遗传性血管性水肿
Hereditary angioedema
定义 英文原文(暂无中文)
Hereditary angioedema (HAE) is a genetic disease characterized by the occurrence of transitory and recurrent subcutaneous and/or submucosal edemas resulting in swelling and/or abdominal pain.
别名
遗传性肺组胺介导血管性水肿
基本事实
- 遗传方式
- 常染色体显性
- 发病年龄
- 各年龄段
- 患病率
- 1-9 / 100 000(Europe)
相关基因 7来自下位疾病
Orphanet 未在本条目上直接标注致病基因。下表由本组所属的下位疾病汇总而来,「来源条目」列给出基因实际标注在哪一个 ORPHA 条目上。
| 基因 | 名称 | 来源条目 |
|---|---|---|
| ANGPT1 | angiopoietin 1 | ORPHA:599418 |
| F12 | coagulation factor XII | ORPHA:100054 |
| HS3ST6 | heparan sulfate-glucosamine 3-sulfotransferase 6 | ORPHA:599418 |
| KNG1 | kininogen 1 | ORPHA:599418 |
| MYOF | myoferlin | ORPHA:599418 |
| PLG | plasminogen | ORPHA:537072 |
| SERPING1 | serpin family G member 1 | ORPHA:100050 |
近两年的全球研究 969L2
2024/08 起在 Europe PMC 检索所得,按发表时间倒序显示最近 20 篇。标题未译成中文——自动翻译需要接入 LLM 服务,尚未引入。
- 2026-08Would the number of new cases of hereditary angioedema decrease due to declining fertility rates?
- 2026-08综述[Current and future therapies for bradykinin-mediated angioedema]
- 2026-08Sustained Effectiveness of Lanadelumab in Preventing Hereditary Angioedema Attacks: The ENABLE Study
- 2026-07Berotralstat During Pregnancy in a Patient With Hereditary Angioedema
- 2026-07综述Lonvoguran ziclumeran: a CRISPR-CAS9-based gene therapy for the treatment of hereditary angioedema
- 2026-07综述[What are angioedemas and how are they classified?]
- 2026-07Hereditary Angioedema: On-demand Treatment and Long-term Prophylaxis - A Global Reality
- 2026-07Optimizing conversations on treatment management in hereditary angioedema: healthcare professional and patient perspectives on long-term prophylaxis and shared decision-making
- 2026-07病例报告The peri-operative management of patients with hereditary angioedema requiring dental treatment: a case series
- 2026-07系统综述Prevalence and Incidence of Hereditary Angioedema: A Systematic Literature Review
- 2026-07Clinical expressions, disease course, quality of life, and resilience in subgroups of patients with angioedema
- 2026-07病例报告Living-Donor Kidney Transplantation Between Mother and Son With Clinically Confirmed Hereditary Angioedema
- 2026-07系统综述Icatibant for acute hereditary angioedema attacks in pediatric patients: A systematized review
- 2026-06Beyond scientific advances: delays, disparities, and opportunities in hereditary angioedema care across Latin America
- 2026-06综述Isolated angioedema in the emergency department: rarely an allergic reaction
- 2026-06Improving capability, opportunity and motivation to support hereditary angioedema patients experiencing life threatening attacks: Pilot evaluation of a video-based training tool for healthcare professionals
- 2026-06Clinical experience with berotralstat in patients with hereditary angioedema: an Italian case series from the ITACA cohort
- 2026-06Burden of Hereditary Angioedema in Adults: Impact of Disease and Patient Characteristics
- 2026-06Modeling Hereditary Angioedema With Personalized EPSC-Derived Hepatocytes: A CRISPR-Validated Platform for Mutation-Specific Mechanisms and Therapeutic Innovation
- 2026-06Psychometric validation of the Angioedema Quality of Life Questionnaire (AE-QoL) for hereditary angioedema
国家医保药品目录中点名本病的药品 2L2
出自《国家基本医疗保险、生育保险和工伤保险药品目录(2025年)》(医保发〔2025〕33号,2026-01-01 起执行)。下列药品在药品名称或限定支付范围里出现了本病的名称。
匹配不到 ≠ 不能报销。目录里只有约一成药品设了限定支付范围,其余按适应症正常使用同样可报销;本区块只能回答「目录有没有点名这个病」,不能回答「这个病有没有药能报销」。各省执行细则、双通道与单独支付范围另有规定,请以当地医保部门口径为准。
- 拉那利尤单抗注射液乙类谈判药品限12岁及以上患者预防遗传性血管性水肿(HAE)发作。
- 醋酸艾替班特注射液乙类西药限成人、青少年和≥2 岁儿童的遗传性血管性水肿(HAE)急性发作。
境外已获批用于本病的药物 11L2
欧盟 8 项、美国 3 项。同一药物在两地各批一次的,会分别列出。
「境外已获批」不等于「在中国能用」。中间隔着进口注册、临床急需境外新药通道、海南博鳌乐城国际医疗旅游先行区等几条路径,各有各的条件与费用。这一节能确定地告诉你的只有一件事:这个病在世界范围内已经有获得批准的药物,它叫什么名字。拿这个名字去问主治医生,是下一步最省力的做法。
药名一律保留英文原文,不作翻译——中国的药品通用名与英文名的音译经常不一致,译错会让人去找一个不存在的药。
- Firazyr欧盟2008-07-11icatibant官方记录
- Ruconest欧盟2010-10-28conestat alfa官方记录
- Cinryze欧盟2011-06-15C1 inhibitor (human)官方记录
- Takhzyro欧盟2018-11-22lanadelumab官方记录
- Orladeyo欧盟2021-04-30berotralstat官方记录
- Andembry欧盟2025-02-10garadacimab官方记录
- Ekterly欧盟2025-09-17sebetralstat官方记录
- Dawnzera欧盟2026-01-19donidalorsen官方记录
- Berinert美国2009-10-08C1 esterase inhibitor (human)官方记录
- Haegarda美国2017-06-22C1 esterase inhibitor subcutaneous (human)官方记录
- Dawnzera美国2025-08-21donidalorsen官方记录
已获孤儿药资格、尚未获批的在研药物(7 项)
孤儿药资格只是一种监管身份——它意味着监管机构认可这是罕见病用药并给予研发激励,不代表这个药已被证明有效,也不代表将来一定能上市。绝大多数最终不会成药。列在这里是为了看清有哪些方向正在被尝试。
- R)-1-(3-(aminomethyl) phenyl)-N-(5-((3-cyanophenyl)(cyclopropylmethyla欧盟2018-06-27Treatment of hereditary angioedema官方记录
- messenger RNA encoding Cas9, single guide RNA targeting the human KLKB欧盟2023-11-08Treatment of hereditary angioedema官方记录
- navenibart欧盟2024-11-10Treatment of hereditary angioedema官方记录
- adeno-associated virus serotype 5 (AAV5) vector containing the hSERPIN美国2021-12-20Treatment of hereditary angioedema官方记录
- lipid nanoparticle encapsulating single guide RNA (G012267) targeting 美国2022-09-01Treatment of hereditary angioedema官方记录
- navenibart美国2024-09-26treatment of hereditary angioedema官方记录
- small interfering RNA duplex oligonucleotide designed to cleave prekal美国2025-10-02treatment of hereditary angioedema官方记录
数据来自欧洲药品管理局(EMA)的药品与孤儿药资格公开导出表,以及美国 FDA 孤儿药资格数据库。两边口径不同:欧盟一侧取的是当前状态仍为「已授权」的药品;美国一侧记录的是「曾获批准」这一事实,FDA 的公开表不追踪药物此后是否退市(例如 Relyvrio 于 2024 年撤市,表中仍记为已获批)。请以官方记录页为准。
在中国开展的临床试验 6L2
按病名在 ClinicalTrials.gov 检索、并校验研究中心含中国大陆而来。登记状态不等于现在真的能入组——务必按 NCT 号到原站核实,并与主治医生商量。
登记为可入组 3
- 招募中NCT06679881Long-Term, Open-label Study of Oral Deucrictibant Extended-Release Tablet for Prophylaxis Against Angioedema Attacks in Adolescents and Adults With HAE中国研究中心 1 个:Beijing
- 招募中NCT06960213STOP-HAE: A Phase 3 Study of ADX-324 in HAE中国研究中心 3 个:Beijing、Harbin、Zhengzhou
- 招募中NCT07428499Phase 3 Extension Study of ADX-324 in Participants With Hereditary Angioedema (HAE)中国研究中心 3 个:Beijing、Harbin、Zhengzhou
其他状态的试验(3 项)
- 已完成NCT05460325A Study of Lanadelumab (SHP643) in Chinese Participants With Hereditary Angioedema (HAE)中国研究中心 4 个:Beijing、Guangzhou、Wuhan、Yantai
- 已完成NCT06346899A Study of Lanadelumab (Takhzyro) and Icatibant (Firazyr®) in Persons With HAE in China中国研究中心 13 个:Chengdu、Fuzhou、Guangzhou、Hangzhou、Jinan、Kunming 等 12 地
- 进行中·不再招募NCT06846398A Phase 2 in Adult Subjects With Hereditary Angioedema中国研究中心 6 个:Beijing、Chengdu、Kunming、Lanzhou、Wuhan、Yantai
中国境外的在招试验 27L2
这些试验在中国没有研究中心,通常无法直接报名——入组一般要求在当地居住并接受随访。列在这里是因为它另有用处:看清楚全世界正在试哪些药、做到了哪一期、由谁在做。把药名和 NCT 编号记下来去问主治医生,或据此进一步查该药是否已在境外获批、是否有拓展性用药(expanded access)通道。
CT.gov 报告命中 27 项,此处取回并展示最近的 15 项。
- 尚未开始招募NCT07218393A Study About the Diagnosis and Management of Hereditary Angioedema (HAE) in Egypt埃及
- 尚未开始招募NCT07445087A Study of Takhzyro in Teenagers and Adults With Hereditary Angioedema (HAE) in South Korea
- 尚未开始招募NCT07654829Safety and Effectiveness of Sebetralstat (KVD900) for Short-Term Prophylaxis Before Procedures in People With Hereditary Angioedema (KONTROL)美国
- 招募中NCT07293364A Study to Learn About the C1-Inhibitor Function as Diagnosis for Hereditary AngioedemaAlgeria
- 招募中NCT07263685A Study of Lanadelumab in Teenagers and Adults With Hereditary Angioedema (HAE) in the Kingdom of Saudi Arabia沙特阿拉伯
- 招募中NCT07298447Donidalorsen Treatment in Children With Hereditary Angioedema意大利、波兰、西班牙、美国
- 招募中NCT07448181Real-life Ecological Momentary Assessment of Lived Burden in Hereditary AngioEdema意大利
- 招募中NCT07266805Study of Oral Deucrictibant XR Tablet for Prophylaxis and Deucrictibant IR Capsule for On-Demand Treatment of Angioedema Attacks in Adults With Acquired Angioedema Due to C1 Inhibitor Deficiency澳大利亚、奥地利、保加利亚、加拿大、法国、德国、匈牙利、意大利 等 16 国
- 招募中NCT06919003Improving Deceased-Donor Kidney Transplant Outcomes Via a Single Intragraft Injection of C1 Esterase Inhibitor (IMPROVE TRIAL)美国
- 招募中NCT07021495SKIN Disease Profiling by an Exploratory, pRospective, Biomarker Study in dermatoloGY Practice (SKINERGY)荷兰
- 招募中NCT07001280A Study Investigating the Effectiveness and Safety of Garadacimab for Treating Patients With Hereditary Angioedema (HAE)奥地利、加拿大、德国、英国、美国
- 招募中NCT07046806Oral Deucrictibant for Prophylactic and Acute Treatment in Hereditary Angioedema Patients美国
- 尚未开始招募NCT06811467Suicide Ideation in Hereditary Angioedema
- 招募中NCT06782230ScATtEred Rare Disease Biobanks: a Model of Sample/Data Collection With susTainablE and Shared Criteria意大利
- 招募中NCT06573723Institutional Registry of Rare Diseases阿根廷
外部标识与链接
发现这一页有错误?告诉我 · 邮件主题会自动带上本页的 ORPHA 编号
本页数据来源
- 疾病定义、同义词、基因、表型、流行病学:Orphanet(CC BY 4.0)
- 中文病名:Orphanet 中文包,冻结于 2020-06-01
- 表型中文标签:HPO 简体中文翻译(CHPO 上游成果)