[{"orgOrder":0,"company":"QBiotics Group","sponsor":"Inapplicable","pharmaFlowCategory":"DU","therapeuticArea":"Oncology","country":"AUSTRALIA","productType":"Other Small Molecule","year":"2021","type":"Inapplicable","leadProduct":"Tigilanol Tiglate","moa":"||Undisclosed","graph1":"Oncology","graph2":"Phase I\/ Phase II","graph3":"QBiotics Group","amount2":0,"highestDevelopmentShortName":"Ph I\/II","therapeuticAreaShortName":"Oncology","amount2New":0,"dosageForm":"Intravenous Injection","sponsorNew":"QBiotics Group \/ Inapplicable","highestDevelopmentStatusID":"7","companyTruncated":"QBiotics Group \/ Inapplicable"}]

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                          AACR Annual meeting
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                          AACR Annual meeting
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                          Details : The study will evaluate the safety, optimal dose and tumour response of the tigilanol tiglate and pembrolizumab combination in patients with late-stage unresectable melanoma, who have been previously exposed to immune checkpoint inhibitors.

                          Product Name : EBC-46

                          Product Type : Other Small Molecule

                          Upfront Cash : Inapplicable

                          February 06, 2021

                          Lead Product(s) : Tigilanol Tiglate,Pembrolizumab

                          Therapeutic Area : Oncology

                          Highest Development Status : Phase I/ Phase II

                          Sponsor : Inapplicable

                          Deal Size : Inapplicable

                          Deal Type : Inapplicable

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