Radiprodil, a NR2B negative allosteric modulator, from bench to bedside in infantile spasm syndrome
Abstract Objective Infantile spasm syndrome (ISS) is an epileptic encephalopathy without established treatment after the failure to standard of care based on steroids and vigabatrin. Converging lines of evidence indicating a role of NR2B subunits of the N‐methyl‐D‐aspartate (NMDA) receptor on the on...
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doaj-6e28defa096e430da2342590d5729c982021-05-02T14:08:22ZengWileyAnnals of Clinical and Translational Neurology2328-95032020-03-017334335210.1002/acn3.50998Radiprodil, a NR2B negative allosteric modulator, from bench to bedside in infantile spasm syndromeStéphane Auvin0Blandine Dozières‐Puyravel1Andreja Avbersek2David Sciberras3Jo Collier4Karine Leclercq5Pavel Mares6Rafal M. Kaminski7Pierandrea Muglia8Service de Neurologie Pédiatrique Hôpital Robert Debré Paris FranceService de Neurologie Pédiatrique Hôpital Robert Debré Paris FranceUCB Pharma Braine‐L’Alleud BelgiumUCB Pharma Braine‐L’Alleud BelgiumUCB Pharma Braine‐L’Alleud BelgiumUCB Pharma Braine‐L’Alleud BelgiumInstitute of Physiology The Czech Academy of Sciences Prague Czech RepublicUCB Pharma Braine‐L’Alleud BelgiumUCB Pharma Braine‐L’Alleud BelgiumAbstract Objective Infantile spasm syndrome (ISS) is an epileptic encephalopathy without established treatment after the failure to standard of care based on steroids and vigabatrin. Converging lines of evidence indicating a role of NR2B subunits of the N‐methyl‐D‐aspartate (NMDA) receptor on the onset of spams in ISS patients, prompted us to test radiprodil, a negative allosteric NR2B modulator in preclinical seizure models and in infants with ISS. Methods Radiprodil has been tested in three models, including pentylenetetrazole‐induced seizures in rats across different postnatal (PN) ages. Three infants with ISS have been included in a phase 1b escalating repeated dose study. Results Radiprodil showed the largest protective seizure effects in juvenile rats (maximum at PN12, corresponding to late infancy in humans). Three infants resistant to a combination of vigabatrin and prednisolone received individually titrated doses of radiprodil for up to 34 days. Radiprodil was safe and well tolerated in all three infants, and showed the expected pharmacokinetic profile. One infant became spasm‐free and two showed clinical improvement without reaching spasm‐freedom. After radiprodil withdrawal, the one infant continued to be spasm‐free, while the two others experienced seizure worsening requiring the use of the ketogenic diet and other antiepileptic drugs. Interpretation Radiprodil showed prominent anti‐seizure effect in juvenile animals, consistent with the prevalent expression of NR2B subunit of the NMDA receptor at this age in both rodents and humans. The clinical testing, although preliminary, showed that radiprodil is associated with a good safety and pharmacokinetic profile, and with the potential to control epileptic spasms.https://doi.org/10.1002/acn3.50998 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Stéphane Auvin Blandine Dozières‐Puyravel Andreja Avbersek David Sciberras Jo Collier Karine Leclercq Pavel Mares Rafal M. Kaminski Pierandrea Muglia |
spellingShingle |
Stéphane Auvin Blandine Dozières‐Puyravel Andreja Avbersek David Sciberras Jo Collier Karine Leclercq Pavel Mares Rafal M. Kaminski Pierandrea Muglia Radiprodil, a NR2B negative allosteric modulator, from bench to bedside in infantile spasm syndrome Annals of Clinical and Translational Neurology |
author_facet |
Stéphane Auvin Blandine Dozières‐Puyravel Andreja Avbersek David Sciberras Jo Collier Karine Leclercq Pavel Mares Rafal M. Kaminski Pierandrea Muglia |
author_sort |
Stéphane Auvin |
title |
Radiprodil, a NR2B negative allosteric modulator, from bench to bedside in infantile spasm syndrome |
title_short |
Radiprodil, a NR2B negative allosteric modulator, from bench to bedside in infantile spasm syndrome |
title_full |
Radiprodil, a NR2B negative allosteric modulator, from bench to bedside in infantile spasm syndrome |
title_fullStr |
Radiprodil, a NR2B negative allosteric modulator, from bench to bedside in infantile spasm syndrome |
title_full_unstemmed |
Radiprodil, a NR2B negative allosteric modulator, from bench to bedside in infantile spasm syndrome |
title_sort |
radiprodil, a nr2b negative allosteric modulator, from bench to bedside in infantile spasm syndrome |
publisher |
Wiley |
series |
Annals of Clinical and Translational Neurology |
issn |
2328-9503 |
publishDate |
2020-03-01 |
description |
Abstract Objective Infantile spasm syndrome (ISS) is an epileptic encephalopathy without established treatment after the failure to standard of care based on steroids and vigabatrin. Converging lines of evidence indicating a role of NR2B subunits of the N‐methyl‐D‐aspartate (NMDA) receptor on the onset of spams in ISS patients, prompted us to test radiprodil, a negative allosteric NR2B modulator in preclinical seizure models and in infants with ISS. Methods Radiprodil has been tested in three models, including pentylenetetrazole‐induced seizures in rats across different postnatal (PN) ages. Three infants with ISS have been included in a phase 1b escalating repeated dose study. Results Radiprodil showed the largest protective seizure effects in juvenile rats (maximum at PN12, corresponding to late infancy in humans). Three infants resistant to a combination of vigabatrin and prednisolone received individually titrated doses of radiprodil for up to 34 days. Radiprodil was safe and well tolerated in all three infants, and showed the expected pharmacokinetic profile. One infant became spasm‐free and two showed clinical improvement without reaching spasm‐freedom. After radiprodil withdrawal, the one infant continued to be spasm‐free, while the two others experienced seizure worsening requiring the use of the ketogenic diet and other antiepileptic drugs. Interpretation Radiprodil showed prominent anti‐seizure effect in juvenile animals, consistent with the prevalent expression of NR2B subunit of the NMDA receptor at this age in both rodents and humans. The clinical testing, although preliminary, showed that radiprodil is associated with a good safety and pharmacokinetic profile, and with the potential to control epileptic spasms. |
url |
https://doi.org/10.1002/acn3.50998 |
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