Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
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Sankyo Receives Approvable Letter for CS-866 from US FDA
Sankyo announced on October 29 that its 100%-owned US subsidiary Sankyo Pharma, Inc received an approvable letter for its antihypertensive agent CS-866 (olmesartan medoxomil) on October 24 from the US FDA. CS-866 is an angiotensin II receptor antagonist which Sankyo…
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