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    [{"orgOrder":0,"company":"Marizyme","sponsor":"Undisclosed","pharmaFlowCategory":"DU","therapeuticArea":"Cardiology\/Vascular Diseases","country":"U.S.A","productType":"Dietary Supplement","year":"2023","type":"Inapplicable","leadProduct":"Glutathione","moa":"||Glutathione reductase","graph1":"Cardiology\/Vascular Diseases","graph2":"Approved FDF","graph3":"Marizyme","amount2":0,"highestDevelopmentShortName":"Approved FDF","therapeuticAreaShortName":"Cardiovascular Diseases","amount2New":0,"dosageForm":"Solution","sponsorNew":"Marizyme \/ Undisclosed","highestDevelopmentStatusID":"15","companyTruncated":"Marizyme \/ Undisclosed"}]

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                            Lead Product(s) : Glutathione,Ascorbic Acid

                            Therapeutic Area : Cardiology/Vascular Diseases

                            Study Phase : Approved FDF

                            Sponsor : Undisclosed

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            Marizyme, Inc. Announces FDA Clearance for Flagship Product, DuraGraft™

                            Details : DuraGraft is a first-in-class CE marked intra-operative graft storage solution used during bypass surgeries that is authorized for use in Europe and other countries outside of the United States.

                            Product Name : DuraGraft

                            Product Type : Dietary Supplement

                            Upfront Cash : Inapplicable

                            October 06, 2023

                            Lead Product(s) : Glutathione,Ascorbic Acid

                            Therapeutic Area : Cardiology/Vascular Diseases

                            Highest Development Status : Approved FDF

                            Sponsor : Undisclosed

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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