Miglustat
| Clinical data | |
|---|---|
| Trade names | Zavesca, Brazaves, Opfolda |
| Other names | OGT 918, 1,5-(butylimino)-1,5-dideoxy-D-glucitol, N-butyl-deoxynojirimycin (NB-DNJ) |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a604015 |
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| Routes of administration | By mouth |
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| Legal status | |
| Pharmacokinetic data | |
| Bioavailability | 97% |
| Protein binding | Nil |
| Metabolism | Nil |
| Elimination half-life | 6–7 hours |
| Excretion | Kidney, unchanged |
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| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.216.074 |
| Chemical and physical data | |
| Formula | C10H21NO4 |
| Molar mass | 219.281 g·mol−1 |
| 3D model (JSmol) | |
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Miglustat, sold under the brand name Zavesca among others, is a medication used to treat type I Gaucher disease[7] and Pompe disease.[10]
It was approved for medical use in the European Union in November 2002,[7][11] and for medical use in the United States in July 2003.[12][13]
- ^ "Miglustat (Zavesca) Use During Pregnancy". Drugs.com. 4 February 2020. Archived from the original on 28 November 2020. Retrieved 7 August 2020.
- ^ "Summary for ARTG Entry:122957 Zavesca miglustat 100 mg capsules blister pack". Therapeutic Goods Administration.
- ^ "Zavesca (miglustat) 100 mg hard capsules - Summary of Product Characteristics (SmPC)". (emc). Archived from the original on 25 February 2021. Retrieved 7 August 2020.
- ^ "Zavesca- miglustat capsule". DailyMed. 20 April 2023. Retrieved 2 October 2023.
- ^ "Yargesa- miglustat capsule". DailyMed. 12 July 2023. Retrieved 2 October 2023.
- ^ "Opfolda (miglustat) capsules prescribing information" (PDF). Food and Drug Administration. September 2023.
- ^ a b c "Zavesca EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 5 August 2020. Retrieved 7 August 2020.
- ^ "Opfolda EPAR". European Medicines Agency (EMA). 7 July 2023. Retrieved 7 July 2023.
- ^ "Yargesa EPAR". European Medicines Agency. 11 April 2023. Retrieved 2 October 2023.
- ^ Cite error: The named reference
Opfolda: Pending EC decisionwas invoked but never defined (see the help page). - ^ European Medicines Agency. Human Medicines Database. Zavesca (miglustat) Archived 7 January 2016 at the Wayback Machine Page Accessed 1 September 2014.
- ^ "Drug Approval Package: Zavesca (Miglustat) NDA #021348". U.S. Food and Drug Administration (FDA). 4 April 2002. Archived from the original on 27 February 2021. Retrieved 9 August 2020.
- ^ Actelion Press Release August 2003. Zavesca approved -- first oral treatment option for type 1 Gaucher disease Archived 3 March 2016 at the Wayback Machine