Literature DB >> 28913826

Modeling Tolerance Development for the Effect on Heart Rate of the Selective S1P1 Receptor Modulator Ponesimod.

Dominik Lott1,2, Thorsten Lehr1, Jasper Dingemanse2, Andreas Krause2.   

Abstract

Ponesimod is a selective sphingosine-1-phosphate-1 (S1P1 ) receptor modulator currently under investigation for the treatment of multiple sclerosis. S1P receptor modulators reduce heart rate following treatment initiation. This effect disappears with repeated dosing, enabling development of innovative uptitration regimens to optimize patient safety. There are currently no published pharmacokinetic/pharmacodynamic models describing the heart rate reduction of S1P receptor modulators in humans. The model developed here provides quantification of this effect for ponesimod. A direct-effect Imax model with estimated maximum reduction of 45%, tolerance development, and circadian variation best described this effect. The pooled data from nine clinical studies enabled characterization of interindividual variability. The model was used to simulate different treatment regimens to compare the effect of high initial doses vs. gradual uptitration with respect to the occurrence of bradycardia. The results indicate a better safety profile when using gradual uptitration. The model allows studying dosing regimens not clinically tested in silico.
© 2017 American Society for Clinical Pharmacology and Therapeutics.

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Year:  2017        PMID: 28913826     DOI: 10.1002/cpt.877

Source DB:  PubMed          Journal:  Clin Pharmacol Ther        ISSN: 0009-9236            Impact factor:   6.875


  8 in total

1.  Comprehensive Parent-Metabolite PBPK/PD Modeling Insights into Nicotine Replacement Therapy Strategies.

Authors:  Lukas Kovar; Dominik Selzer; Hannah Britz; Neal Benowitz; Gideon St Helen; Yvonne Kohl; Robert Bals; Thorsten Lehr
Journal:  Clin Pharmacokinet       Date:  2020-09       Impact factor: 6.447

2.  A Physiologically Based Pharmacokinetic and Pharmacodynamic Model of the CYP3A4 Substrate Felodipine for Drug-Drug Interaction Modeling.

Authors:  Laura Maria Fuhr; Fatima Zahra Marok; Maximilian Mees; Felix Mahfoud; Dominik Selzer; Thorsten Lehr
Journal:  Pharmaceutics       Date:  2022-07-15       Impact factor: 6.525

3.  An exposure-response analysis of ponesimod clinical efficacy in a randomized phase III study in patients with relapsing multiple sclerosis.

Authors:  Belén Valenzuela; Per Olsson Gisleskog; Italo Poggesi; Tatiana Sidorenko; Michel Burcklen; Hilke Kracker; Juan Jose Pérez-Ruixo
Journal:  CPT Pharmacometrics Syst Pharmacol       Date:  2022-09-01

4.  First use of cenerimod, a selective S1P1 receptor modulator, for the treatment of SLE: a double-blind, randomised, placebo-controlled, proof-of-concept study.

Authors:  Viktoria Hermann; Anastas Batalov; Svetlana Smakotina; Pierre-Eric Juif; Peter Cornelisse
Journal:  Lupus Sci Med       Date:  2019-11-09

5.  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

6.  Population Pharmacokinetic Analysis of BMS-986166, a Novel Selective Sphingosine-1-Phosphate-1 Receptor Modulator, and Exposure-Response Assessment of Lymphocyte Counts and Heart Rate in Healthy Participants.

Authors:  Sébastien Bihorel; Shalabh Singhal; Diane Shevell; Huadong Sun; Jenny Xie; Shenita Basdeo; Ang Liu; Santanu Dutta; Elizabeth Ludwig; Hannah Huang; Kuan-Ju Lin; Aberra Fura; John Throup; Ihab G Girgis
Journal:  Clin Pharmacol Drug Dev       Date:  2020-10-08

7.  Single-dose of LC51-0255, a selective S1P1 receptor modulator, showed dose-dependent and reversible reduction of absolute lymphocyte count in humans.

Authors:  Sang Won Lee; Inyoung Hwang; Jaeseong Oh; SeungHwan Lee; In-Jin Jang; Kyung-Sang Yu
Journal:  Clin Transl Sci       Date:  2022-01-23       Impact factor: 4.689

8.  First-in-human study of the safety, tolerability, pharmacokinetics and pharmacodynamics of single and multiple oral doses of SAR247799, a selective G-protein-biased sphingosine-1 phosphate receptor-1 agonist for endothelial protection.

Authors:  Luc Bergougnan; Sara Armani; Georg Golor; Agnes Tardat; Olivier Vitse; Fabrice Hurbin; Michel Scemama; Franck Poitiers; David Radzik; Christophe Gaudin; Lionel Hovsepian; Anthony J Muslin; Stephane Kirkesseli; Paul Deutsch; Ashfaq A Parkar
Journal:  Br J Clin Pharmacol       Date:  2020-07-08       Impact factor: 3.716

  8 in total

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