An integrated review to evaluate dose response of umeclidinium (GSK573719) administered once or twice daily in Subjects with COPD The purpose of this study was to assess the total daily dose response of umeclidinium using pooled data from study AC4113073 and AC4115321 (excluding the site with Investigator ID of 040688) following...

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An open-label multicentre, randomised, phase II comparator study of oral topotecan versus intravenous topotecan for second-line therapy in sensitive patients with small cell lung cancer

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PRJ2203: A Prospective Observational Cohort Study to Monitor Occurrence of Hypersensitivity Reaction and Hepatotoxicity in Patients Receiving Dolutegravir Dolutegravir (DTG) is recommended for both treatment-naïve and treatment-experienced, HIV infected adults and paediatric patients aged 12 years and older and weighing at least 40 kg. One case of suspe...

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A multicentre, double-blind, parallel group, randomised dose study comparing the efficacy of paroxetine 20mg increasing to 30mg daily if there is insufficient response and clomipramine 60mg increasing to 75mg daily, in outpatients (age >60 years) with moderate depression according to…

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A Long-Term Extension of a Double-Blind, Placebo -Controlled Comparative Study of Paroxetine and Clomipramine in the Treatment of Panic Disorder

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Waterpipe use in the Middle East and North Africa: analysis of the BREATHE study

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A Phase I Study to Determine the Maximum Tolerated Dose of Topotecan Following Oral Administration over 5, 10 or 21 Days in Patients with Malignant Solid Tumors

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The long-term use of Advair/Seretide and risk of events (incident non-vertebral fracture, glaucoma, and cataracts) among COPD patients in the UK General Research Practice Database

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An investigation of the pharmacokinetics, efficacy, and tolerance of paroxetine in geriatric patients with depression

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A double-blind, placebo-controlled multi-centre study to evaluate the efficacy and tolerability of Paroxetine in the treatment of post-stroke depression

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