Traduction de «organ rejection based on » (Néerlandais → Français) :

Certican (USD 34 million, +36% cc), a transplantation medicine, is now available in more than 70 countries for use in the prevention of organ rejection based on its immunosuppressive efficacy and side-effect profile.
Aclasta/Reclast (USD 123 millions, +41% tcc) a conservé un rythme élevé de croissance soutenu par les Etats-Unis et par une extension du nombre de pays où il est commercialisé.

Zortress/Certican (USD 35 million, +19% cc), a transplantation medicine to prevent organ rejection in adult kidney and heart transplantation, continues to grow based on its availability in more than 80 countries and its US launch for adult kidney transplantation in April, 2010, under the brand name Zortress and is currently in two Phase III studies with global participation in heart transplantation, and also a worldwide study for liver transplantation.
Certican/Zortress (USD 35 millions, +19% tcc) est un médicament destiné à prévenir le rejet des organes dans les transplantations du rein et du cœur chez l’adulte.

The FDA approved Zortress (everolimus) for the prevention of organ rejection in kidney transplant patients and Tasigna (nilotinib) for newly diagnosed chronic myeloid leukemia.
d’organes chez les patients ayant subi une transplantation du rein et pour Tasigna (nilotinib) contre la leucémie myéloïde chronique dépistée précocement.

Certican/Zortress (USD 36 million, +33% cc) is now available in more than 80 countries to prevent organ rejection in adult kidney transplantation, heart transplantation, or both.
Certican/Zortress (USD 36 millions, +33% tcc), un médicament destiné à prévenir le rejet d’organes dans les transplantations du rein et du cœur chez les adultes, est maintenant disponible dans plus de 80 pays.

In the US, the FDA issued a Complete Response letter in December 2009 for this medicine (under the brand name Zortress) for prevention of organ rejection in adult kidney transplant patients.
Aux Etats-Unis, la FDA a émis, en décembre 2009, une «Complete Response letter» pour ce médicament (sous la marque Zortress) pour la prévention du rejet d'organe chez les transplantés adultes du rein.

Certican Prevention of organ 2011 III rejection – liver DEB025 Hepatitis C 2013 II - Phase III start planned in Q4 2010 Exjade Non transfusion 2011 II dependent Thalassemia HCD122 Hematological tumors ≥2014 I INC424 Myelofibrosis 2011 III - Results from a Phase I/II study published in The New England Journal of Medicine in September showed approximately 75% of myelofibrosis patients receiving INC424 twice-daily experienced rapid reduction in spleen size, which was durable for more than one year of follow-up
INC424 Myélofibrose 2011 III - Les résultats de l’étude de phase I/II publiés en septembre dans The New England Journal of Medicine montrent que 75% env. des malades atteints de myélofibrose et recevant INC424 deux fois par jour ont constaté une diminution rapide de la taille de leur rate, qui s’est maintenue au-delà d’un an de

Certican Prevention of organ 2011 III rejection – liver DEB025 Hepatitis C 2013 II - Phase III start planned in Q4 2010 Exjade Non transfusion 2011 II dependent Thalassemia HCD122 Hematological tumors ≥2014 I INC424 Myelofibrosis 2011 III LBH589 Hodgkin’s lymphoma 2010 II - On track for 2010 submission
Indication potentielle Projet / / domaine Soumissions Phase Mise à jour molécule thérapeutique prévues actuelle BAF312 Sclérose en plaques ≥2014 II - Résultats de phase II attendus au T4 2010 Certican Prévention du rejet d’organe – foie 2011 III

Nucleic acid sequence based amplification Nucleic Acid Amplification Testing Non-heart beating donors National Institute for Biological Standards and Control Optische densiteit Occupational Safety and Health Administration Perazijnzuur Phosphate buffered saline Polymerase chain reaction Perazijnzuur ethanol sterilisatie Positive predictive value Positief predictieve waarde Polyvinyl-pyrrolidon Povidone-iodine Quaternaire ammoniumverbindingen Radio-immunoprecipitatie test Ribonucleic acid Ribonuclease H Respiratoir syncytiaal virus Reverse transcriptase Advisory Committee on the Safety of Blood, Tissues and Organs Sterility assurance level Severe acute respiratory syndrome Median tissue culture infective dose Transcription-mediated amplification Tumor necrosis factor United Kingdom United Kingdom Blood Transfusion Services Ultraviolet Vapour-phase hydrogen peroxide Verenigde Staten Werkgroep infectiepreventie West Nile virus World Health Organization
Morbidity and mortalility weekly report Nucleic acid sequence based amplification Nucleic Acid Amplification Testing National Institute for Biological Standards and Control Occupational Safety and Health Administration Phosphate buffered saline ou tampon phosphate Polymerase chain reaction Stérilisation acide peracétique-éthanol Positive predictive value Polyvinyl-pyrrolidon Povidone-iodine Dérivés de l’ammonium quaternaire Ribonuclease H Reverse transcriptase ou transcriptase inverse Advisory Committee on the Safety of Blood, Tissues and Organs Sterility assurance level Severe acute respiratory syndrome Syndrome d’immunodéficience acquise Median tissue culture infective dose Test d’immunofluorescence indirecte Transcription-mediated amplification Tumor necrosis factor Test de radio-immunoprécipitation United Kingdom United Kingdom Blood Transfusion Services Ultraviolet Vapour-phase hydrogen peroxide Valeur prédictive positive Virus respiratoire syncytial Etats-Unis Werkgroep infectiepreventie ou groupe de travail sur la prévention des infections West Nile virus World Health Organization

Evidence-based practice, Health Services Research; Mental Health Services; Organization and administration
Evidence-based practice , Health Services Research; Mental Health Services; Organization and administration