沃索里肽,一种神奇的药物,覆盖了软骨发育不全的未满足需求:监管更新。

IF 1.1 Q2 MEDICINE, GENERAL & INTERNAL Intractable & rare diseases research Pub Date : 2023-11-01 DOI:10.5582/irdr.2023.01055
Simran, Kirthiga Devi S S, Sabanis Chetan Dushantrao, Ramesh Joga, Sandeep Kumar
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引用次数: 0

摘要

侏儒症是一种罕见的以身材矮小为特征的疾病。软骨发育不全被认为是侏儒症的主要原因。虽然这种情况不会危及生命,但它会极大地影响患者的社交生活。美国食品和药物管理局(FDA)首次批准了治疗软骨发育不全的药物Voxzogo (vosoritide)。该药还通过集中程序获得了欧洲药品管理局(EMA)的批准。该药与血压降低有关,这是一种严重的不良反应。然而,这种不良事件/风险已被利益所克服,即满足了未满足的医疗需求。在美国,该药获得了加速批准,因为它符合罕见儿科疾病的标准。这篇综述包括详细的孤儿药批准过程,特别是关于vosoritide,它被认为是软骨发育不全治疗的一个里程碑。
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Vosoritide, a miracle drug, covering unmet need in achondroplasia: A regulatory update.

Dwarfism is a rare condition characterized by small stature. Achondroplasia is predominantly considered the leading cause of dwarfism. Although the condition is not life-threatening, it dramatically impacts the social life of the patient. The United States Food and Drug Administration (US FDA) first approved the drug Voxzogo (vosoritide) for achondroplasia. The drug also received approval from the European Medicines Agency (EMA) via the centralized procedure. The drug is associated with a decrease in blood pressure, a severe adverse event. However, this adverse event/risk has been overcome by benefits, i.e. fulfilling of unmet medical need. In the United States, the drug received accelerated approval as it satisfied the criteria of rare pediatric disease. This review includes a detailed orphan drug approval process with particular reference to vosoritide, which is considered a milestone for the treatment of achondroplasia.

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来源期刊
Intractable & rare diseases research
Intractable & rare diseases research MEDICINE, GENERAL & INTERNAL-
CiteScore
2.10
自引率
0.00%
发文量
29
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