Conbercept ophthalmic injection | China Drugs List
Public reference information, not medical advice, a prescription or an offer to supply a medicine. Confirm current approval, availability and suitability with licensed professionals.
- Company
- Chengdu Kanghong Biotechnology
- Medicine type
- Biologic
- Therapeutic area
- Ophthalmology
- Indications recorded in the public source
- For treatment of: (1) neovascular (wet) age-related macular degeneration (nAMD); (2) visual impairment due to choroidal neovascularization secondary to pathologic myopia (pmCNV); (3) visual impairment due to diabetic macular edema (DME); and (4) visual impairment due to macular edema secondary to retinal vein occlusion (RVO), including branch retinal vein occlusion (BRVO) or central retinal vein occlusion (CRVO).
- Indication source and scope
- Source date(s): 2025. Indications transcribed from the public NHSA manufacturer submission; this is not verification of the complete current label. Additional indications may be supported by newer announcements or submissions rather than the older full label; see the indication sources.
- Prescribing-information limitations
- Indications checked against an official public submission. The full original prescribing information is still unavailable.
- China availability status
- Historical Chinese approval verified; current continuous market availability has not been checked for every product.
- Overseas status
- Market-by-market verification pending.
- Insurance classification
- Included in national insurance (Category B)
- Insurance edition
- 2025 edition; effective 1 January 2026
- Insurance restrictions
- Restricted to: (1) wet age-related macular degeneration (AMD) in patients over 50 years of age; (2) visual impairment due to diabetic macular edema (DME); (3) visual impairment due to choroidal neovascularization (CNV); or (4) visual impairment due to macular edema secondary to retinal vein occlusion (RVO), including BRVO or CRVO. All of the following must also be met: prescription by an ophthalmologist at a tertiary hospital or a secondary-or-higher specialist eye hospital; baseline corrected visual acuity in the affected eye of 0.05-0.5 at the first prescription; prior authorization, with angiography or OCT evidence for the initial application (OCT angiography may be provided if the patient's systemic condition prevents angiography); and a cumulative maximum of 9 units per eye, including no more than 5 units in the first year. Units of aflibercept, ranibizumab, conbercept, faricimab and brolucizumab are counted together.
- Insurance verification notes
- Matched by exact or normalized ingredient/formulation name. Reimbursement still depends on the dosage form and listed payment restrictions.
Sources
- https://www.cncbd.org.cn/News/Detail/995
- https://www.nhsa.gov.cn/module/download/downfile.jsp?classid=0&filename=a32f9f2f3fc046afaf08471f87456ce3.pdf
- https://www.nhsa.gov.cn/attach/Ypsn2025/YPSN202500175/YPSN202500175.pdf
Open the interactive record, public price references and discussions