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    [{"orgOrder":0,"company":"MavriX Bio","sponsor":"Inapplicable","pharmaFlowCategory":"DU","therapeuticArea":"Rare Diseases and Disorders","country":"U.S.A","productType":"Cell and Gene therapy","year":"2025","type":"Inapplicable","leadProduct":"MVX-220","moa":"UBE3A gene","graph1":"Rare Diseases and Disorders","graph2":"IND Enabling","graph3":"MavriX Bio","amount2":0,"highestDevelopmentShortName":"IND","therapeuticAreaShortName":"Rare Diseases","amount2New":0,"dosageForm":"Intra-cisterna magna Injection","sponsorNew":"MavriX Bio \/ Inapplicable","highestDevelopmentStatusID":"5","companyTruncated":"MavriX Bio \/ Inapplicable"}]

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                            Lead Product(s) : MVX-220

                            Therapeutic Area : Rare Diseases and Disorders

                            Study Phase : IND Enabling

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            MavriX Wins IND Clearance for Gene Therapy in Angelman Syndrome Trial

                            Details : MVX-220 is an investigational hu68AAV gene therapy designed to deliver the human UBE3A gene to neurons of the brain with a single intra-cisterna magna (ICM) injection.

                            Product Name : MVX-220

                            Product Type : Cell and Gene therapy

                            Upfront Cash : Inapplicable

                            May 12, 2025

                            Lead Product(s) : MVX-220

                            Therapeutic Area : Rare Diseases and Disorders

                            Highest Development Status : IND Enabling

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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