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Kusajili – Centralise les essais cliniques mondiaux
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de votre recherche par promoteur : NOVARTIS
Femme et Homme Max 99 ans
NOVARTIS FARMA
MAJ Il y a 4 ans
Multicenter, randomized, open-label trial to evaluate the safety, tolerability and efficacy of two regimens of Everolimus plus Neoral, given according different blood target levels, in de novo renal transplant recipients Everest the upper target EVErolimus RandomizEd STudy
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Essai clos aux inclusions
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Femme et Homme Max 99 ans
NOVARTIS FARMA
MAJ Il y a 4 ans
A randomized, multi-center, parallel-group, open-label study to evaluate the therapeutical benefit of an initially intensified dosing regimen of Myfortic vs. a standard dosing regimen of Myfortic in combination with Neoral and Corticosteroids in de novo renal transplant patients Studio multicentrico, randomizzato, in aperto, a gruppi paralleli, per valutare l'efficacia di Myfortic a dose inizialmente intensificata in confronto a Myfortic a dose normale, in pazienti con trapianto di rene de novo in terapia con Neoral e corticosteroidi
To evaluate therapeutic benefit by comparing the efficacy defined as the proportion of patients with treatment failure (biopsy proven acute rejection, graft loss or death) at 6 month post transplant ...
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Femme et Homme Max 99 ans
NOVARTIS FARMA
MAJ Il y a 4 ans
A 36 week, randomized, double-blind, multi-center, parallel group study comparing the efficacy and safety of aliskiren in combination with losartan compared to losartan on the regression of left ventricular hypertrophy in overwiight patients with essential hypertension
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Femme et Homme Max 99 ans
NOVARTIS FARMA
MAJ Il y a 4 ans
A Multicenter, Randomized, Double-Blind, Active Controlled Study to Compare the Effect of 24 Weeks Treatment with Vildagliptin 100 mg qd or Metformin 1500 mg daily in Elderly Drug Na ve Patients with Type 2 Diabetes
To demonstrate the efficacy of vildagliptin in elderly drug na ve patients with type 2 diabetes by testing the hypothesis that the hemoglobin A1c HbA1c reduction with vildagliptin 100 mg qd is not ...
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Femme et Homme Max 99 ans
NOVARTIS FARMA
MAJ Il y a 4 ans
To compare the effectiveness and safety of indacaterol with salmeterol /fluticasone propionate treatment in patients with moderate chronic obstructive pulmonary disease who, on entry to the study are being treated with salmeterol /fluticasone propionate Studio per confrontare l'efficacia e la sicurezza di indacaterolo con salmeterolo / fluticasone propionato nel trattamento di pazienti con con broncopneumopatia cronica ostruttiva di grado moderato
To compare the effectiveness and safety of indacaterol with salmeterol /fluticasone propionate treatment in patients with moderate chronic obstructive pulmonary disease who, on entry to the study ar...
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Essai clos aux inclusions
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Femme et Homme Max 99 ans
NOVARTIS FARMA
MAJ Il y a 4 ans
PHASE II STUDY OF IMATINIB MESYLATE IN CHORDOMA
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Femme et Homme Max 99 ans
NOVARTIS FARMA
MAJ Il y a 4 ans
A phase II study to evaluate the efficacy and safety of the investigational compound AUY922 in combination with trastuzumab as second-line treatment in patients with HER2-positive advanced gastric cancer Studio di fase II per valutare l'efficacia e la sicurezza di AUY922 in associazione con trastuzumab come trattamento di seconda linea nei pazienti con carcinoma gastrico HER2-positivo in stadio avanzato
To assess the preliminary efficacy of AUY922 in combination with trastuzumab standard therapy, using Objective Response Rate (ORR), as per investigator, in advanced HER2+ gastric cancer patients pro...
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Femme et Homme Max 99 ans
NOVARTIS FARMA
MAJ Il y a 4 ans
Early vs.delayed EVERolimus in de novo HEART transplant recipients: optimozation of the safety/efficacy profile (EVERHEART Study)
The primary objective of the study is to compare the 6-month cumulative incidence of the safety composite endpoint of wound healing complications related to initial transplant surgery, pleural/pericar...
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Femme et Homme Max 99 ans
NOVARTIS FARMA
MAJ Il y a 4 ans
An open-label, two-period, multi-center, single dose study to assess the pharmacokinetics of AEB071 in de novo liver transplant patients
Primary objective(s) To evaluate the pharmacokinetics of AEB071 and primary metabolite, AEE800, in liver transplant patients in the immediate post transplant period To evaluate the safety and tole...
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Femme et Homme Max 99 ans
NOVARTIS FARMA
MAJ Il y a 4 ans
efficacy, safety and tolerability of AQW051 in reducing L-dopa induced dyskinesias in Parkinson's patients with moderate to severe L-dopa induced dyskinesias l’efficacia, la sicurezza e la tollerabilita' di AQW051 nella riduzione delle discinesie indotte da L-dopa in pazienti affetti da malattia di Parkinson con discinesie indotte da L-dopa da moderate a severe
• To assess the anti-dyskinetic efficacy of multiple doses of AQW051 in Parkinson's patients with moderate to severe L-dopa induced dyskinesias using the modified Abnormal Involuntary Movement Scale...
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