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项与 MSC Secretome Eye Drops(University of Illinois) 相关的临床试验Phase II Study of the Efficacy of Topical Mesenchymal Stromal Cell Secretome for Ocular Surface Disease
In this phase II randomized double-masked clinical trials, subjects with non-resolving corneal epithelial disease/defect (i.e., refractory to standard treatments for at least two weeks) will receive 8 weeks treatment of topical mesenchymal stem cell secretome or vehicle, with continued follow-up for up to Day 70.
Safety of Topical Mesenchymal Stromal Cell Secretome for Ocular Surface Disease
This study is a longitudinal assessment using a classic dose-escalation study design to assess the safety and maximal tolerated dose (MTD) of topical MSC Secretome eye drops. The study will be conducted at Illinois Eye and Ear Infirmary located at University of Illinois at Chicago. The study will use anterior segment Optical Coherence Tomography (OCT)/Scheimpflug Imaging, esthesiometry, and visual analogue scale (VAS) to assess treatment tolerability.
100 项与 MSC Secretome Eye Drops(University of Illinois) 相关的临床结果
100 项与 MSC Secretome Eye Drops(University of Illinois) 相关的转化医学
100 项与 MSC Secretome Eye Drops(University of Illinois) 相关的专利(医药)
100 项与 MSC Secretome Eye Drops(University of Illinois) 相关的药物交易