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Kusajili – Clinical trials directory
Result
of your search per sponsor: Bayer HealthCare AG
Woman and Man Max 99 years
Bayer HealthCare AG
Update Il y a 4 ans
Rivaroxaban for the prevention of major cardiovascular events in coronary or peripheral artery disease
Primary objectives for rivaroxaban randomization: •To determine whether rivaroxaban 2.5 mg twice daily (bid) + aspirin 100 mg once daily (od) compared with aspirin 100 mg od reduces the risk of a com...
Country
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organs
None
Specialty
None
unknown
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Woman and Man Max 99 years
Bayer HealthCare AG
Update Il y a 4 ans
A multi-center, randomized, double blind, placebo controlled study to investigate the efficacy and safety of Aprotinin on transfusion requirements in patients with bladder cancer undergoing radical or total cystectomy
Main objective: The objective of this study is to evaluate the safety and efficacy of aprotinin as compared to placebo, in reducing the need for subsequent blood transfusion in subjects with bladder c...
Country
None
organs
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Specialty
None
Closed trial
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Woman and Man Max 99 years
Bayer HealthCare AG
Update Il y a 4 ans
Study to research BAY 1021189 in patients with worsening heart failure with preserved ejection fraction
To find the optimal dose of BAY 1021189 for Phase III that can be given in addition to standard diuretic and comorbidity treatment by characterizing the safety, tolerability, pharmacodynamic effects, ...
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
Bayer HealthCare AG
Update Il y a 4 ans
Randomized, double-blind, placebo-controlled, multicenter study to evaluate the safety and efficacy of inhaled ciprofloxacin compared to placebo in subjects with cystic fibrosis
The primary objective is to compare the change in FEV1 from baseline to Day 28-30 between Cipro Inhale-treated and placebo-treated subjects after a 4-week treatment period
Country
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organs
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Specialty
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Closed trial
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Woman and Man Max 99 years
Bayer HealthCare AG, D-51368 Leverkusen
Update Il y a 4 ans
Randomized, double-blind, placebo-controlled, multi-centre, multi-national study to evaluate the efficacy and safety of oral BAY 63-2521 (1 mg, 1.5 mg, 2 mg, or 2.5 mg tid) in patients with symptomatic Pulmonary Arterial Hypertension (PAH)
To assess the efficacy and safety of oral BAY 63-2521 (1 mg, 1.5 mg, 2 mg, or 2.5 mg tid) in treatment naive patients and patients pretreated with an Endothelin Receptor Antagonist or a Prostacyclin a...
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
Bayer HealthCare AG
Update Il y a 4 ans
Ciprofloxacin dry powder for inhalation in non-cystic fibrosis bronchiectasis (non–CF BE) Ciprofloxacin dry powder for inhalation in non-cystic fibrosis bronchiectasis (non–CF BE)
The primary objectives of the study are: • To evaluate the efficacy of ciprofloxacin DPI administered BID intermittently for 28 days on study treatment / 28 days off study treatment or 14 days on stu...
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
Bayer HealthCare AG
Update Il y a 4 ans
Rivaroxaban for treatment of venous or arterial blood clots in children from birth to less than 6 months Rivaroxabán en neonatos hasta menos de 6 meses para el tratamiento de trombosis arterial o venosa
to characterize the pharmacokinetic/pharmacodynamic profile of a 7-day treatment with oral rivaroxaban caracterizar el perfil farmacocinético y farmacodinámico del tratamiento con rivaroxabán or...
Country
None
organs
None
Specialty
None
unknown
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Man Max 99 years
Bayer HealthCare AG
Update Il y a 4 ans
A phase II/III, randomized, cross-over, open-label trial to demonstrate superiority of prophylaxis over on-demand therapy in previously treated subjects with severe hemophilia A treated with plasma protein-free recombinant FVIII formulated with sucrose (BAY 81-8973)
To demonstrate the superiority of prophylaxis over on demand therapy by a clinically significant decrease in bleeding rate following 12 months of treatment with BAY 81-8973.
Country
None
organs
None
Specialty
None
Closed trial
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Woman Max 99 years
Bayer HealthCare AG
Update Il y a 4 ans
Multi-center, open-label, randomized, parallel-group comparison of cycle control, bleeding pattern, lipid and carbohydrate metabolism of the transdermal contraceptive patch containing 0.55 mg ethinylestradiol and 2.1 mg gestodene (material no. 80876395) in a 21-day regimen vs. a comparator patch EVRA® (0.6 mg ethinylestradiol and 6 mg norelgestromin) in a 21-day regimen for 7 cycles in 400 women
The primary objective is to investigate the bleeding pattern and cycle control parameters of the transdermal contraceptive patch FC Patch Low (material no. 80876395 containing 0.55 mg EE and 2.1 mg GS...
Country
None
organs
None
Specialty
None
Closed trial
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Woman and Man Max 99 years
Bayer HealthCare AG
Update Il y a 4 ans
A randomized, double-masked, sham-controlled phase 3b/4 study of the efficacy, safety, and tolerability of intravitreal aflibercept monotherapy compared to aflibercept with adjunctive photodynamic therapy as indicated in subjects with polypoidal choroidal vasculopathy (PLANET)
To collect data reflecting the efficacy and safety of aflibercept with and without photodynamic therapy rescue treatment in subjects diagnosed with the polypoidal choroidal vasculopathy subtype of wet...
Country
None
organs
None
Specialty
None
unknown
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