Vertaling van "potential benefits " (Nederlands → Frans) :

TERMINOLOGIE

afwijkend(e) | elektro-oculogram [EOG] | afwijkend(e) | elektromyogram [EMG] | afwijkend(e) | elektroretinogram [ERG] | afwijkend(e) | respons op zenuwstimulatie | afwijkend(e) | visually evoked potential [VEP]
Anomalies (de):électromyogramme [EMG] | électro-oculogramme [EOG] | électrorétinogramme [ERG] | potentiels évoqués visuellement | réponse à une stimulation nerveuse

potentiëring | versterking
potentiation/potentialisation | augmentation de l'action d'un médicament par l'absorption d'un second

potentie | kracht
1) puissance sexuelle - 2) efficacité | 1) puissance sexuelle - 2) d'un médicament

IN-CONTEXT TRANSLATIONS

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.

Studies are underway to review potential benefits in other tumor types.
Des études sont en cours afin de déterminer les bénéfices anticancer potentiels de ce médicament dans d’autres types de tumeurs.

Tekturna/Rasilez (USD 119 million, +117% lc), the first new type of high blood pressure medicine in more than a decade, has accelerated its growth pace thanks to an increasing body of data affirming its ability to reduce blood pressure for more than 24 hours, its potential benefits for organ protection, and its consistent superiority in clinical trials over ramipril, a leading ACE inhibitor (another class of high blood pressure medicines).
Rasilez/Tekturna (USD 119 millions, +117% en m. l.), premier médicament d’un nouveau type contre l’hypertension depuis plus d’une décennie, a enregistré une accélération de sa croissance grâce à une masse grandissante de données faisant état de sa capacité à réduire la pression sanguine pendant plus de 24 heures, de ses bénéfices potentiels dans la protection des organes et de sa supériorité constante, manifestée lors des essais cliniques, sur le ramipril, un inhibiteur de l’IEC (une autre classe de médicaments hypotenseurs).

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.

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.

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.

Two US regulatory submissions completed in late 2009 – Tasigna (cancer) and Gilenia (FTY720, multiple sclerosis) – were recognized in the first quarter of 2010 for their potential patient benefits.
Deux demandes d’homologation ont été déposées fin 2009 aux Etats-Unis pour Tasigna (cancer) et Gilenia (FTY720, sclérose en plaques). Les bénéfices potentiels de ces médicaments pour les malades ont été reconnus au premier trimestre 2010.

- 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

Studies are underway to review potential anti-cancer benefits in other tumor types.
Des études sont en cours afin de déterminer les bénéfices anticancer potentiels de ce médicament dans d’autres types de tumeurs.