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Givosiran

Generic Name
Givosiran
Brand Names
Givlaari
Drug Type
Biotech
CAS Number
1639325-43-1
Unique Ingredient Identifier
ROV204583W

Overview

Givosiran is a small interfering RNA (siRNA) directed towards 5-aminolevulinic acid synthase, a critical enzyme in the heme biosynthesis pathway. It is manufactured by Alnylam Pharmaceuticals and was first approved for use in the United States in November 2019 for the treatment of adults with acute hepatic porphyria, a genetic disorder in which the overproduction of toxic heme intermediates leads to neuro-, nephro-, and gastrotoxicity. Givosiran represents an important step forward in the treatment of acute hepatic porphyria as it is the first approved pharmacotherapy for the prevention of acute attacks - previous strategies involved non-therapeutic measures (e.g. trigger avoidance), intravenous hemin for the treatment of attacks, and liver transplantation in refractory cases. Givosiran is the second-ever FDA-approved member of the siRNA drug class (the first being patisiran), a new class of drugs promising an important and exciting step forward in the treatment of genetic disorders.

Background

Givosiran is a small interfering RNA (siRNA) directed towards 5-aminolevulinic acid synthase, a critical enzyme in the heme biosynthesis pathway. It is manufactured by Alnylam Pharmaceuticals and was first approved for use in the United States in November 2019 for the treatment of adults with acute hepatic porphyria, a genetic disorder in which the overproduction of toxic heme intermediates leads to neuro-, nephro-, and gastrotoxicity. Givosiran represents an important step forward in the treatment of acute hepatic porphyria as it is the first approved pharmacotherapy for the prevention of acute attacks - previous strategies involved non-therapeutic measures (e.g. trigger avoidance), intravenous hemin for the treatment of attacks, and liver transplantation in refractory cases. Givosiran is the second-ever FDA-approved member of the siRNA drug class (the first being patisiran), a new class of drugs promising an important and exciting step forward in the treatment of genetic disorders.

Indication

用于治疗急性肝卟啉症(AHP)。 AHP是一类非常罕见的遗传性疾病(罕见病),其特征是使人衰弱的、潜在危及生命的发作,对一些患者来说,疾病的慢性表现会对日常功能和生活质量产生负面影响。AHP的长期并发症包括慢性神经性疼痛、高血压、慢性肾病和肝病。

Associated Conditions

  • Acute Hepatic Porphyria (AHP)

FDA Approved Products

No FDA products found for this drug

Singapore Approved Products

No Singapore products found for this drug

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