor (GIST) who have not responded to prior systemic treatment (POLARIS-3).
- Continue to evaluate Olverembatinib in combination with the Bcl-2 inhibitor Lisaftoclax in early-phase clinical trials.
Upcoming milestones
- Continue to advance enrollment in the POLARIS-1, POLARIS-2, and POLARIS-3 trials.
Lisaftoclax (APG-2575) is a novel, oral B-cell lymphoma 2 (Bcl-2) inhibitor developed to treat a variety of hematologic malignancies and solid tumors by selectively blocking Bcl-2 to restore the normal apoptosis process in cancer cells.
Commercial progress
- As of June 30, 2026, the number of DTP pharmacies and hospitals where Lisaftoclax is on the formulary reached 415, including 60 hospitals where Lisaftoclax is on the formulary.
Clinical progress
- Enrollment continues in an FDA and EMA-cleared global, registrational Phase III clinical trial of Lisaftoclax in combination with AZA for the treatment of patients with newly diagnosed HR-MDS (GLORA-4).
- Enrollment continues in a multinational registrational Phase III clinical trial of Lisaftoclax in combination with AZA for the treatment of elderly or unfit patients with newly diagnosed AML (GLORA-3).
- Enrollment continues in a registrational Phase III clinical trial to evaluate Lisaftoclax in combination with the BTK inhibitor acalabrutinib, versus immunochemotherapy in patients with previously untreated CLL/SLL, to investigate a fixed duration of combination regimen as a first-line treatment (GLORA-2).
- Enrollment continues in an FDA and EMA-cleared global registrational Phase III clinical trial of Lisaftoclax in combination with BTK inhibitors in patients with CLL/SLL previously treated sub-optimally with BTK inhibitors (GLORA).
- Enrollment continues in Phase Ib/II clinical trials of Lisaftoclax in combination with other therapies for the treatment of patients with multiple myeloma (MM) in the United States.
- Enrollment continues in a Phase Ib/II study of Lisaftoclax as a single agent or in combination with other therapies for the treatment of patients with AML/MDS, including patients resistant to venetoclax, in China.
- Enrollment continues in Phase Ib/II studies of Lisaftoclax in combination with other therapies for the treatment of patients with AML/MDS in the United States.
Upcoming milestones
- Plan to initiate clinical studies to confirm Lisaftoclax’s potential to overcome venetoclax resistance in patients who have failed venetoclax treatment.
- Continue to advance enrollment in the GLORA, GLORA-2, GLORA-3, and GLORA-4 trials.
- Plan to actively advance the inclusion of Lisaftoclax in China’s NRDL in 2026.
APG-3288 is a novel, highly potent, and selective BTK degrader and first clinical candidate developed utilizing our proprietary proteolysis-targeting chimera (PROTAC) technology platform.
Clinical progress
- Received IND clearance from the FDA in January 2026 and received IND application clearance from the China CDE in February 2026.
- Continue to advance the global Phase I study evaluating APG-3288’s pharmacokinetics, safety, tolerability and efficacy data in patients with relapsed/refractory B-cell malignancies, including in the U.S. and China.
Business Updates
- Appointment of Dr. Faiçal Miyara as Chief Business Officer and Jim Ziegler as Chief Commercial Officer
- Removal of the “B” marker from the HKEX stock short name
Half Year 2026 Unaudited Financial Results
Revenue for the six months ended June 30, 2026 was US
Selling and distribution expenses for the six months ended June 30, 2026 were US
Research and development expenses for the six months ended June 30, 2026 were US
Administrative expenses for the six months ended June 30, 2026 were US
Other expenses for the six months ended June 30, 2026 were US
Loss for the six months ended June 30, 2026 was US
Cash and bank balances as of June 30, 2026, were US
Investor Conference Call and Webcast
Ascentage Pharma will be holding investor webcasts to discuss its six months 2026 unaudited interim results.
Ascentage Pharma will host the Chinese (Mandarin) investor webcast at 9:00 am HKT on August 20, 2026 / 9:00 pm EDT on August 19, 2026. To access the Chinese language investor event or conference call, please register in advance here.
The English language investor webcast will be held at 8:00 am EDT / 8:00 pm HKT on August 20, 2026. To access the English language webcast, please register in advance here. The webcast replay for English language conference call and presentation will also be available on the News & Events page of the Ascentage Pharma website.
Currency and Exchange Rate Information
Unless otherwise indicated, translations from RMB to U.S. dollars for the six months ended June 30, 2026 and 2025 and as at December 31, 2025 are made at RMB6.7851 to US
About Ascentage Pharma
Ascentage Pharma Group International (NASDAQ: AAPG; HKEX: 6855) (“Ascentage Pharma” or the “Company”) is a global, commercial stage, integrated biopharmaceutical company engaged in the discovery, development and commercialization of novel, differentiated therapies to address unmet medical needs in cancer. The Company has built a rich pipeline of innovative drug products and candidates that include inhibitors targeting key proteins in the apoptotic pathway, such as Bcl-2 and MDM2-p53, next-generation kinase inhibitors, and protein degraders.
The Company’s first approved product, Olverembatinib, is the first novel third-generation BCR-ABL1 inhibitor approved in China for the treatment of patients with CML in chronic phase (CML-CP) with T315I mutations, CML in accelerated phase (CML-AP) with T315I mutations, and CML-CP that is resistant or intolerant to first and second-generation TKIs. It is covered by the China National Reimbursement Drug List (NRDL). Ascentage Pharma is currently conducting an FDA- and EMA-cleared registrational Phase III trial, called POLARIS-2, of Olverembatinib for CML, as well as FDA- and EMA-cleared registrational Phase III trials for patients with newly diagnosed Ph+ ALL, called POLARIS-1, and SDH-deficient GIST patients, called POLARIS-3.
The Company’s second approved product, Lisaftoclax, is a novel Bcl-2 inhibitor for the treatment of various hematologic malignancies. Lisaftoclax has been approved by China’s National Medical Products Administration (NMPA) for the treatment of adult patients with chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) who have previously received at least one systemic therapy including Bruton’s tyrosine kinase (BTK) inhibitors. The Company is currently conducting four global registrational Phase III trials: the FDA- and EMA-cleared GLORA study of Lisaftoclax in combination with BTK inhibitors in patients with CLL/SLL previously treated with BTK inhibitors for more than 12 months with suboptimal response; the GLORA-2 study in patients with newly diagnosed CLL/SLL; the GLORA-3 study in newly diagnosed, elderly and unfit patients with AML; and the FDA- and EMA-cleared GLORA-4 study in patients with newly diagnosed higher risk MDS.
Leveraging its robust R&D capabilities, Ascentage Pharma has built a portfolio of global intellectual property rights and entered into global partnerships and other relationships with numerous leading biotechnology and pharmaceutical companies, such as Takeda, AstraZeneca, Merck, Pfizer, and Innovent, in addition to research and development relationships with leading research institutions, such as Dana-Farber Cancer Institute, Mayo Clinic, National Cancer Institute and the University of Michigan. For more information, visit https://ascentage.com/
Cautionary Note Regarding Forward-Looking Statements
This press release includes forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 and Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. All statements, other than statements of historical facts, contained in this press release may be forward-looking statements, including statements that express Ascentage Pharma’s opinions, expectations, beliefs, plans, objectives, assumptions or projections regarding future events or future results of operations or financial condition. These forward-looking statements are subject to a number of risks and uncertainties as discussed in Ascentage Pharma’s filings with the SEC, including those set forth in the sections titled “Risk factors” and “Cautionary note regarding forward-looking statements” in its Annual Report on Form 20-F for the year ended December 31, 2025, filed with the SEC on April 29, 2026, the sections headed “Forward-looking Statements” and “Risk Factors” in the prospectus of the Company for its Hong Kong initial public offering dated October 16, 2019, and other filings with the SEC and/or The Stock Exchange of Hong Kong Limited where the Company’s ordinary shares are listed it has made or it makes from time to time that may cause actual results, levels of activity, performance or achievements to be materially different from the information expressed or implied by these forward-looking statements. The forward-looking statements contained in this press release do not constitute profit forecast by the Company’s management.
As a result of these factors, you should not rely on these forward-looking statements as predictions of future events. The forward-looking statements contained in this press release are based on Ascentage Pharma’s current expectations and beliefs concerning future developments and their potential effects and speak only as of the date of such statements. Ascentage Pharma does not undertake any obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise.
Contact Information
Investor Relations:
Ascentage Pharma
IR@ascentage.com
+1 (301) 792-6286
astr partners
brian.korb@astrpartners.com
+1 (917) 653-5122
| Ascentage Pharma Group International | |||||||||||||||||||||||||
| UNAUDITED INTERIM CONDENSED CONSOLIDATED STATEMENT OF PROFIT OR LOSS | |||||||||||||||||||||||||
| (Amounts in thousands of Renminbi (“RMB”) and U.S. dollar (“US$”), except for number of shares and per share data) | |||||||||||||||||||||||||
| For the Six Months Ended June 30, | |||||||||||||||||||||||||
| 2024 | 2025 | 2026 | 2026 | ||||||||||||||||||||||
| RMB | RMB | RMB | US$ | ||||||||||||||||||||||
| （Unaudited) | （Unaudited) | （Unaudited) | （Unaudited) | ||||||||||||||||||||||
| REVENUE | |||||||||||||||||||||||||
| Intellectual property | 678,416 | - | - | - | |||||||||||||||||||||
| Products | 124,823 | 212,874 | 282,367 | 41,616 | |||||||||||||||||||||
| Others | 20,507 | 20,825 | 19,847 | 2,925 | |||||||||||||||||||||
| Total revenue | 823,746 | 233,699 | 302,214 | 44,541 | |||||||||||||||||||||
| Cost of sales | |||||||||||||||||||||||||
| Products | (14,158 | ) | (20,659 | ) | (10,788 | ) | (1,590 | ) | |||||||||||||||||
| Others | (901 | ) | (991 | ) | (935 | ) | (138 | ) | |||||||||||||||||
| Total cost of sales | (15,059 | ) | (21,650 | ) | (11,723 | ) | (1,728 | ) | |||||||||||||||||
| Gross profit | 808,687 | 212,049 | 290,491 | 42,813 | |||||||||||||||||||||
| Other income and gains | 17,346 | 36,661 | 44,827 | 6,607 | |||||||||||||||||||||
| Selling and distribution expenses | (89,637 | ) | (137,787 | ) | (226,355 | ) | (33,361 | ) | |||||||||||||||||
| Administrative expenses | (86,988 | ) | (99,685 | ) | (118,930 | ) | (17,528 | ) | |||||||||||||||||
| Research and development expenses | (444,079 | ) | (528,561 | ) | (697,460 | ) | (102,793 | ) | |||||||||||||||||
| Other expenses | (7,106 | ) | (40,192 | ) | (69,110 | ) | (10,186 | ) | |||||||||||||||||
| Finance costs | (34,076 | ) | (27,798 | ) | (26,814 | ) | (3,952 | ) | |||||||||||||||||
| Share of (loss)/profit of a joint venture | (1,252 | ) | 1 | (22 | ) | (3 | ) | ||||||||||||||||||
| PROFIT/(LOSS) BEFORE TAX | 162,895 | (585,312 | ) | (803,373 | ) | (118,403 | ) | ||||||||||||||||||
| Income tax expense | (69 | ) | (5,512 | ) | (13,625 | ) | (2,008 | ) | |||||||||||||||||
| PROFIT/(LOSS) FOR THE PERIOD | 162,826 | (590,824 | ) | (816,998 | ) | (120,411 | ) | ||||||||||||||||||
| Attributable to: | |||||||||||||||||||||||||
| Ordinary equity holders of the Company | 163,001 | (590,768 | ) | (816,694 | ) | (120,366 | ) | ||||||||||||||||||
| Non-controlling interests | (175 | ) | (56 | ) | (304 | ) | (45 | ) | |||||||||||||||||
| 162,826 | (590,824 | ) | (816,998 | ) | (120,411 | ) | |||||||||||||||||||
| EARNINGS/(LOSS) PER SHARE ATTRIBUTABLE TO ORDINARY EQUITY HOLDERS OF THE COMPANY | |||||||||||||||||||||||||
| Basic | 0.56 | (1.73 | ) | (2.19 | ) | (0.32 | ) | ||||||||||||||||||
| Diluted | 0.55 | (1.73 | ) | (2.19 | ) | (0.32 | ) | ||||||||||||||||||
| Ascentage Pharma Group International | ||||||||||||||||||||
| UNAUDITED INTERIM CONDENSED CONSOLIDATED STATEMENT OF COMPREHENSIVE LOSS | ||||||||||||||||||||
| (Amounts in thousands of Renminbi (“RMB”) and U.S. dollar (“US$”), except for number of shares and per share data) | ||||||||||||||||||||
| For the Six Months Ended June 30, | ||||||||||||||||||||
| 2024 | 2025 | 2026 | 2026 | |||||||||||||||||
| RMB | RMB | RMB | US$ | |||||||||||||||||
| （Unaudited) | （Unaudited) | （Unaudited) | （Unaudited) | |||||||||||||||||
| PROFIT/(LOSS) FOR THE PERIOD | 162,826 | (590,824 | ) | (816,998 | ) | (120,411 | ) | |||||||||||||
| OTHER COMPREHENSIVE INCOME/(LOSS) | ||||||||||||||||||||
| Other comprehensive income that may be reclassified to profit or loss in subsequent periods: | ||||||||||||||||||||
| Exchange differences on translation of foreign operations | 40 | 1,095 | 29,078 | 4,285 | ||||||||||||||||
| Other comprehensive income that will not be reclassified to profit or loss in subsequent periods, net of tax: | ||||||||||||||||||||
| Exchange differences on translation of the Company | 2,229 | (2,035 | ) | (57,207 | ) | (8,431 | ) | |||||||||||||
| OTHER COMPREHENSIVE INCOME/(LOSS) FOR THE PERIOD, NET OF TAX | 2,269 | (940 | ) | (28,129 | ) | (4,146 | ) | |||||||||||||
| TOTAL COMPREHENSIVE INCOME/(LOSS) FOR THE PERIOD | 165,095 | (591,764 | ) | (845,127 | ) | (124,557 | ) | |||||||||||||
| Attributable to: | ||||||||||||||||||||
| Ordinary equity holders of the Company | 165,270 | (591,708 | ) | (844,823 | ) | (124,512 | ) | |||||||||||||
| Non-controlling interests | (175 | ) | (56 | ) | (304 | ) | (45 | ) | ||||||||||||
| 165,095 | (591,764 | ) | (845,127 | ) | (124,557 | ) | ||||||||||||||
| Ascentage Pharma Group International | |||||||||||||||||
| UNAUDITED INTERIM CONDENSED CONSOLIDATED STATEMENT OF FINANCIAL POSITION | |||||||||||||||||
| (Amounts in thousands of Renminbi (“RMB”) and U.S. dollar (“US$”), except for number of shares and per share data) | |||||||||||||||||
| As at | |||||||||||||||||
| December 31, 2025 | June 30, 2026 | June 30, 2026 | |||||||||||||||
| RMB | RMB | US$ | |||||||||||||||
| （Unaudited) | （Unaudited) | ||||||||||||||||
| NON-CURRENT ASSETS | |||||||||||||||||
| Property, plant and equipment | 781,235 | 751,518 | 110,760 | ||||||||||||||
| Right-of-use assets | 47,827 | 48,915 | 7,209 | ||||||||||||||
| Goodwill | 24,694 | 24,694 | 3,639 | ||||||||||||||
| Other intangible assets | 65,936 | 37,566 | 5,537 | ||||||||||||||
| Investment in a joint venture | 33,030 | 33,009 | 4,865 | ||||||||||||||
| Financial assets at fair value through profit or loss (“FVTPL”) | 4,000 | 7,000 | 1,032 | ||||||||||||||
| Deferred tax assets | 31,957 | 18,375 | 2,708 | ||||||||||||||
| Other non-current assets | 30,725 | 26,361 | 3,885 | ||||||||||||||
| Total non-current assets | 1,019,404 | 947,438 | 139,635 | ||||||||||||||
| CURRENT ASSETS | |||||||||||||||||
| Inventories | 28,618 | 64,300 | 9,477 | ||||||||||||||
| Trade receivables, net | 252,938 | 156,396 | 23,050 | ||||||||||||||
| Prepayments, other receivables and other assets | 192,532 | 176,985 | 26,084 | ||||||||||||||
| Cash and bank balances | 2,470,085 | 1,895,583 | 279,374 | ||||||||||||||
| Total current assets | 2,944,173 | 2,293,264 | 337,985 | ||||||||||||||
| CURRENT LIABILITIES | |||||||||||||||||
| Trade payables | 106,740 | 106,912 | 15,756 | ||||||||||||||
| Other payables and accruals | 276,666 | 231,932 | 34,183 | ||||||||||||||
| Contract liabilities | 37,485 | 69,539 | 10,249 | ||||||||||||||
| Interest-bearing bank and other borrowings | 1,222,481 | 1,475,122 | 217,406 | ||||||||||||||
| Total current liabilities | 1,643,372 | 1,883,505 | 277,594 | ||||||||||||||
| NET CURRENT ASSETS | 1,300,801 | 409,759 | 60,391 | ||||||||||||||
| TOTAL ASSETS LESS CURRENT LIABILITIES | 2,320,205 | 1,357,197 | 200,026 | ||||||||||||||
| Ascentage Pharma Group International | ||||||||||||||||||||||||
| UNAUDITED INTERIM CONDENSED CONSOLIDATED STATEMENT OF FINANCIAL POSITION | ||||||||||||||||||||||||
| (Amounts in thousands of Renminbi (“RMB”) and U.S. dollar (“US$”), except for number of shares and per share data) | ||||||||||||||||||||||||
| As at | ||||||||||||||||||||||||
| December 31, 2025 | June 30, 2026 | June 30, 2026 | ||||||||||||||||||||||
| RMB | RMB | US$ | ||||||||||||||||||||||
| （Unaudited) | （Unaudited) | |||||||||||||||||||||||
| NON-CURRENT LIABILITIES | ||||||||||||||||||||||||
| Contract liabilities | 210,224 | 158,453 | 23,353 | |||||||||||||||||||||
| Interest-bearing bank and other borrowings | 757,238 | 619,449 | 91,295 | |||||||||||||||||||||
| Deferred income | 6,500 | 6,300 | 929 | |||||||||||||||||||||
| Other non-current liabilities | 12,031 | 7,162 | 1,056 | |||||||||||||||||||||
| Total non-current liabilities | 985,993 | 791,364 | 116,633 | |||||||||||||||||||||
| TOTAL LIABILITIES | 2,629,365 | 2,674,869 | 394,227 | |||||||||||||||||||||
| EQUITY | ||||||||||||||||||||||||
| Equity attributable to ordinary equity holders of the Company | ||||||||||||||||||||||||
| Ordinary shares (par value of US | 256 | 256 | 38 | |||||||||||||||||||||
| Treasury shares | (2,961 | ) | (16,362 | ) | (2,411 | ) | ||||||||||||||||||
| Share premium | 8,916,853 | 8,926,700 | 1,315,632 | |||||||||||||||||||||
| Capital and reserves | (397,276 | ) | (316,974 | ) | (46,716 | ) | ||||||||||||||||||
| Exchange fluctuation reserve | (179,086 | ) | (207,215 | ) | (30,540 | ) | ||||||||||||||||||
| Accumulated losses | (7,013,324 | ) | (7,830,018 | ) | (1,154,002 | ) | ||||||||||||||||||
| 1,324,462 | 556,387 | 82,001 | ||||||||||||||||||||||
| Non-controlling interests | 9,750 | 9,446 | 1,392 | |||||||||||||||||||||
| Total equity | 1,334,212 | 565,833 | 83,393 | |||||||||||||||||||||
