Traduction de «been approved in over 20 other » (Néerlandais → Français) :

Extavia, the Novartis-branded version of Betaferon ® /Betaseron ® for relapsing forms of multiple sclerosis, was launched in the US in 2009, and since then has been approved in over 20 other countries.
Extavia, la marque de Novartis de la version de Betaferon ® /Betaseron ® contre les formes cycliques de la sclérose en plaques (SP), a été lancé en 2009 aux Etats-Unis et a été homologué depuis dans plus de vingt autres pays en 2010.

Extavia, the Novartis-branded version of Betaferon ® /Betaseron ® for relapsing forms of multiple sclerosis, was launched in the EU and US in 2009, and has been approved in over 30 countries.
Extavia, la marque de Novartis de la version de Betaferon ® /Betaseron ® contre les formes cycliques de la sclérose en plaques (SP), a été lancé en 2009 dans l’Union européenne et aux Etats-Unis et a été homologué depuis dans plus de trente pays.

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.

Tasigna (USD 109 million, +97% cc) has been growing rapidly through geographic and market expansion with approvals in over 85 countries as a second-line therapy for patients with certain forms of Ph+ CML resistant or intolerant to prior therapy including Gleevec/Glivec.
Tasigna (USD 109 millions, +97% tcc), a affiché une croissance rapide grâce à son expansion dans les pays et les marchés à la suite des autorisations accordées dans plus de 85 pays en tant que traitement de deuxième intention pour les malades atteints de certaines formes de LMC à Ph+ présentant une résistance ou une intolérance aux traitements antérieurs, Glivec/Gleevec inclus.

This biotechnology eye therapy, which is approved in more than 80 countries for “wet” age-related macular degeneration, has now been used in more than 250,000 patients for this disease, a leading cause of blindness in people over age 50.
Ce traitement oculaire issu des biotechnologies, autorisé dans plus de 80 pays contre la forme exsudative de la dégénérescence maculaire liée à l'âge, cause principale de cécité chez les personnes âgées de plus de 50 ans, a été utilisé chez plus de 250 000 malades.

Ilaris, a fully human monoclonal antibody that blocks action of the inflammatory protein interleukin-1 beta, has been launched after receiving first approvals during 2009 in the US, Europe and some other markets for treatment of cryopyrin-associated periodic syndrome (CAPS), a group of rare lifelong auto-inflammatory disorders.
Ilaris, un anticorps monoclonal entièrement humain qui bloque l’action de l’interleukine-1 bêta (IL- 1β), une protéine inflammatoire, a été lancé après avoir obtenu ses premières autorisations en 2009 aux Etats-Unis, en Europe et dans quelques autres marchés pour le traitement du syndrome périodique associé à la cryopirine (CAPS), un groupe de maladies rares auto-inflammatoires tout au long de la vie.

Exforge HCT, the first modern triple hypertension medication, which adds a diuretic in a single pill, was introduced in the US in 2009 and has gained approvals in over 20 countries worldwide.
Exforge HCT, le premier médicament moderne contre l’hypertension associant trois molécules, dont un diurétique, en un seul comprimé a été introduit en 2009 aux Etats-Unis et a été depuis autorisé dans plus de vingt pays.

Extavia, the Novartis-branded version of Betaferon ® /Betaseron ® for relapsing forms of multiple sclerosis, was launched in the US in 2009, and in over 20 other countries, including Canada and Russia, in 2010.
Extavia, la marque de Novartis de la version de Betaferon ® /Betaseron ® contre les formes cycliques de la sclérose en plaques (SP), a été lancé en 2009 aux Etats-Unis et dans plus de vingt autres pays en 2010, dont le Canada et la Russie.