新华制药：LXH-2103注射液获临床试验批准

南方财经网06-22

　　南财智讯6月22日电，新华制药公告，LXH-2103注射液收到国家药品监督管理局签发的《药物临床试验批准通知书》（通知书编号：2026LP01818），同意开展术后中至重度疼痛的临床试验。该药品为化学药品1类创新药，剂型为注射液，规格为1ml：50mg，拟用于术后中至重度疼痛治疗。

（文章来源：南方财经网）

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