Search Results - "Strohmaier, Christine"
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A 24-Week, Randomized, Controlled Study to Evaluate the Tolerability, Safety and Efficacy of 2 Different Titration Schemes of the Rivastigmine Patch in Japanese Patients with Mild to Moderate Alzheimer's Disease
Published in Dementia and geriatric cognitive disorders extra (29-09-2015)“…Aim: To investigate whether 1-step titration of the rivastigmine patch (initiated at 5 cm 2 and titrated to 10 cm 2 after 4 weeks) is well tolerated in…”
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BGG 492 as an adjunctive treatment in patients with partial‐onset seizures: A 12‐week, randomized, double‐blind, placebo‐controlled, phase II dose‐titration study with an open‐label extension
Published in Epilepsia (Copenhagen) (01-07-2017)“…Summary Objectives To evaluate dose–response relationship of BGG 492 as add‐on therapy to 1–3 antiepileptic drugs in patients with partial‐onset seizures and…”
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BGG492 as an adjunctive treatment in patients with partial‐onset seizures: A 12‐week, randomized, double‐blind, placebo‐controlled, phase II dose‐titration study with an open‐label extension
Published in Epilepsia (Copenhagen) (01-07-2017)“…Summary Objectives To evaluate dose–response relationship of BGG492 as add‐on therapy to 1–3 antiepileptic drugs in patients with partial‐onset seizures and to…”
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Randomized, double-blind, parallel-group, 48-week study for efficacy and safety of a higher-dose rivastigmine patch (15 vs. 10 cm²) in Alzheimer's disease
Published in Dementia and geriatric cognitive disorders (01-07-2012)“…Determine whether patients with Alzheimer's disease demonstrating functional and cognitive decline, following 24-48 weeks of open-label treatment with 9.5…”
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Long-term safety of rivastigmine in parkinson disease dementia: an open-label, randomized study
Published in Clinical neuropharmacology (01-01-2014)“…This study investigated the long-term safety of rivastigmine (12 mg/d capsules, 9.5 mg/24 h patch) and effects on motor symptoms in patients with…”
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P4‐185: UP‐TITRATION TO HIGH‐DOSE 13.3 MG/24 H RIVASTIGMINE TRANSDERMAL PATCH MAY PROVIDE GREATER BENEFIT TO ALZHEIMER'S DISEASE PATIENTS COMPARED TO CONCOMITANT USE OF 9.5 MG/24 H PATCH AND MEMANTINE: RESULTS FROM THE OPTIMA STUDY
Published in Alzheimer's & dementia (01-07-2014)Get full text
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Rivastigmine Patch in Chinese Patients with Probable Alzheimer's disease: A 24‐week, Randomized, Double‐Blind Parallel‐Group Study Comparing Rivastigmine Patch (9.5 mg/24 h) with Capsule (6 mg Twice Daily)
Published in CNS neuroscience & therapeutics (01-06-2016)“…Summary Aims To compare the once‐daily rivastigmine patch 9.5 mg/24 h (10 cm2) versus twice‐daily capsule (12 mg/day) in Chinese patients with probable…”
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UP-TITRATION TO HIGH-DOSE 13.3 MG/24 H RIVASTIGMINE TRANSDERMAL PATCH MAY PROVIDE GREATER BENEFIT TO ALZHEIMER'S DISEASE PATIENTS COMPARED TO CONCOMITANT USE OF 9.5 MG/24 H PATCH AND MEMANTINE: RESULTS FROM THE OPTIMA STUDY
Published in Alzheimer's & dementia (01-07-2014)Get full text
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P3–278: The rivastigmine high‐dose, 13 mg/24h (15cm2), transdermal patch provides daily living benefits to people with severe Alzheimer's disease: Retrospective analyses of the OPtimising Transdermal Exelon In Mild‐to‐moderate Alzheimer's disease (OPTIMA) study
Published in Alzheimer's & dementia (01-07-2013)Get full text
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The rivastigmine high-dose, 13 mg/24h (15cm2), transdermal patch provides daily living benefits to people with severe Alzheimer's disease: Retrospective analyses of the OPtimising Transdermal Exelon In Mild-to-moderate Alzheimer's disease (OPTIMA) study
Published in Alzheimer's & dementia (01-07-2013)Get full text
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Efficacy of Higher Dose 13.3 mg/24 h Rivastigmine Patch on Instrumental Activities of Daily Living in Patients with Mild-to-Moderate Alzheimer's Disease
Published in American journal of Alzheimer's disease and other dementias (01-09-2013)“…Background: Stabilizing/reducing decline in the ability to perform activities of daily living (ADLs) is important in management of Alzheimer’s disease (AD)…”
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Efficacy of the 13.3 mg/24 h rivastigmine patch on instrumental activities of daily living in the OPtimising Transdermal Exelon In Mild-to-moderate Alzheimer's disease (OPTIMA) study: Prospective subgroup analysis by disease severity and time-to-meet decline
Published in Alzheimer's & dementia (01-07-2012)Get full text
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