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Daiichi Sankyo/AstraZeneca (AZN.US) received approval in China for the fourth indication of Durvalumab.
Recently, the fourth indication for which the combination development and commercialization of the dequ medical vumab monoclonal antibody developed jointly by Astrazeneca (AZN.US) and Daiichi Sankyo has been approved in China is for the treatment of adults with unresectable or metastatic non-small cell lung cancer with HER2 (ERBB2) activating mutations who have received at least one prior systemic therapy.
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