Vertaling van "regulatory filings " (Nederlands → Frans) :

Regulatory filings are expected this year in pancreatic neuroendocrine tumors (pNET) following data showing Afinitor met the primary endpoint of progression-free survival in a Phase III study of pNET.
A la suite de résultats d’une étude de phase III consacrée aux tumeurs neuroendocrines du pancréas (pTNE) montrant qu’Afinitor satisfaisait au critère principal de survie sans progression de la maladie, des demandes d’autorisation devraient être déposées cette année.

This release contains forward-looking information about an agreement by Pfizer to acquire FoldRx, and about FoldRx’s product candidate tafamidis, its other clinical and preclinical development programs and its technology platform, including their potential benefits, that involves substantial risks and uncertainties. Such risks and uncertainties include, among other things, the satisfaction of conditions to closing the agreement; the uncertainties inherent in research and development; whether and when a new drug application for tafamidis will be filed with the FDA; decisions by regulatory authorities regarding whether and when to approve any drug applications that have been or may be filed for tafamidis and that may be filed for any other product candidates that may be generated by FoldRx’s technology platform as well as their decisions regarding labeling and other matters that could affect the availability or commercial potential of tafamidis and such other product candidates; and competitive developments. A further description of risks and uncertainties can be found in Pfizer’s Annual Report on Form 10-K for the fiscal year ended December 31, 2009 and in its reports on Form 10-Q and Form 8-K.
Such risks and uncertainties include, among other things, the satisfaction of conditions to closing the agreement; the uncertainties inherent in research and development; whether and when a new drug application for tafamidis will be filed with the FDA; decisions by regulatory authorities regarding whether and when to approve any drug applications that have been or may be filed for tafamidis and that may be filed for any other product candidates that may be generated by FoldRx’s technology platform as well as their decisions regarding labeling and other matters that could affect the availability or commercial potential of tafamidis and such other product candidates; and competitive developments.

Afinitor (USD 67 million) continued regulatory submissions with a filing in the EU with the trade name Votubia for patients with subependymal giant cell astrocytomas (SEGA) associated with tuberous sclerosis.
Afinitor (USD 67 millions), les demandes d’autorisation se poursuivent, notamment dans l’UE sous la marque Votubia pour le traitement de l’astrocytome sous épendymaire à cellules géantes associé à une sclérose tubéreuse.

Additionally, Gilenya is currently under regulatory review in the EU, where it was filed in December 2009, and with health authorities worldwide, including Canada, Switzerland, Turkey, Brazil and Australia.
En outre, ce médicament est actuellement examiné par les autorités réglementaires de l’UE, où une demande a été déposée en novembre 2009 ainsi que par les autorités de la santé du monde entier, notamment du Canada, de la Suisse, de la Turquie, du Brésil et de l’Australie.

In December 2009, a regulatory submission was filed in Europe for treatment of visual impairment due to diabetic macular edema (DME).
Une demande d’homologation a été déposée, en décembre 2009, en Europe pour le traitement de la perte de la vision due à l’œdème maculaire diabétique.

D:\mule\mule-standalone-3.4.0\files\work\16\9E59DABC-4982-48C1-8FA8-BAFA0332B5D8\Leaflet (NL) Regulatory Affairs Dept./MSE
D:\mule\mule-standalone-3.4.0\files\work\16\9E59DABC-4982-48C1-8FA8-BAFA0332B5D8\Leaflet (FR) Regulatory Affairs Dept./MSE