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AstraZeneca reports EMA validation of Type II Variation application for Enhertu

Daiichi Sankyo and AstraZeneca announced that the European Medicines Agency, or EMA, has validated the Type II Variation application for Enhertu as a monotherapy for the treatment of adult patients with unresectable or metastatic HER2 low or HER2 ultralow breast cancer who have received at least one endocrine therapy in the metastatic setting.

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