[{"orgOrder":0,"company":"Tianjin Tasly Group","sponsor":"Sutro Biopharma","pharmaFlowCategory":"D","therapeuticArea":"Oncology","country":"U.S.A","productType":"Antibody-drug Conjugate","year":"2021","type":"Licensing Agreement","leadProduct":"Luveltamab Tazevibulin","moa":"Folate receptor alpha","graph1":"Oncology","graph2":"Phase II\/ Phase III","graph3":"Tianjin Tasly Group","amount2":0,"highestDevelopmentShortName":"Ph II\/III","therapeuticAreaShortName":"Oncology","amount2New":0,"dosageForm":"Intravenous Infusion","sponsorNew":"Tianjin Tasly Group \/ Tianjin Tasly Group","highestDevelopmentStatusID":"9","companyTruncated":"Tianjin Tasly Group \/ Tianjin Tasly Group"}]

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                          01

                          BioAsia
                          Not Confirmed
                          BioAsia
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                          Details : Under the terms of the agreement, Tasly will pursue the clinical development, regulatory approval, and commercialization of STRO-002 in Greater China for ovarian and endometrial cancers.

                          Product Name : STRO-002

                          Product Type : Antibody-drug Conjugate

                          Upfront Cash : $40.0 million

                          December 27, 2021

                          Lead Product(s) : Luveltamab Tazevibulin

                          Therapeutic Area : Oncology

                          Highest Development Status : Phase I

                          Recipient : Sutro Biopharma

                          Deal Size : $385.0 million

                          Deal Type : Licensing Agreement

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