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NanoPass Technologies accorde une licence commerciale à Janssen Pharmaceuticals, Inc. pour l'utilisation de son dispositif MicronJet


News provided by

NanoPass Technologies LTD.

Nov 30, 2012, 03:00 ET

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NES ZIONA, Israel, November 30, 2012 /PRNewswire/ --

NanoPass Technologies Ltd. (« NanoPass »), société pionnière en matière de solutions d'administration intradermique pour les vaccins, a annoncé aujourd'hui avoir conclu un accord de licence concernant MicronJet®, son dispositif d'administration par micro-aiguille, avec Janssen Pharmaceuticals, Inc. (JPI) pour plusieurs vaccins.  

L'accord de licence fournira à Janssen l'autorisation exclusive d'utiliser le dispositif dans ses programmes de vaccination contre la grippe saisonnière et pour d'autres vaccins. Les conditions financières n'ont pas été divulguées.  

Yotam Levin, président-directeur général de NanoPass, a déclaré : « Nous sommes ravis de conclure cet accord de licence avec Janssen, une compagnie pharmaceutique de premier plan. Nous voyons une opportunité significative d'améliorer l'immunogénicité et/ou de réduire les doses de vaccination en combinant l'approche de notre dispositif avec les vaccins de Crucell. Cet accord avec Janssen constitue une étape décisive en vue d'une acceptation du marché dans son ensemble. »

Le Dr Richard Kenney, Directeur médical chez Crucell, société affiliée de Janssen, a déclaré : « L'association du dispositif NanoPass MicronJet600 à la technologie de vaccin virosomal contre la grippe de Crucell a le potentiel de changer la réponse immunitaire qualitative pour offrir des bienfaits qu'on ne peut prédire. Une vaccination efficace des personnes âgées est nécessaire de toute urgence ; nous espérons qu'il s'agit de la première étape vers l'élaboration d'un vaccin amélioré. »

À propos de NanoPass Technologies Ltd.

NanoPass a réalisé plusieurs études sur la grippe saisonnière ainsi que la première étude sur le vaccin intradermique de la grippe pandémique H1N1 au monde, démontrant une immunogénicité équivalente ou supérieure à l'administration intramusculaire standard en utilisant seulement 20 % de la dose [i,ii,iii]. La société est soutenue par d'importants investisseurs, dont IHCV, Ofer Hi-Tech, DPartners, WFD Ventures et ‎Elcam Medical.‎

À propos de MicronJet600

MicronJet est un dispositif à micro-aiguille pour l'administration intradermique de vaccins et médicaments, permettant une administration cohérente, simple et quasi-indolore de produits thérapeutiques directement dans la peau. MicronJet a prouvé son efficacité et son innocuité pour divers usages, y compris avec les vaccins de la grippe et l'insuline. La commercialisation de MicronJet est approuvée dans divers territoires, et notamment les États-Unis, pour une utilisation par les professionnels de la santé dans le cadre d'une administration intradermique (voir l'étiquette).

i Hung IFN, Levin Y, To KK. Quantitative and ‎qualitative analysis of antibody response after dose sparing intradermal 2009 H1N1 vaccination.‎ Vaccine (Analyse quantitative et qualitative de la réponse des anticorps après vaccination intradermique à dose parcimonieuse contre le virus H1N1 en 2009. Vaccin). 2012;30(17):2707-8.

ii Van Damme P, Oosterhuis-Kafeja F, Van der Wielen M et al. Safety and efficacy of a novel microneedle device for dose sparing intradermal influenza vaccination in healthy adults. Vaccine (Innocuité et efficacité d'un nouveau dispositif à micro-aiguille pour la vaccination intradermique à dose parcimonieuse chez des adultes en bonne santé. Vaccin). 2009;27(3):454-9.

iii. Hung IFN, Levin Y, To KWW, Chan KH, Zhang AJ, Li P, Li C, Xu T, Wong TY et Yuen KY. Dose sparing intradermal trivalent influenza (2010/2011) vaccination overcomes reduced immunogenicity of the 2009 H1N1 strain. Vaccine (La vaccination intradermique trivalente à dose parcimonieuse contre la grippe (2010/2011) surmonte l'immunogénicité réduite de la souche de H1N1 de 2009. Vaccin). In Press.2012.

Contact :
Yotam Levin, PDG :
+972-523-392727
[email protected]

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