别名 DISORDERS OF THE UREA CYCLE METABOLISM、Disorder of the urea cycle metabolism、Disorder of the urea cycle metabolism (disorder) + [28] |
简介 Rare congenital metabolism disorders of the urea cycle. The disorders are due to mutations that result in complete (neonatal onset) or partial (childhood or adult onset) inactivity of an enzyme, involved in the urea cycle. Neonatal onset results in clinical features that include irritability, vomiting, lethargy, seizures, NEONATAL HYPOTONIA; RESPIRATORY ALKALOSIS; HYPERAMMONEMIA; coma, and death. Survivors of the neonatal onset and childhood/adult onset disorders share common risks for ENCEPHALOPATHIES, METABOLIC, INBORN; and RESPIRATORY ALKALOSIS due to HYPERAMMONEMIA. |
靶点 |
作用机制 精氨酸酶替代物 |
在研适应症 |
最高研发阶段批准上市 |
首次获批国家/地区 欧盟 [+3] |
首次获批日期2023-12-15 |
靶点- |
作用机制 脂肪酸替代品 [+1] |
最高研发阶段批准上市 |
首次获批国家/地区 美国 |
首次获批日期2020-06-30 |
靶点- |
作用机制 氨清除剂 |
最高研发阶段批准上市 |
首次获批国家/地区 美国 |
首次获批日期2013-02-01 |
开始日期2024-11-15 |
申办/合作机构 |
开始日期2024-09-27 |
申办/合作机构 锐康迪(北京)医药有限公司 [+2] |
开始日期2024-08-30 |
申办/合作机构 |