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Kusajili – Centralise les essais cliniques mondiaux
Résultat
de votre recherche par promoteur : Bayer HealthCare
Femme et Homme Max 99 ans
Bayer HealthCare AG
MAJ Il y a 4 ans
Estudio fase II no controlado, abierto en pacientes con adenocarcinoma metastásico de colon o recto, que están recibiendo quimioterapia de primera línea con mFOLFOX6 (oxaliplatino/acido folínico/5-fluorouracilo [5-FU]) en combinación con regorafenib (An uncontrolled, open-label, phase II study in subjects with metastatic adenocarcinoma of the colon or rectum who are receiving first line chemotherapy with mFOLFOX6 (oxaliplatin/ folinic acid/5-fluorouracil [5-FU]) in combination with regorafenib)
Tasa de respuesta objetiva (TRO) evaluada centralmente
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unknown
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Femme et Homme Max 99 ans
Bayer HealthCare AG
MAJ Il y a 4 ans
Oral Direct Factor Xa Inhibitor BAY 59-7939 in Patients with acute symptomatic Deep Vein Thrombosis ODIXa-DVT A prospective, randomized, multinational, multicenter, partially blinded, parallel-group, open-label active comparator controlled phase II Dose Finding and Proof of Principle Trial
The objectives of this Phase II dose finding trial are to assess the efficacy and safety of BAY 59-7939 for the treatment of acute symptomatic proximal deep vein thrombosis (objectively confirmed by c...
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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 4 ans
A Phase III randomized, placebo-controlled study of sorafenib in patients with advanced hepatocellular carcinoma ** Amendment 1 Version 2.0 of December 13th 2004 is also included
Main objective: To evaluate safety, efficacy, PRO, and population PK of sorafenib versus placebo in patients with advanced HCC. Primary efficacy objectives: • Efficacy in patients treated with soraf...
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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 4 ans
Study to evaluate the safety and pharmacokinetics of ciprofloxacin following inhalation of ciprofloxacin dry powder for inhalation administered to pediatric patients with cystic fibrosis aged 12-17 years
Primary objective of the study is to investigate the safety and tolerability of inhaled ciprofloxacin given as single inhalation dose to pediatric CF patients.
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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 4 ans
A prospective, randomized, double dummy, double blind, multinational, multicenter trial comparing the safety and efficacy of sequential (intravenous/oral) moxifloxacin 400 mg once daily to intravenous piperacillin/tazobactam 4.0/0.5 g every 8 hours followed by oral amoxicillin/clavulanic acid tablets 875/125 mg every 12 hours for the treatment of subjects with complicated skin and skin structure infections (RELIEF Study)
The objective of this study is to compare the efficacy and safety of two sequential (IV/PO) treatment regimens for the treatment of adult subjects with cSSSIs: • Moxifloxacin, 400 mg IV every 24 hours...
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unknown
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Femme et Homme Max 99 ans
Bayer HealthCare AG, Bayer Vital GmbH, D-51368 Leverkusen
MAJ Il y a 4 ans
Estudio de extensión a largo plazo, multicéntrico y multinacional, para evaluar la seguridad y tolerabilidad de BAY 63 2521 (1 mg, 1,5 mg, 2 mg o 2,5 mg tid) administrado por vía oral, en pacientes con Hipertensión Pulmonar Tromboembólica Crónica (HPTEC) Estudio CHEST-2
Long-term safety and tolerability of BAY 63-2521 in patients with inoperable Chronic Thromboembolic Pulmonary Hypertension (CTEPH) or recurrent or persisting pulmonary hypertension after surgical trea...
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Essai clos aux inclusions
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Homme Max 99 ans
Bayer HealthCare AG
MAJ Il y a 4 ans
A Phase 2/ 3 trial to evaluate the efficacy and safety of BAY86-6150 Studio di Fase II/III per valutare la sicurezza e l’efficacia di BAY 86-6150
Part A: - To identify the recommended dose by conducting a risk-benefit assessment of four different dose levels of BAY 86-6150 based on safety and dose response assessments in acutely bleeding subje...
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Femme et Homme Max 99 ans
Bayer HealthCare AG
MAJ Il y a 4 ans
RECORD 1 Study: REgulation of Coaculation in ORthopedic Surgery to prevent DVT and PE, controlled, double-blind, randomized study of BAY 59-7939 in the extended prevention of VTE in patients undergoing elective total hip replacement
The objective of this trial is to assess the efficacy and safety of BAY 59-7939 10 mg once daily dosing in extended prevention of VTE in men and women aged 18 years or above undergoing elective total ...
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unknown
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Homme Max 99 ans
Bayer HealthCare AG
MAJ Il y a 4 ans
Randomized, active-controlled, double-blind, parallel design study to evaluate the efficacy and safety of a once-a-week prophylaxis treatment with BAY 79-4980 compared to three times-per-week prophylaxis with rFVIII-FS in previously treated patients with severe hemophilia A
The primary objective is to evaluate the effect of a once-a-week prophylaxis regimen with BAY 79-4980 on the protection from total bleeds compared to a three times-per-week prophylaxis regimen with rF...
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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 4 ans
RECORD 2 Study: REgulation of Coagulation in ORthopedic Surgery to prevent DVT and PE, controlled, Double-Blind, Randomized Study of BAY59-7939 in the Extended Prevention of VTE in Patients Undergoing Elective Total Hip Replacement
The objective of this trial is to compare the efficacy and safety of VTE prophylaxis with BAY 59-7939 10 mg once daily administered for 5 weeks to enoxaparin 40 mg once daily (qd) administered for 10-...
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