Pharmacokinetics and safety of single and multiple doses of rasagiline in healthy Japanese and caucasian subjects
| Autor: | Eli Eyal, Aviva Gross, Ofer Spiegelstein, Laura Rabinovich-Guilatt, Anna Elgart |
|---|---|
| Rok vydání: | 2018 |
| Předmět: |
Single administration
Adult Male medicine.medical_specialty Cmax Toxicology Placebo Multiple dosing 030226 pharmacology & pharmacy Gastroenterology Drug Administration Schedule White People Antiparkinson Agents 03 medical and health sciences chemistry.chemical_compound Young Adult 0302 clinical medicine Pharmacokinetics Asian People Double-Blind Method Internal medicine medicine Humans Pharmacology Rasagiline business.industry Healthy subjects General Medicine chemistry Pharmacodynamics Indans Female business 030217 neurology & neurosurgery |
| Zdroj: | Basicclinical pharmacologytoxicology. 124(3) |
| ISSN: | 1742-7843 |
| Popis: | As of March 2018, rasagiline is approved for the treatment of Parkinson disease in 55 countries including Japan. The present study evaluated the pharmacokinetics (PK) and safety of rasagiline in healthy Japanese and Caucasian subjects following single and multiple administrations of three rasagiline doses. In this double-blind, placebo-controlled study, 64 healthy subjects (32 Japanese and 32 Caucasian) received either rasagiline (0.5, 1.0, or 2.0 mg) or placebo for 10 days with PK sampling for single-dose administration on day 1 and for multiple administration on day 10. Regardless of administration schedule, rasagiline plasma concentrations and dose-related increases in exposure parameters were similar between Japanese and Caucasians. Rasagiline accumulation (2-fold for 0.5 mg and 3-fold for 1.0 mg and 2.0 mg doses) following multiple administration was similar across the ethnic groups. Geometric mean ratios (GMR) comparing Japanese to Caucasians for AUC0-24 , Cmax and AUCinf following single administration were 1.38, 1.17 and 1.38 for 0.5 mg; 1.22, 1.20 and 1.22 at 1.0 mg; and 1.02, 1.00 and 1.02 at for 2.0 mg. GMR for AUCtau and Cmax,ss following multiple administration were 1.43 and 1.06 at 0.5 mg, 1.06 and 1.00 at 1.0 mg, and 1.09 and 1.07 at 2.0 mg. Safety measures were unremarkable and similar between Caucasian and Japanese subjects. Comparable systemic exposure and safety parameters were demonstrated for rasagiline administered to healthy Japanese and Caucasian subjects. |
| Databáze: | OpenAIRE |
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