Takeda has requested a re-examination of its European application for melatonin agonist ramelteoon. In May the CHMP recommended that the EU not approve ramelteon due to questions on its efficacy in the treatment of insomnia.
Filed under: gpcr | Tagged: Melatonin, MT1, MT2, ramelteon, regulatory, Rozerem, TAK-375, TAK375, Takeda
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