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Kusajili – Centralise les essais cliniques mondiaux
Résultat
de votre recherche span> par promoteur : Bayer HealthCare AG
Homme Max 99 ans
Bayer HealthCare AG
MAJ Il y a 5 ans
A randomized, explorative, double-blind, double-dummy, multi-center, parallel group study to assess sustainable efficacy of once daily vardenafil (10 mg) for 12 and 24 weeks versus vardenafil PRN in men with mild or mild to moderate erectile dysfunction
The objective of this study is to explore the prophylactic (prophylaxis of deterioration) or curative efficacy and safety of long-term (12 and 24 weeks) daily administration of vardenafil therapy (adm...
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Essai clos aux inclusions
Plus d'informations
Femme et Homme Max 99 ans
Bayer HealthCare AG
MAJ Il y a 5 ans
Study to investigate safety, tolerability, pharmacodynamics and pharmacokinetic properties of BAY 63-2521 after dosing of a 2 mg tablet in 20 patients with Raynaud’s phenomenon (RP)
The primary objective of the study is to investigate the safety, tolerability and pharmacodynamics of a single oral dose of BAY 63-2521 administered in patients suffering from Raynaud’s phenomenon
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Essai clos aux inclusions
Plus d'informations
Femme et Homme Max 99 ans
Bayer HealthCare AG
MAJ Il y a 5 ans
Randomized, double-blind, placebo-controlled, parallel group study of vardenafil 10 mg twice daily to assess the effect on urodynamics in patients with Overactive Bladder (detrusor overactivity)
To determine the therapeutic effect of vardenafil on Overactive Bladder by means of urodynamic measurements (filling cystometry and pressure flow investigations). In addition, a micturition diary wil...
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unknown
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Femme et Homme Max 99 ans
Bayer HealthCare AG
MAJ Il y a 5 ans
Refametinib given to patients with unresectable or metastatic HCC carrying a RAS mutation
The primary objective is to evaluate the efficacy of refametinib in patients with KRAS or NRAS mutant unresectable or metastatic HCC.
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Essai clos aux inclusions
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Femme et Homme Max 99 ans
Bayer HealthCare AG
MAJ Il y a 5 ans
Reduced-dosed rivaroxaban and standard-dosed rivaroxaban versus aspirin in the long-term prevention of blood clots from reccuring in the leg or lung
The primary efficacy objective is to evaluate whether rivaroxaban, in doses of 10 mg or 20 mg, is superior to acetylsalicylic acid (ASA) 100 mg in the prevention of the primary efficacy outcome (i.e. ...
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unknown
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Femme Max 99 ans
Bayer HealthCare AG
MAJ Il y a 5 ans
Single-center, open-label, uncontrolled study to investigate the effects of the transdermal contraceptive patch containing 0.55 mg ethinylestradiol and 2.1 mg gestodene (material no. 80876395) on the endometrium in a 21-day regimen for 13 cycles in 80 healthy women
The primary objective of this study is to investigate the effect of the transdermal contraceptive patch (material no. 80876395, FC Patch Low containing 0.55 mg EE and 2.1 mg GSD) on the endometrium.
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Essai clos aux inclusions
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Femme et Homme Max 99 ans
Bayer HealthCare AG
MAJ Il y a 5 ans
A study investigating the efficacy and safety of copanlisib versus placebo inpatients with rituximab-refratory indolent non-Hodgkin's lymphoma. Copanlisib nell’iNHL di Fase III refrattario a rituximab
to investigate whether copanlisib as monotherapy is superior to placebo in prolonging progression-free survival (PFS) in patients with rituximab-refractory iNHL who have received two or more prior lin...
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unknown
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Homme Max 99 ans
Bayer HealthCare AG
MAJ Il y a 5 ans
A clinical trial investigating safety and efficacy of a long-acting factor VIII in severe hemophila A Studio clinico per valutare sicurezza ed efficacia di un fattore VIII a lunga emivita nell'emofilia A grave
• To assess the efficacy of BAY 94-9027 in prevention and treatment of bleeding at different infusion schedules Part B: Major surgery using BAY 94-9027 • To assess the safety and efficacy of BAY 94-...
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unknown
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Femme et Homme Max 99 ans
Bayer HealthCare AG
MAJ Il y a 5 ans
A study to test the effectiveness of a tablet containing both Nifedipine and Candesartan Cilexetil in adults with high blood pressure whose blood pressure is not well controlled with tablets containing Nifedipine
The primary objective is to demonstrate the superior efficacy of the FDC of nifedipine GITS and candesartan cilexetil compared to nifedipine GITS monotherapy in subjects with essential hypertension no...
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Essai clos aux inclusions
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Femme et Homme Max 99 ans
Bayer HealthCare AG
MAJ Il y a 5 ans
A Phase III randomized, double-blind, placebo-controlled study of sorafenib as adjuvant treatment for hepatocellular carcinoma after surgical resection or local ablation
The Primary efficacy objective is to compare Recurrence Free Survival (RFS) in the patients treated with sorafenib vs placebo after receiving potentially curative treatment with surgical resection or ...
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Essai clos aux inclusions
Plus d'informations
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