Literature DB >> 17323789

Ethnic sensitivity study of fingolimod in white and Asian subjects.

J M Kovarik1, A Slade, B Voss, H Schmidli, G J Riviere, F Picard, Y Sugita, R Kawai, D Mee-Lee, R L Schmouder.   

Abstract

OBJECTIVE: The authors compared the pharmacokinetics and pharmacological effects of the immunomodulator fingolimod in healthy white and Asian subjects for potential ethnic differences.
METHODS: White and Asian (Japanese) healthy subjects were demographically matched for sex, age and weight. Subjects received single 1.25 mg doses of fingolimod (6 ethnic pairs), 2.5 mg (7 pairs), 5 mg (6 pairs) or 5 mg/day for 7 days (6 pairs). The pharmacokinetics of fingolimod, major metabolites, peripheral blood lymphocyte counts and heart rate were characterized over 1 month after single-dose and 2 months after multiple-dose administration.
RESULTS: There were no clinically relevant differences in the fingolimod dose Cmax or dose AUC relationships between Asian subjects (slopes 0.84 and 1.05) versus white subjects (slopes 1.13 and 1.26) after single-dose administration. During multiple-dose administration, there were no clinically relevant interethnic differences in fingolimod accumulation ratios (6.6 +/- 0.4 for whites, 7.0 +/- 0.7 for Asians), area under the concentration-time curve (390 +/- 73 versus 382 +/- 106 ng x h/ml), or elimination half-life (7.4 +/- 0.8 versus 7.9 +/- 2.0 days). The acute decrease in lymphocyte counts after single- and multiple-dose fingolimod were similar in the two ethnic groups. The lymphocyte recovery rate to baseline after a 5 mg single dose and 5 mg/day multiple dose was reduced by 36 and 15% in Asian subjects compared with white subjects. The transient, acute decrease in heart rate after the first dose of fingolimod and the subsequent return to baseline was similar in the two ethnic groups.
CONCLUSION: There were no marked differences between healthy white and Asian subjects in fingolimod single-dose and multiple-dose pharmacokinetics, lymphocyte trafficking and heart rate responses.

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Year:  2007        PMID: 17323789     DOI: 10.5414/cpp45098

Source DB:  PubMed          Journal:  Int J Clin Pharmacol Ther        ISSN: 0946-1965            Impact factor:   1.366


  7 in total

Review 1.  Clinical pharmacokinetics of fingolimod.

Authors:  Olivier J David; John M Kovarik; Robert L Schmouder
Journal:  Clin Pharmacokinet       Date:  2012-01-01       Impact factor: 6.447

Review 2.  Fingolimod: a review of its use in relapsing-remitting multiple sclerosis.

Authors:  Mark Sanford
Journal:  Drugs       Date:  2014-08       Impact factor: 9.546

Review 3.  Therapeutic potential of targeting sphingosine kinase 1 in prostate cancer.

Authors:  Dmitri Pchejetski; Torsten Böhler; Justin Stebbing; Jonathan Waxman
Journal:  Nat Rev Urol       Date:  2011-09-13       Impact factor: 14.432

4.  FTY720 (fingolimod) increases vascular tone and blood pressure in spontaneously hypertensive rats via inhibition of sphingosine kinase.

Authors:  Léon J A Spijkers; Astrid E Alewijnse; Stephan L M Peters
Journal:  Br J Pharmacol       Date:  2012-06       Impact factor: 8.739

5.  Dose-dependent reduction of lymphocyte count and heart rate after multiple administration of LC51-0255, a novel sphingosine-1-phosphate receptor 1 modulator, in healthy subjects.

Authors:  Inyoung Hwang; Sang Won Lee; Jaeseong Oh; SeungHwan Lee; In-Jin Jang; Kyung-Sang Yu
Journal:  Front Pharmacol       Date:  2022-08-22       Impact factor: 5.988

6.  Pharmacokinetic Interaction Between Fingolimod and Carbamazepine in Healthy Subjects.

Authors:  Olivier J David; Rhett Behrje; Parasar Pal; Hisanori Hara; Christian D Lates; Robert Schmouder
Journal:  Clin Pharmacol Drug Dev       Date:  2018-04-25

7.  Pharmacokinetics and Pharmacodynamics of Cenerimod, A Selective S1P1 R Modulator, Are Not Affected by Ethnicity in Healthy Asian and White Subjects.

Authors:  Pierre-Eric Juif; Jasper Dingemanse; Peter Winkle; Mike Ufer
Journal:  Clin Transl Sci       Date:  2020-09-10       Impact factor: 4.689

  7 in total

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