- Zhaoke Ophthalmology reported regulatory milestones that could expand its near-term commercial portfolio, led by three flagship assets positioned for large ophthalmology markets in China and internationally.
- In China, 国家药监局 accepted the biological products license application for 贝伐单抗玻璃体腔内注射液 (TAB014), supporting a potential first-mover position in a wAMD-focused bevacizumab filing.
- For 硫酸阿托品滴眼液 (NVK002), 国家药监局 accepted the simplified new drug application for the 0.01% dose and accepted the new drug application for the 0.02% dose, keeping both formulations under review as potential growth drivers.
- In the US, FDA approved the new drug investigational application for 环孢素眼用凝胶 to start a Phase III trial, which could strengthen partnering options and broaden the addressable market beyond Greater China.
- Commercial readiness was supported by RMB 959 million in cash and cash equivalents, while loss narrowed to RMB 209 million.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Zhaoke Ophthalmology Ltd. published the original content used to generate this news brief via IIS, the Issuer Information Service operated by the Hong Kong Stock Exchange (HKex) (Ref. ID: HKEX-EPS-20260325-12067098), on March 25, 2026, and is solely responsible for the information contained therein.