Vertaling van "vision with lucentis in " (Nederlands → Frans) :

Two clinical studies recently confirmed rapid and sustained improvement in vision with Lucentis in another debilitating eye condition, visual impairment due to diabetic macular edema (DME), currently under regulatory review in the EU.
Deux études cliniques récentes ont confirmé que Lucentis améliorait rapidement et durablement la vision dans une autre affection invalidante de l'œil due à l’œdème maculaire diabétique.

Lucentis (USD 377 million, +29% cc) has maintained strong growth reflecting its position as the only approved medicine to significantly improve vision in patients with wet age-related macular degeneration (AMD).
Lucentis (USD 377 millions, +29% tcc) a poursuivi sa forte croissance, car il est le seul médicament autorisé qui améliore de façon importante la vision des malades atteints de la forme exsudative de la dégénérescence maculaire liée à l’âge (DMLA).

Lucentis (USD 398 million, +22% cc) maintained strong growth reflecting its position as the only approved medicine to significantly improve vision in patients with wet age-related macular degeneration (AMD).
Lucentis (USD 398 millions, +22% tcc) a poursuivi sa forte croissance, car il est le seul médicament autorisé qui améliore de façon importante la vision des malades atteints de la forme exsudative de la dégénérescence maculaire liée à l’âge (DMLA).

Lucentis is the only treatment proven to maintain and improve vision in patients with “wet” age-related macular degeneration, a leading cause of blindness in people over age 50.
Lucentis est le seul traitement à avoir la capacité de conserver et d’améliorer la vision de patients souffrant de la forme exsudative de la dégénérescence maculaire liée à l'âge, cause principale de cécité chez les personnes âgées de plus de 50 ans.

Lucentis (USD 523 million, +42% lc), a biotechnology eye therapy approved in more than 80 countries, generated ongoing dynamic growth in Europe, Latin America, Japan and key emerging markets based on its status as the only treatment proven to maintain and improve vision in patients with “wet” age-related macular degeneration, a leading cause of blindness in people over age 50.
Lucentis (USD 523 millions, +42% en m. l.), traitement biotechnologique des yeux autorisé dans plus de 80 pays, a enregistré une croissance dynamique et continue en Europe, en Amérique latine, au Japon et dans des marchés émergents clés. Il est le seul traitement à avoir prouvé sa capacité de conserver et d’améliorer la vision chez des patients atteints de dégénération maculaire «humide», principale cause de cécité chez les personnes âgées de plus de 50 ans.

Late-stage clinical trials are underway to assess the benefits of Lucentis in patients with certain forms of diabetic macular edema.
Des essais cliniques en phase avancée sont en cours afin d'évaluer les bénéfices de Lucentis chez les malades souffrant de certaines formes d’œdème maculaire diabétique.

These include a historic five regulatory approvals to date in Japan for Rasilez, Tasigna, Xolair, Co-Dio and Lucentis, with regulatory decisions pending for Exforge and Galvus in the world’s second-largest pharmaceuticals market.
Celles-ci comprennent cinq autorisations de mise sur le marché au Japon, qui est le deuxième des plus importants marchés pharmaceutiques du monde, pour Rasilez, Tasigna, Xolair, Co-Dio et Lucentis, tandis que deux sont en suspens pour Exforge and Galvus.

Compliance with the European directives on electronic submissions Compliance with the European directives requires a number of objectives to be achieved: ●● Arriving at a functional vision of communication standards with EMEA and the Member States in partnership with the industry and in line with European legislation ●● Standard project management, with important steps that are sponsored/supported by the Member States: first developing an IT infrastructure and then starting on a highly secure network followed by so-called “proofs of concept” in each field ●● Success depends above all on the FAHMP’s
Compliance with the European directives on electronic submissions Compliance with the European directives requires a number of objectives to be achieved: ●● Arriving at a functional vision of communication standards with EMEA and the Member States in partnership with the industry and in line with European legislation ●● Standard project management, with important steps that are sponsored/supported by the Member States: first developing an IT infrastructure and then starting on a highly secure network followed by so-called “proofs of concept” in each field ●● Success depends above all on the FAHMP’s

Central to this endeavour are the six key factors which represent the FAMHP’s vision and ambition: ●● Recognition at national, European and international level ●● Developing partnerships with the healthcare
Central to this endeavour are the six key factors which represent the FAMHP’s vision and ambition: ●● Recognition at national, European and international level ●● Developing partnerships with the healthcare

In consultation with the Central Working Group, six key factors were determined that reflect the vision of the FAMHP.
In consultation with the Central Working Group, six key factors were determined that reflect the vision of the FAMHP.