AstraZeneca's (AZN) Baxfendy, developed for the treatment of adults with insufficiently controlled hypertension, has been recommended for marketing authorization by the European Medicines Agency's Committee for Medicinal Products for Human Use, the agency said Friday.
The health agency said the recommendation is based on clinical trials showing statistically significant reductions in systolic and diastolic blood pressure compared with placebo in patients whose hypertension remained uncontrolled despite treatment with at least two medications.
The European Commission will make the final decision on marketing authorization, the agency said.
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