生物技术公司Longeveron Inc宣布，美国食品药品监督管理局（FDA）已批准其召开C类会议的请求。此次会议旨在为其针对左心发育不全综合征（HLHS）疗法的关键性二期临床试验（Elpis II）的数据解读进行预备讨论。该试验的数据结果即将公布。
生物技术公司Longeveron Inc宣布，美国食品药品监督管理局（FDA）已批准其召开C类会议的请求。此次会议旨在为其针对左心发育不全综合征（HLHS）疗法的关键性二期临床试验（Elpis II）的数据解读进行预备讨论。该试验的数据结果即将公布。
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