Zhaoke Ophthalmology (6622) H1 2026 earnings summary
Event summary combining transcript, slides, and related documents.
H1 2026 earnings summary
6 Oct, 2026Executive summary
H1 revenue increased to RMB18.8m from RMB15.8m YoY; reported loss widened to RMB122.6m from RMB116.6m, while adjusted loss was RMB116.1m versus RMB115.3m.
Cyclosporine Ophthalmic Gel, Atropine Sulfate Eye Drops and bevacizumab intravitreal injection (TAB014) remained under China regulatory review; launch preparations continued.
Cash, cash equivalents and time deposits over three months totaled RMB715.8m at June 30, 2026, excluding pledged balances.
Financial highlights
Revenue was RMB18.8m versus RMB15.8m YoY; gross profit was RMB9.7m versus RMB8.5m, and drug and product sales were RMB17.6m versus RMB15.1m.
Net loss was RMB122.6m versus RMB116.6m; adjusted loss excluding equity-settled share-based payment expenses was RMB116.1m versus RMB115.3m.
Other income fell to RMB14.7m from RMB26.3m, mainly due to lower bank interest income; other net gain rose to RMB21.7m from RMB20.0m, mainly from FX gains.
R&D expense decreased to RMB105.8m from RMB113.1m; G&A rose to RMB33.2m from RMB30.6m, and selling and distribution expense to RMB24.8m from RMB23.4m.
Operating cash use was RMB88.8m versus RMB149.0m; period-end cash and equivalents were RMB497.6m versus RMB959.3m at 2025 year-end.
Outlook and guidance
Potential China approvals for the three lead drugs remained targeted during 2026; launch preparations include nationwide distribution, hospital coverage, digital channels and in-house manufacturing.
Target is 12 commercialized drugs by end-2026, supported by nationwide sales, digital channels and in-house manufacturing.
Overseas revenue is expected to begin in H2 2027, subject to marketing authorizations and commercialization progress; partnered YUVEZZI markets are also expected to contribute from H2 2027, subject to approvals.
Cyclosporine gel’s GCC application remained under review, Australian generic registrations were at an advanced stage, and the first CDMO product application was planned for U.S. FDA submission in 2026.
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