曼恩凯德生物医疗宣布，美国食品药品监督管理局（FDA）已接受审查该公司提交的补充生物制品许可申请（sBLA），该申请涉及其吸入胰岛素产品Afrezza在4-17岁糖尿病儿童和青少年患者中的应用。
曼恩凯德生物医疗宣布，美国食品药品监督管理局（FDA）已接受审查该公司提交的补充生物制品许可申请（sBLA），该申请涉及其吸入胰岛素产品Afrezza在4-17岁糖尿病儿童和青少年患者中的应用。
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