ASCENTAGE (06855.HK): Interim Revenue Up 29.3% to RMB 302.2 Million, Net Loss Widens to RMB 817.0 Million
- Gross profit was RMB 290.5 million, with product sales rising 32.6% year on year to RMB 282.4 million.
- Research and development expenses were RMB 697.5 million and selling and distribution expenses RMB 226.4 million, up 32.0% and 64.3% respectively year on year.
- Net cash used in operating activities was RMB 581.2 million, and total equity decreased to RMB 565.8 million from RMB 1,334.2 million.
NewTimeSpace News: On 17 September 2026, Ascentage Pharma Group International (stock code: 06855) published its 2026 interim report. Revenue for the six months ended 30 June 2026 was RMB 302.2 million, up 29.3% year on year on a constant exchange rate basis, driven by a 32.6% increase in product sales to RMB 282.4 million. Net loss for the period was RMB 817.0 million, compared with a loss of RMB 590.8 million a year earlier, and basic and diluted loss per share was RMB 2.19.
Total operating expenses rose 36.1% to RMB 1,042.7 million, of which research and development expenses increased 32.0% to RMB 697.5 million, mainly due to progress in the Group's ongoing global clinical trials, while selling and distribution expenses rose 64.3% to RMB 226.4 million, mainly attributable to increased marketing and promotion investment in Lisaftoclax.
As at 30 June 2026, the Group's cash and bank balances were RMB 1,895.6 million, down 23.3% from 31 December 2025, mainly due to ongoing operating expenses related to global clinical trials and research and development. No fundraising activities were carried out during the reporting period; the current ratio fell to 1.2 from 1.8 and the gearing ratio rose to 35.8%.
With effect from 1 June 2026, the Company removed the "B" marker from its Chinese and English stock short names, having met the market capitalisation/revenue test under Rule 8.05(3) of the Listing Rules and been granted relief from Rules 18A.09 to 18A.11. Its BTK-targeted protein degrader APG-3288 obtained investigational new drug clearance from the US FDA in January 2026 and from the CDE of China's National Medical Products Administration in February 2026, and a Phase I study in relapsed or refractory haematological malignancies is under way; on 3 August 2026, the Company appointed Faiçal Miyara as Chief Business Officer and Jim Ziegler as Chief Commercial Officer.
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