Vertaling van "based on clinical data " (Nederlands → Frans) :

Valturna – a single-pill combination of Tekturna/Rasilez and Diovan (valsartan) – gained US regulatory approval in September based on clinical data showing this medicine offers significantly higher blood pressure reduction than either valsartan or aliskiren alone.
Valturna, un comprimé associant Rasilez/Tekturna et Diovan (valsartan), a obtenu, en septembre, son autorisation de mise sur le marché aux Etats-Unis. Cette décision s'est appuyée sur des données cliniques montrant que ce médicament provoque une baisse nettement plus importante de la pression sanguine que valsartan ou aliskiren seuls.

Tekturna/Rasilez (USD 290 million, +104% lc), the first in a new class of medicines known as direct renin inhibitors to treat high blood pressure, has been growing consistently since its launch in 2007 based on positive clinical data demonstrating its prolonged efficacy in lowering blood pressure for more than 24 hours and superiority in clinical trials over ramipril, a leading ACE inhibitor.
Rasilez/Tekturna (USD 290 millions, +104% en m. l.), est le premier d’une nouvelle classe de médicaments, les inhibiteurs directs de la rénine, traitant l’hypertension.

Gleevec/Glivec (USD 3.9 billion, +12% lc), a targeted therapy for some forms of chronic myeloid leukemia (CML) and gastrointestinal stromal tumors (GIST), achieved sustained double-digit growth based on its leadership position in treating these cancers backed by new clinical data and regulatory approvals.
Glivec/Gleevec (USD 3,9 milliards, +12% en m. l.), traitement ciblé contre certaines formes de leucémie myéloïde chronique (LMC) et de tumeurs stromales gastro-intestinales (GIST), a enregistré une croissance soutenue à deux chiffres, grâce à sa position de leader dans le traitement de ces cancers, étayée par de nouveaux résultats cliniques et par des autorisations de mise sur le marché.

Oncology Gleevec/Glivec (USD 2.9 billion, +12% lc), a targeted therapy for some forms of chronic myeloid leukemia (CML) and gastrointestinal stromal tumors (GIST), has achieved sustained double-digit growth based on its leadership position in treating these cancers backed by new clinical data and regulatory approvals.
Oncologie Glivec/Gleevec (USD 2,9 milliards, +12% en m. l.), traitement ciblé contre certaines formes de leucémie myéloïde chronique (LMC) et de tumeurs stromales gastrointestinales (GIST), a enregistré une croissance soutenue à deux chiffres, grâce à sa position de leader dans le traitement de ces cancers, étayée par de nouveaux résultats cliniques et par des autorisations de mise sur le marché.

Gleevec/Glivec (USD 1.9 billion, +15% lc), a targeted therapy for certain forms of chronic myeloid leukemia (CML) and gastrointestinal stromal tumors (GIST), has achieved sustained double-digit growth based on its leadership position in treating these cancers backed by new clinical data and regulatory approvals.
Glivec/Gleevec (USD 1,9 milliard, +15% en m. l.), traitement ciblé contre certaines formes de leucémie myéloïde chronique (LMC) et les tumeurs stromales gastrointestinales (GIST), a enregistré une croissance à deux chiffres, grâce à sa position de leader dans le traitement de ces maladies, étayée par de nouveaux résultats cliniques et par des autorisations de mise sur le marché.

Gleevec/Glivec (USD 3.7 billion, +15% lc), a targeted therapy for certain forms of chronic myeloid leukemia (CML) and gastrointestinal stromal tumors (GIST), sustained solid double-digit growth in 2008 based on strong clinical data and its status as the leading therapy for these and other life-threatening forms of cancer.
Glivec/Gleevec (USD 3,7 milliards, +15% en m. l.), traitement ciblé contre certaines formes de leucémie myéloïde chronique (LMC) et les tumeurs stromales gastro-intestinales (GIST), a conservé une croissance soutenue à deux chiffres, grâce à d’excellents résultats cliniques et à son statut de traitement de pointe pour ces maladies et d’autres formes de cancer souvent fatales.

Key drivers are clinical data demonstrating its prolonged efficacy in lowering blood pressure for more than 24 hours, and superiority in clinical trials over ramipril, a leading ACE inhibitor (an older class of high blood pressure medicines).
Les facteurs-clés de cette progression sont des données cliniques faisant état de sa capacité à réduire la pression sanguine pendant plus de 24 heures et de sa supériorité, lors d’essais cliniques, sur le ramipril, un inhibiteur important de l’IEC (une catégorie plus ancienne de médicaments hypotenseurs).

Unit cost: €2.53 Costs of interventions in current practice based on Dutch empirical data Cost calculations of interventions in increased implementation program based on Dutch practice guidelines and (for the duration of NRT and bupropion) on international trials (Cochrane meta-analysis) Costs of smoking-related diseases were taken into account, estimates based on Dutch cost-ofillness study that allocated total direct health care costs to diseases.
Unit cost: €2.53 Costs of interventions in current practice based on Dutch empirical data Cost calculations of interventions in increased implementation program based on Dutch practice guidelines and (for the duration of NRT and Buproprion) on international trials (Cochrane meta-analysis) Costs of smoking-related diseases were taken into account, estimates based on Dutch cost-ofillness study that allocated total direct health care costs to diseases.

An example of micro data is a recent transparency in ambulatory supplements as well as in private hospital large-scale European nursing workforce study based on survey data.
79,138 Workforce counts: better dataa on the supply side available, but data on the need side still lacking No indicators of the needs have been defined yet in this report, but the reflection should continue on this topic.

" Compliance with this standard (= GCP) provides public assurance that the rights, safety and well-being of trial subjects are protected, consistent with the principles that have their origin in the Declaration of Helsinki, and that the clinical trial data are credible.‰
ÿ Compliance with this standard (= GCP) provides public assurance that the rights, safety and well-being of trial subjects are protected, consistent with the princinciples that have their origin in the Declaration of Helsinki, and that the clinical trial data are credible. Ÿ