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Takeda to appeal EU negative opinion on melatonin agonist ramelteon

Posted on June 17, 2008 by crimsoncanary

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

« Acadias ACP-104 does not meet endpoint in Phase IIb Schizophrenia trial Daiichi-Sankyos Angiotensin II 1 antagonist olmesartan reverses blood vessel damage »

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