Diroximel fumarate

Diroximel fumarate
Clinical data
Trade namesVumerity
Other namesALKS-8700
AHFS/Drugs.comMonograph
MedlinePlusa620002
License data
Pregnancy
category
  • AU: B3
Routes of
administration
By mouth
ATC code
Legal status
Legal status
  • AU: S4 (Prescription only)
  • US: ℞-only
  • EU: Rx-only
Pharmacokinetic data
Protein bindingMonomethyl fumarate (MMF): 27–45%
MetabolismEsterases, citric acid cycle
MetabolitesMMF (active), hydroxyethyl succinimide (HES, inactive), CO2 (inactive)
Elimination half-life1 hour
ExcretionMMF: 60% lung, 15.5% urine (?), 0.9% faeces
HES: 58–63% urine
Identifiers
  • methyl 2-(2,5-dioxopyrrolidin-1-yl)ethyl (2E)-but-2-enedioate
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC11H13NO6
Molar mass255.226 g·mol−1
3D model (JSmol)
  • COC(=O)C=CC(=O)OCCN1C(=O)CCC1=O
  • InChI=1S/C11H13NO6/c1-17-10(15)4-5-11(16)18-7-6-12-8(13)2-3-9(12)14/h4-5H,2-3,6-7H2,1H3/b5-4+
  • Key:YIMYDTCOUQIDMT-SNAWJCMRSA-N

Diroximel fumarate, sold under the brand name Vumerity, is a medication used for the treatment of relapsing forms of multiple sclerosis (MS). It acts as an immunosuppressant and anti-inflammatory drug. Its most common adverse effects are flushing and gastrointestinal problems.

Diroximel fumarate was approved for medical use in the United States in October 2019, and in the European Union in November 2021.