康柏西普眼用注射液 | China Drugs ListConbercept ophthalmic injection | China Drugs List
本页为公开参考信息，不构成医疗建议、处方或药品供应要约。请向持证专业人士确认当前批准情况、可获得性及适用性。
- 企业
- 成都康弘生物Chengdu Kanghong Biotechnology
- 药品类型
- 生物药Biologic
- 治疗领域
- 眼科Ophthalmology
- 公开来源记录的适应症
- 本品适用于治疗: 1) 新生血管性(湿性)年龄相关性黄斑变性(nAMD); 2) 继发于病理性近视的脉络膜新生血管 (pmCNV)引起的视力损伤; 3) 继发于糖尿病黄斑水肿(DME)引起的视力损伤; 4) 继发于视网膜静脉阻塞(RVO) (视网膜分支静脉阻塞(BRVO)或视网膜中央静脉阻塞(CRVO))的黄斑水肿引起的视力损伤。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).
- 适应症来源与口径
- 来源日期： 2025. 适应症转录自国家医保局公开的企业申报资料；不代表已核实完整的现行说明书。 新增适应症可能由较新的公告或申报资料支持，而非旧版完整说明书；请查看适应症来源。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.
- 说明书信息局限
- 适应症已与官方公开申报资料核对。尚未取得完整原始说明书。Indications checked against an official public submission. The full original prescribing information is still unavailable.
- 中国可获得性状态
- 已核实中国历史批准记录；尚未逐项核查每个产品目前是否持续上市销售。Historical Chinese approval verified; current continuous market availability has not been checked for every product.
- 海外状态
- 待逐一核查各市场。Market-by-market verification pending.
- 医保分类
- 已纳入国家医保（乙类）Included in national insurance (Category B)
- 医保版本
- 2025版；2026年1月1日起执行2025 edition; effective 1 January 2026
- 医保限制
- 限:1.50岁以上的湿性年龄相关性黄斑变性(AMD)；2.糖尿病性黄斑水肿(DME)引起的视力损害；3.脉络膜新生血管(CNV)导致的视力损害；4.继发于视网膜静脉阻塞(RVO)(视网膜分支静脉阻塞(BRVO)或视网膜中央静脉阻塞(CRVO)的黄斑水肿引起的视力损伤。应同时符合以下条件：1.需三级医院眼科或二级及以上眼科专科医院医师处方；2.首次处方时病眼基线矫正视力0.05-0.5；3.事前审查后方可用，初次申请需有血管造影或OCT(全身情况不允许的患者可以提供OCT血管成像)证据；4.每眼累计最多支付9支，第1年度最多支付5支。阿柏西普、雷珠单抗、康柏西普、法瑞西单抗、布西珠单抗的药品支数合并计算。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.
- 医保核查说明
- 按成分／剂型名称精确或标准化匹配。报销仍取决于剂型及目录所列支付限制。Matched by exact or normalized ingredient/formulation name. Reimbursement still depends on the dosage form and listed payment restrictions.