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David A. Amato

Researcher at Sunovion

Publications -  12
Citations -  1575

David A. Amato is an academic researcher from Sunovion. The author has contributed to research in topics: Eszopiclone & Insomnia. The author has an hindex of 9, co-authored 12 publications receiving 1511 citations.

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Eszopiclone co-administered with fluoxetine in patients with insomnia coexisting with major depressive disorder.

TL;DR: Eszopiclone/fluoxetine co-therapy was relatively well tolerated and associated with rapid, substantial, and sustained sleep improvement, a faster onset of antidepressant response on the basis of CGI, and a greater magnitude of the antidepressant effect.
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Sustained efficacy of eszopiclone over 6 months of nightly treatment: results of a randomized, double-blind, placebo-controlled study in adults with chronic insomnia.

TL;DR: Throughout 6 months, eszopiclone improved all of the components of insomnia as defined by DSM-IV, including patient ratings of daytime function, which is compelling evidence that long-term pharmacologic treatment of insomnia is efficacious.
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Nightly Treatment of Primary Insomnia With Eszopiclone for Six Months: Effect on Sleep, Quality of Life, and Work Limitations

TL;DR: This is the first placebo-controlled investigation to demonstrate that long-term nightly pharmacologic treatment of primary insomnia with any hypnotic enhanced quality of life, reduced work limitations, and reduced global insomnia severity, in addition to improving patient-reported sleep variables.
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A 2-week efficacy and safety study of eszopiclone in elderly patients with primary insomnia.

TL;DR: Ezopiclone was well tolerated in elderly patients with primary insomnia, and the sleep efficacy was accompanied by significantly less napping and significantly higher ratings of daytime alertness, sense of physical well-being, and several quality-of-life parameters at the higher dose.
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Efficacy and safety of eszopiclone across 6-weeks of treatment for primary insomnia.

TL;DR: Patients treated with nightly eszopiclone 3 mg had better polysomnographic and patient-reported measures of sleep over the 6-week trial and no detrimental effects on next-day psychomotor performance using the DSST.