Drug intelligence / Profile preview

opicapone + repaglinide

Development stage
Unknown
Lead developer
Bial
Modality
Small Molecules
Administration
Oral
01

Overview

**Opicapone + repaglinide** is a *combination* of two small molecule pharmaceuticals, not marketed together as a fixed-dose combination but sometimes co-administered. Opicapone is a *peripheral, selective, and reversible catechol-O-methyltransferase (COMT) inhibitor*, used as an adjunct to levodopa preparations in Parkinson’s disease to increase levodopa availability by blocking its peripheral degradation[1][4]. Repaglinide is a *short-acting insulin secretagogue* from the meglitinide class, used to control blood glucose in type 2 diabetes by stimulating rapid, glucose-dependent insulin release from pancreatic beta cells[8]. While opicapone may weakly inhibit the CYP2C8 enzyme that metabolizes repaglinide, clinical studies have found no significant pharmacokinetic interaction when both drugs are co-administered[2][5]. No fixed combination product containing both agents exists, and concomitant use is not a recognized or recommended therapy.

02

Targets

PP2A (Protein phosphatase 2A)COMT (Catechol-O-methyltransferase)ZAP70 (Zeta-chain-associated protein kinase 70)KATP channel (ATP-sensitive potassium channel)TSPO (Translocator Protein (18 kDa))

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