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    [{"orgOrder":0,"company":"CellTrans","sponsor":"Inapplicable","pharmaFlowCategory":"DU","therapeuticArea":"Endocrinology","country":"U.S.A","productType":"Cell and Gene therapy","year":"2023","type":"Inapplicable","leadProduct":"Donislecel","moa":"Undisclosed","graph1":"Endocrinology","graph2":"Approved FDF","graph3":"CellTrans","amount2":0,"highestDevelopmentShortName":"","therapeuticAreaShortName":"Endocrinology","amount2New":0,"dosageForm":"Intraportal Infusion","sponsorNew":"CellTrans \/ Inapplicable","highestDevelopmentStatusID":"15","companyTruncated":"CellTrans \/ Inapplicable"}]

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                            Lead Product(s) : Donislecel

                            Therapeutic Area : Endocrinology

                            Study Phase : Approved FDF

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            FDA Approves First Cellular Therapy to Treat Patients with Type 1 Diabetes

                            Details : Lantidra (donislecel-jujn suspension for hepatic portal vein infusion) is an allogeneic pancreatic islet cellular therapy y indicated for the treatment of adults with Type 1 diabetes who are unable to approach target HbA1c.

                            Product Name : Lantidra

                            Product Type : Cell and Gene therapy

                            Upfront Cash : Inapplicable

                            June 29, 2023

                            Lead Product(s) : Donislecel

                            Therapeutic Area : Endocrinology

                            Highest Development Status : Approved FDF

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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