Introduction: Multiple Sclerosis (MS) is an immune-mediated, complex, chronic inflammatory, and neurodegenerative disease of the central nervous system. Among the several therapeutic options developed over the last decade for relapsing MS (RMS), fingolimod, a sphingosine 1-phosphate receptor (S1PR) modulator, was the first oral treatment. The adverse events associated with fingolimod have limited its use in certain populations, thus further stimulating the search for other S1PR modulators. Areas covered: The authors reviewed the English-published literature on ponesimod using the PubMed database. The search terms used were ‘ponesimod’ or ‘ACT-128,800’ and ‘multiple sclerosis.’ Available data on the pharmacological profile of ponesimod and the information on clinical efficacy and safety drawn from clinical trials in comparison with other S1PR modulators are presented and discussed. Expert opinion: Published peer-reviewed data on long-term safety and efficacy are still lacking but have been collected and regulatory authorities expressed a favorable opinion to market access. At present, we believe that ponesimod has little chance of becoming a leading treatment for RMS due to the availability of many alternative options and the timing of market access. Given its favorable risk-benefit and convenience profile, however, ponesimod might become a leading option among S1P receptor modulators used for RMS.
Baldin E., Lugaresi A. (2020). Ponesimod for the treatment of relapsing multiple sclerosis. EXPERT OPINION ON PHARMACOTHERAPY, 21(16), 1955-1964 [10.1080/14656566.2020.1799977].
Ponesimod for the treatment of relapsing multiple sclerosis
Baldin E.Primo
Writing – Original Draft Preparation
;Lugaresi A.
Ultimo
Conceptualization
2020
Abstract
Introduction: Multiple Sclerosis (MS) is an immune-mediated, complex, chronic inflammatory, and neurodegenerative disease of the central nervous system. Among the several therapeutic options developed over the last decade for relapsing MS (RMS), fingolimod, a sphingosine 1-phosphate receptor (S1PR) modulator, was the first oral treatment. The adverse events associated with fingolimod have limited its use in certain populations, thus further stimulating the search for other S1PR modulators. Areas covered: The authors reviewed the English-published literature on ponesimod using the PubMed database. The search terms used were ‘ponesimod’ or ‘ACT-128,800’ and ‘multiple sclerosis.’ Available data on the pharmacological profile of ponesimod and the information on clinical efficacy and safety drawn from clinical trials in comparison with other S1PR modulators are presented and discussed. Expert opinion: Published peer-reviewed data on long-term safety and efficacy are still lacking but have been collected and regulatory authorities expressed a favorable opinion to market access. At present, we believe that ponesimod has little chance of becoming a leading treatment for RMS due to the availability of many alternative options and the timing of market access. Given its favorable risk-benefit and convenience profile, however, ponesimod might become a leading option among S1P receptor modulators used for RMS.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.