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Kusajili – Centralise les essais cliniques mondiaux
Résultat
de votre recherche span> par promoteur : Novartis Pharma
Femme et Homme Max 99 ans
Novartis Pharma Services AG
MAJ Il y a 5 ans
Efficacy and safety of QGE031 versus placebo and Omalizumab in patients aged 18-75 years with asthma
Responder rate compared to placebo
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Essai clos aux inclusions
Plus d'informations
Femme et Homme Max 99 ans
Novartis Pharma Services AG
MAJ Il y a 5 ans
Safety and efficacy of BEZ235 in patients with pancreatic neuroendocrine tumors (pNET)
To estimate the efficacy of BEZ235 in adult patients with advanced (unresectable or metastatic) pNET (PFS)
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Essai clos aux inclusions
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Femme et Homme Max 99 ans
Novartis Pharmaceuticals UK Ltd
MAJ Il y a 5 ans
A twelve week, randomized, double-blind, parallel-group multicentre study to evaluate the efficacy and safety of the combination of aliskiren/ramipril/amlodipine (300/10/10mg), compared to the combinations of ramipril/amlodipine (10/10mg) and aliskiren/amlodipine (300/10mg) in patients with essential hypertension and metabolic syndrome not adequately responsive to amlodipine 10mg
The primary objectives of this study are: 1. To demonstrate that the combination of aliskiren / ramipril / amlodipine (300/10/10 mg) has superior efficacy compared to the combinations of ramipril / am...
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Essai clos aux inclusions
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Femme et Homme Max 99 ans
Novartis Pharma Services AG
MAJ Il y a 5 ans
A randomized, double-blind, parallel-group, cross-over, 4-period, 4 treatment, within-subject placebo-controlled study to assess the renoprotective effect of renin inhibition with Aliskiren as an alternative to irbesartan in Type 2 patients with incipient/overt diabetic nephropathy
• To investigate whether renin-inhibition using Aliskiren 300 mg daily could be a treatment alternative to the angiotensin II receptor antagonist Irbesartan 300 mg with an equivalent potential for re...
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Essai clos aux inclusions
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Femme et Homme Max 99 ans
Novartis Pharma GmbH
MAJ Il y a 5 ans
A 12 week treatment, open-label, multicenter study to investigate the efficacy and safety of valsartan 160-320 mg with regard to effects on lipid subfractions in hypertensive patients with metabolic syndrome
To demonstrate that valsartan 320 mg has a positive effect on small, dense LDL subfractions (LDL 5+6) in hypertensive patients with metabolic syndrome after 12 weeks of treatment.
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Essai clos aux inclusions
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Femme et Homme Max 99 ans
Novartis Pharma AG
MAJ Il y a 5 ans
A study to assess the effect of 3 different doses of LIK066 in patients with type 2 diabetes and heart failure, compared to the effect of placebo or empagliflozin
To assess the dose-response relationship of three dose regimens of LIK066 as measured by the change from baseline in NT-proBNP relative to placebo after 12 weeks of treatment in T2DM patients with HF
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unknown
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Femme et Homme Max 99 ans
Novartis Pharma GmbH
MAJ Il y a 5 ans
Multicenter randomized open-label three-arms controlled 12 months clinical proof of concept study to evaluate efficacy and safety of Ranibizumab alone or in combination with laser treatment vs. laser treatment alone in Proliferative Diabetic Retinopathy
Change of area of neovascularizations as measured by Fluorescein Angiography at month 12 (difference to baseline value).
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unknown
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Femme et Homme Max 99 ans
Novartis Pharma Services AG
MAJ Il y a 5 ans
The study is to gather evidence of LFG316 efficacy in treatment of transplant associated microangiopathy (TAM) after hematopoetic precursor cell transplantation
To assess the hematological response rate in patients with TAM receiving LFG316 compared to standard of care (SoC)
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unknown
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Femme et Homme Max 99 ans
Novartis Pharma GmbH
MAJ Il y a 5 ans
An uncontrolled, multicenter 12 month long term study on skin reconstitution with Elidel® (pimecrolimus) 1% cream in adult patients with atopic eczema and corticosteroid induced skin damage
To investigate the reconstitution of steroid damaged skin with pimecrolimus 1% cream by the decrease of the Dermatophot® score from baseline to end of the study.
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Essai clos aux inclusions
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Femme et Homme Max 99 ans
Novartis Pharma Services AG
MAJ Il y a 5 ans
Study to allow access to imatinib for patients who are on imatinib treatment in a Novartis-sponsored study and are benefiting from the treatment as judged by the investigator
To evaluate long term safety data (SAEs and AEs).
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unknown
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