悦康藥業(688658.SH):YKYY017霧化吸入劑獲得FDA臨牀試驗批准
格隆匯5月11日丨悦康藥業(688658.SH)公佈,公司於近日獲得美國食品藥品監督管理局關於同意YKYY017霧化吸入劑用於預防和治療新型冠狀病毒感染進行臨牀試驗的函(Study May
Proceed Letter,受理號:164988)。
YKYY017霧化吸入劑是公司與中國醫學科學院病原生物學研究所合作開發的最新一代廣譜、高效的冠狀病毒膜融合抑制劑,公司擁有YKYY017全球獨佔權益。
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