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FDA Approves HETLIOZ for Nighttime Sleep Disturbances in Smith-Magenis Syndrome americanpharmaceuticalreview
December 22, 2020Vanda Pharmaceuticals announced the U.S. Food and Drug Administration (FDA) has approved HETLIOZ? (tasimelteon) capsule and liquid formulations for the treatment of adults and children, respectively, with nighttime sleep disturbances associated with ... -
Vanda Announces Positive Study Results for Hetlioz
americanpharmaceuticalreview
December 11, 2018Vanda announced Hetlioz (tasimelteon) improved sleep quality and increased sleep duration in patients with Smith-Magenis Syndrome (SMS) in a pivotal placebo controlled clinical study....
Pharma Sources Insight January 2025
