| Clinical data | |
|---|---|
| Trade names | Mepsevii |
| Other names | Vestronidase alfa-vjbk |
| AHFS/Drugs.com | Monograph |
| License data | |
| Routes of administration | Injection |
| ATC code | |
| Legal status | |
| Legal status |
|
| Identifiers | |
| CAS Number | |
| UNII | |
| KEGG | |
| Chemical and physical data | |
| Formula | C3308H4996N874O940S16 |
| Molar mass | 72562.49 g·mol−1 |
Vestronidase alfa, sold under brand name Mepsevii, is a medication for the treatment of Sly syndrome.[4] It is a recombinant form of the human enzyme beta-glucuronidase. It was approved in the United States in November 2017, to treat children and adults with an inherited metabolic condition called mucopolysaccharidosis type VII (MPS VII), also known as Sly syndrome.[5][6] MPS VII is an extremely rare, progressive condition that affects most tissues and organs.[5]
The most common side effects after treatment with vestronidase alfa include infusion site reactions, diarrhea, rash (urticaria) and anaphylaxis (sudden, severe allergic reaction).[5][2]
The US. Food and Drug Administration (FDA) considers it to be a first-in-class medication.[7] It was approved for use in the European Union in August 2018.[2]
Mepsevii is indicated for the treatment of non-neurological manifestations of Mucopolysaccharidosis VII (MPS VII; Sly syndrome).[2][8]
The safety and efficacy of vestronidase alfa were established in a clinical trial and expanded access protocols enrolling a total of 23 participants ranging from five months to 25 years of age.[5] Participants received treatment with vestronidase alfa at doses up to 4 mg/kg once every two weeks for up to 164 weeks.[5] Efficacy was primarily assessed via the six-minute walk test in ten participants who could perform the test.[5] After 24 weeks of treatment, the mean difference in distance walked relative to placebo was 18 meters.[5] Additional follow-up for up to 120 weeks suggested continued improvement in three participants and stabilization in the others.[5] Two participants in the vestronidase alfa development program experienced marked improvement in pulmonary function.[5] Overall, the results observed would not have been anticipated in the absence of treatment.[5] The effect of vestronidase alfa on the central nervous system manifestations of MPS VII has not been determined.[5]
The FDA approved vestronidase alfa-vjbk based primarily on evidence from one clinical trial (NCT02230566) of 12 participants with mucopolysaccharidosis VII. The trial was conducted at four sites in the United States.[6]
The benefit and side effects of vestronidase alfa were based primarily on one trial.[6] Participants were randomly assigned to four groups.[6] Three groups of participants received placebo treatment before starting vestronidase alfa treatment and one group received vestronidase alfa only.[6] vestronidase alfa or placebo were given once every two weeks as intravenous (IV) infusions.[6] Neither participants nor healthcare providers knew which treatment was given until after the trial was competed.[6]
The benefit of 24 weeks of vestronidase alfa treatment was primarily evaluated by the 6-minute walking test (6MWT) and compared to placebo treatment in ten participants who could perform the test.[6] The 6MWT measured the distance a patient could walk on a flat surface in 6 minutes.[6] An additional follow-up using 6MWT was done for up to 120 weeks.[6]
The application for vestronidase alfa was granted fast track designation, orphan drug designation, and a rare pediatric disease priority review voucher.[5] This was the twelfth rare pediatric disease priority review voucher issued.[5]
The US Food and Drug Administration (FDA) granted approval of Mepsevii to Ultragenyx Pharmaceutical, Inc,[5] and required the manufacturer to conduct a post-marketing study to evaluate the long-term safety of the product.[5]
This article incorporates text from this source, which is in the public domain.
This article incorporates text from this source, which is in the public domain.
