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Kusajili – Centralise les essais cliniques mondiaux
Résultat
de votre recherche par promoteur : GlaxoSmithKline Research and Development Ltd
Femme et Homme Max 99 ans
GlaxoSmithKline Research and Development Ltd
MAJ Il y a 4 ans
A dose-ranging study of Vilanterol (VI) inhalation powder in children aged 5-11 years with asthma
The primary objective is to evaluate the dose response, efficacy and safety of three doses of VI inhalation powder administered once daily in the evening in children aged 5-11 years with persistent un...
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Essai clos aux inclusions
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Femme et Homme Max 99 ans
GlaxoSmithKline Research and Development Ltd
MAJ Il y a 4 ans
A Phase III Multicenter, Randomized, Double-Blind, Active-Controlled, Parallel Group Study of the Efficacy and Safety of the Intravenous and Oral Formulations of the Neurokinin-1 Receptor Antagonist, Casopitant, administered in Combination with ZOFRAN and Dexamethasone for Prevention of Chemotherapy-Induced Nausea and Vomiting in Cancer Subjects Receiving Highly Emetogenic Cisplatin-Based Chemotherapy
The primary objective of this study is to demonstrate the superiority of triple therapy, casopitant, ZOFRAN and dexamethasone over dual therapy ZOFRAN and dexamethasone in prevention of emesis over th...
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unknown
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Femme et Homme Max 99 ans
GlaxoSmithKline Research and Development Ltd
MAJ Il y a 4 ans
Study to assess the effect of fluticasone furoate on growth rate in children aged 5-11
To evaluate the effect of two weeks treatment with inhaled fluticasone furoate versus placebo once daily on short-term lower-leg growth using a knemometer.
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Essai clos aux inclusions
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Homme Max 99 ans
GlaxoSmithKline Research and Development Ltd
MAJ Il y a 4 ans
A Randomised, Double-Blind, Placebo-Controlled Trial Assessing the Efficacy and Safety of Dutasteride (AVODART™) 0.5 mg in Extending the Time to PSA Doubling in Men with Prostate Cancer and Biochemical Failure (PSA increase) after Radical Therapy with Curative Intent (ARTS – AVODART after Radical Therapy for prostate cancer Study)
To assess the effect of dutasteride 0.5 mg daily compared to placebo on time to PSA doubling
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Essai clos aux inclusions
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Femme et Homme Max 99 ans
GlaxoSmithKline Research and Development Ltd
MAJ Il y a 4 ans
A Randomized Double-Blind Placebo-Controlled, Parallel-Group, Multicenter, Study to Evaluate the Efficacy and Safety of GW685698X Inhalation Powder 25mcg, 50mcg, 100mcg, and 200mcg Administered Once Daily in the Morning and Fluticasone Propionate 100mcg BID via DISKUS Inhalation Powder compared with Placebo for 8 Weeks in Adolescent and Adult Subjects (≥12 years old) with Persistent Asthma Symptomatic on Non-ICS Therapy
The objective of this study is to evaluate the dose response of four dosage regimens of GW685698X (25mcg, 50mcg, 100mcg and 200mcg) administered once daily in the morning in adolescent and adult subje...
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Essai clos aux inclusions
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Femme et Homme Max 99 ans
GlaxoSmithKline Research and Development Ltd
MAJ Il y a 4 ans
A Phase IIb pilot study to assess the antiviral activity of GSK1349572 containing regimen in antiretroviral therapy (ART)-experienced, HIV-1-infected adult subjects with raltegravir resistance
To assess the short-term antiviral activity of GSK1349572 + failing background regimen.
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Essai clos aux inclusions
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Femme et Homme Max 99 ans
GlaxoSmithKline Research and Development Ltd
MAJ Il y a 4 ans
A MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL GROUP STUDY TO EVALUATE THE SAFETY AND EFFICACY OF LAMOTRIGINE 200-400MG/DAY COMPARED WITH PLACEBO IN SUBJECTS WITH PAINFUL DIABETIC NEUROPATHY
To evaluate the efficacy of lamotrigine (LTG) extended release compared with placebo for the treatment of pain associated with diabetic neuropathy.
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unknown
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Femme Max 99 ans
GlaxoSmithKline Research and Development Ltd
MAJ Il y a 4 ans
A randomized, double-blind, placebo-controlled, dose ranging study to investigate the safety, tolerability, pharmacokinetics and pharmacodynamics of GSK221149A administered intravenously in healthy, pregnant females, with uncomplicated preterm labor between 30 0/7 - 35 6/7 weeks gestation
1. To describe the maternal safety and tolerability of GSK221149A administered intravenously to healthy pregnant women in PTL between 30 0/7 and 35 6/7 weeks gestation 2. To describe the fetal safety ...
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Essai clos aux inclusions
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Femme et Homme Max 99 ans
GlaxoSmithKline Research and Development Ltd
MAJ Il y a 4 ans
A Randomized, Double-Blind, Placebo-Controlled Multicenter Phase II Study to Evaluate the Safety and Efficacy and Dose Response of 28 Days of Once-Daily Dosing of the Oral Motilin Receptor Agonist GSK962040, in Type I and II Diabetic Male and Female Subjects with Gastroparesis
To investigate the pharmacodynamic effect of 28 days of repeated doses of GSK962040 on gastric emptying of an isotope-labelled test meal, as measured by the 13C-oral breath test (OBT) in DM subjects w...
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unknown
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Femme et Homme Max 99 ans
GlaxoSmithKline Research and Development Ltd
MAJ Il y a 4 ans
A randomized, double blind, double dummy, parallel group, placebo controlled study to evaluate the pharmacodynamic and pharmacokinetic response and safety and tolerability of SB424323 (250 mg, 375 mg and 500 mg) administered twice daily for 16 weeks, on top of aspirin (325 mg, qd) in men and women with non valvular atrial fibrillation at a low or intermediate risk for stroke
To characterize the relationship between anti IIa activity, a biomarker used to detect changes in coagulability, and SB424323 dosage.
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Essai clos aux inclusions
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