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    [{"orgOrder":0,"company":"Kato Pharmaceuticals","sponsor":"Not Applicable","pharmaFlowCategory":"DU","amount":"Not Applicable","upfrontCash":"Not Applicable","newsHeadline":"Kato Wins FDA Approval for Human Studies of Drug for Retinal Disorders","therapeuticArea":"Ophthalmology","highestDevelopmentStatus":"IND Enabling","country":"U.S.A","productType":"Small molecule","productStatus":"New Molecular Entity","date":"February 2022","url1":"","url2":"","graph1":"Ophthalmology","graph2":"IND Enabling"}]

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              Kato Wins FDA Approval for Human Studies of Drug for Retinal Disorders

              Details:

              The approval allows Kato to study the efficacy of Resolv ER, first-in-class patented formulation therapeutic drug is intended to separate the vitreous from the retina on VMA which may lead to retinal tears, retinal detachment, and macular holes.

              Lead Product(s): Liposome-loaded urea compound

              Therapeutic Area: Ophthalmology Product Name: Resolv ER

              Highest Development Status: IND Enabling Product Type: Small molecule

              Partner/Sponsor/Collaborator: Not Applicable

              Deal Size: Not Applicable Upfront Cash: Not Applicable

              Deal Type: Not Applicable February 16, 2022

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