Effect of Opicapone Tablets on Levodopa and 3-O-Methyldopa Pharmacokinetics in Healthy Japanese Subjects : Phase 1 Study

© 2020 The Authors. Clinical Pharmacology in Drug Development published by Wiley Periodicals LLC on behalf of American College of Clinical Pharmacology..

This study evaluated the effect of a small-tablet formulation of opicapone for use in clinical trials in Japan on the pharmacokinetics of levodopa (l-dopa) and 3-O-methyldopa (3-OMD). In an open-label, 3-period, single-sequence crossover phase 1 study in 80 healthy Japanese males (aged 20-45 years; body mass index, 18.5 to <30.0 kg/m2 ), 10 mg of l-dopa/carbidopa 100 was administered 3 times daily on day 0 (period 1) and day 12 (period 3), and opicapone tablets (5, 10, 25, or 50 mg; n = 20 each group) were administered once daily for 11 days (period 2). During periods 1 and 3, plasma concentrations of l-dopa and 3-OMD were measured and pharmacokinetic parameters (maximum observed plasma concentration, time at which maximum concentration was observed, area under the plasma concentration-time curve from time 0 to 5 hours [AUC5h ] and from time 0 to 24 hours [AUC24h ] following each dose, terminal half-life) of plasma l-dopa and 3-OMD were determined along with the geometric mean ratio (period 3/period 1) of AUC24h for l-dopa and 3-OMD. Maximum concentration of l-dopa for the first, second, or third doses of l-dopa/carbidopa did not significantly increase with increasing opicapone dose. The AUC of l-dopa increased with increasing opicapone dose but tended toward a peak plateau with opicapone doses of 25 mg and higher. Geometric mean ratios (90% confidence intervals) of AUC24h were 5 mg, 1.16 (1.10-1.21); 10 mg, 1.26 (1.23-1.30); 25 mg, 1.51 (1.44-1.57); 50 mg, 1.60 (1.54-1.66). Opicapone tablets were well tolerated. In Japanese healthy subjects, increases in plasma exposure to l-dopa appear to level off with opicapone doses of 25 mg and higher, which may be relevant for optimal dosing among Japanese patients with Parkinson disease.

Medienart:

E-Artikel

Erscheinungsjahr:

2021

Erschienen:

2021

Enthalten in:

Zur Gesamtaufnahme - volume:10

Enthalten in:

Clinical pharmacology in drug development - 10(2021), 2 vom: 24. Feb., Seite 180-189

Sprache:

Englisch

Beteiligte Personen:

Nomoto, Masahiro [VerfasserIn]
Takeda, Atsushi [VerfasserIn]
Iwai, Katsuaki [VerfasserIn]
Nishimura, Akihisa [VerfasserIn]
Hattori, Nobutaka [VerfasserIn]

Links:

Volltext

Themen:

3-OMD
3-methoxytyrosine
42HK56048U
46627O600J
Antiparkinson Agents
COMT inhibitor
Carbidopa
Carbidopa, levodopa drug combination
Catechol O-Methyltransferase Inhibitors
Clinical Trial, Phase I
Drug Combinations
Japanese
Journal Article
Levodopa
MNX7R8C5VO
Opicapone
Oxadiazoles
Parkinson disease
Pharmacokinetic
Phase 1
Research Support, Non-U.S. Gov't
Tablets
Tyrosine
V3O7J20DWN
Y5929UIJ5N

Anmerkungen:

Date Completed 14.12.2021

Date Revised 07.12.2022

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1002/cpdd.799

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM309987059