Drug intelligence / Profile preview

vyalev

Development stage
Approved
Lead developer
AbbVie
Modality
Metabolically Activated Prodrugs → Prodrugs/Conditional Activator Small Molecules → Small Molecules
Administration
Subcutaneous
01

Overview

Vyalev is a fixed-dose combination drug containing the prodrugs foscarbidopa and foslevodopa. It is indicated for the treatment of motor fluctuations in adults with advanced Parkinson’s disease. Both components are administered as a continuous 24-hour subcutaneous infusion using a wearable pump (Vyafuser). Foscarbidopa is converted in vivo to carbidopa, an aromatic amino acid decarboxylase inhibitor that prevents peripheral breakdown of levodopa. Foslevodopa is converted to levodopa, which crosses the blood-brain barrier and is then metabolized to dopamine in the brain. This dual mechanism increases central dopamine levels while minimizing peripheral side effects by reducing systemic conversion of levodopa to dopamine before it reaches the brain. Vyalev was developed as an alternative to oral or intestinal gel formulations of carbidopa/levodopa, offering more stable plasma concentrations and improved control over motor symptoms for patients with advanced disease[1][2][3][4][8][10].

Brand names
VyalexProduodopa
Other names
foscarbidopa and foslevodopafoscarbidopa/foslevodopa
02

Targets

DRD (Dopamine receptors)DDC (Aromatic L-amino acid decarboxylase)

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