EU Grants Marketing Authorisation for Takeda’s Essential Hypertension Treatment
Takeda will launch azilsartan medoxomil across Europe in 2012 starting with Germany in January.
Takeda Pharmaceutical announced that the European Commission has granted marketing authorisation for Edarbi (azilsartan medoxomil), a new once-daily angiotensin receptor blocker (ARB) for the treatment of essential hypertension (high blood pressure) in adults.
Takeda will launch azilsartan medoxomil across Europe in 2012 starting with Germany in January.
The marketing authorisation follows a positive opinion from the Committee for Human Medicinal Products (CHMP) based on the results from an extensive pre-clinical and clinical development programme, including seven phase III clinical trials involving nearly 6,000 patients with essential hypertension.
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