Vertaling van "benefit risk and pharmacokinetic " (Nederlands → Frans) :

AGO178 (agomelatine), a once-daily investigational treatment for patients with major depression, will be studied in additional Phase III trials to further explore the benefit/risk and pharmacokinetic profile of this compound.
AGO178 (agomélatine), un traitement investigationnel par prise unique quotidienne contre la dépression sévère, fera l’objet d’une étude dans le cadre d’essais supplémentaires de phase III afin d’explorer plus avant le profil bénéfice/risque et pharmacocinétique de cette molécule.

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.

The study confirmed a significant benefit for Femara versus tamoxifen in reducing the risk of distant metastases and the overall risk of breast cancer recurrence.
Cette étude a confirmé les avantages importants de Femara comparé au tamoxifène pour réduire le risque de métastases distantes et globalement celui de récidive du cancer du sein.

We assess the potential effects of our operations on the environment – and the health and safety of our associates and neighbors – to ensure that the benefits of new products, processes and technologies outweigh any risks.
Nous évaluons toujours les effets possibles de nos activités sur l’environnement – de même que sur la santé et la sécurité de nos collaboratrices et collaborateurs et de ceux qui nous entourent – afin de nous assurer que les bénéfices de nouveaux produits, de nouveaux procédés ou de nouvelles technologies sont supérieurs aux risques potentiels.

The continuous and multidisciplinary product reviews protect and benefit patients as well as manage risks to Novartis as a whole.
Le contrôle de la sécurité de nos produits s’opère de façon continue et multidisciplinaire ; son premier objectif consiste à protéger les malades, mais il représente également, pour Novartis, un outil supplémentaire dans la gestion des risques.

- Dossier for ABF656 at once-everytwo-weeks dosing continues under review in the US; the FDA provided preliminary comments to Human Genome Sciences on the potential risk/benefit of once-every-two-weeks dosing
- Le dossier d’ABF656 comportant une dose unique toutes les 2 semaines est toujours examiné aux Etats-Unis; La FDA a transmis à Human Genome Sciences des commentaires préliminaires au sujet du risque/avantage potentiel de ce

Also supporting the broad expansion have been landmark data first presented in 2008, and published in early 2009 in “The New England Journal of Medicine,” that showed the significant anti-cancer benefit of Zometa in reducing the risk of cancer recurrence or death in premenopausal women with hormone-sensitive, earlystage breast cancer.
Cette large progression a été soutenue par de nouveaux résultats d’une étude pivot présentés initialement en 2008 et publiés début 2009 dans «The New England Journal of Medicine» faisant état des bénéfices anticancer importants du Zometa dans le risque de récidive ou de décès chez les femmes préménopausées atteintes d’un cancer du sein hormono-dépendant précoce.

This release contains forward-looking information about a potential joint venture between Pfizer and Zhejiang Hisun Pharmaceuticals (Hisun) including, among other things, the anticipated benefits there of, that involves substantial risks and uncertainties.
This information contained in this release is as of June 2, 2011, Pfizer assumes no obligation to update forward-looking statements contaiTned in this release as the result of new information or future events or developments. This release contains forward-looking information about a potential joint venture between Pfizer and Zhejiang Hisun Pharmaceuticals (Hisun) including, among other things, the anticipated benefits there of, that involves substantial risks and uncertainties.

This release contains forward-looking information that involves substantial risks and uncertainties regarding Prevenar 13, including its potential benefits; and the success of the AMC project for vaccines.
DISCLOSURE NOTICE: The information contained in this release is as of December 12, 2010. Pfizer assumes no obligation to update forward-looking statements contained in this release as the result of new information or future events or developments.

Diovan has benefited from its status as the only medicine in the ARB class approved to treat high blood pressure, high-risk heart attack survivors and heart failure.
Diovan a bénéficié de son statut de seul médicament de la classe des ARA autorisé pour le traitement de l’hypertension, de survivants d’attaques cardiaques à haut risque et de patients souffrant d’insuffisance cardiaque.