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【Portfolio】维眸生物招募首位受试者入组VVN001中国II期临床试验

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​​文章来源:维眸生物 http://www.vivavisionbio.com/

2021年12月10日

本临床研究由复旦大学附属耳鼻喉科医院徐建江教授牵头,后续将在全国多家医院迅速开展该项临床研究。本研究是一项评价VVN001滴眼液在中国干眼受试者中安全性和有效性的随机、双盲、溶媒对照、多中心的II期临床试验。

此前,VVN001滴眼液已顺利完成在健康成年受试者中的药代动力学和安全性的I期临床试验。在该研究中,未发生与药物相关的安全性事件,初步显示VVN001滴眼液的安全性良好。VVN001滴眼液对干眼患者的安全性和疗效将在II期临床试验中进一步研究,并在后续的研究过程对安全性进行持续的评估。

 

 

VVN001 滴眼液在美国开展的II期临床研究仍在顺利进行中。

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