盐酸吉卡昔替尼片 | China Drugs ListGecacitinib hydrochloride tablets | 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
苏州泽璟生物制药股份有限公司Suzhou Zelgen Biopharmaceuticals Co., Ltd.
药品类型
化学药Chemical medicine
治疗领域
肿瘤科Oncology
公开来源记录的适应症
(1)用于中危或高危原发性骨髓纤维化(PMF)、真性红细胞增多症继发性骨髓纤维化(PPV-MF)和原发性血小板增多症继发性骨髓纤维化(PET-MF)的成人患者,治疗疾病相关脾肿大或症状;(2)成人重度斑秃。1. Adults with intermediate- or high-risk primary myelofibrosis (PMF), post-polycythemia vera myelofibrosis (PPV-MF), or post-essential thrombocythemia myelofibrosis (PET-MF), for treatment of disease-related splenomegaly or symptoms. 2. Severe alopecia areata in adults.
适应症来源与口径
来源日期: 2025-05, 2026-06-15. 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): 2025-05, 2026-06-15. 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
限中危或高危原发性骨髓纤维化(PMF)、真性红细胞增多症继发性骨髓纤维化(PPV-MF)和原发性血小板增多症继发性骨髓纤维化(PET-MF)的成人患者。Limited to adults with intermediate- or high-risk PMF, PPV-MF, or PET-MF.
医保期限
2026-01-01 至 2027-12-312026-01-01 to 2027-12-31
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.

来源

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