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    [{"orgOrder":0,"company":"Henlius","sponsor":"Inapplicable","pharmaFlowCategory":"DU","therapeuticArea":"Oncology","country":"CHINA","productType":"Antibody","year":"2023","type":"Inapplicable","leadProduct":"Carboplatin","moa":"||Programmed cell death protein 1","graph1":"Oncology","graph2":"Approved FDF","graph3":"Henlius","amount2":0,"highestDevelopmentShortName":"Approved FDF","therapeuticAreaShortName":"Oncology","amount2New":0,"dosageForm":"Intravenous Injection","sponsorNew":"Henlius \/ Inapplicable","highestDevelopmentStatusID":"15","companyTruncated":"Henlius \/ Inapplicable"},{"orgOrder":0,"company":"Henlius","sponsor":"Intas Pharmaceuticals","pharmaFlowCategory":"D","therapeuticArea":"Oncology","country":"CHINA","productType":"Antibody","year":"2023","type":"Collaboration","leadProduct":"5 Fluorouracil","moa":"||Programmed cell death protein 1","graph1":"Oncology","graph2":"Approved FDF","graph3":"Henlius","amount2":0.20000000000000001,"highestDevelopmentShortName":"Approved FDF","therapeuticAreaShortName":"Oncology","amount2New":0.20000000000000001,"dosageForm":"Intravenous Injection","sponsorNew":"Henlius \/ Intas Pharmaceuticals","highestDevelopmentStatusID":"15","companyTruncated":"Henlius \/ Intas Pharmaceuticals"},{"orgOrder":0,"company":"Henlius","sponsor":"Intas Pharmaceuticals","pharmaFlowCategory":"DU","therapeuticArea":"Oncology","country":"CHINA","productType":"Antibody","year":"2024","type":"Inapplicable","leadProduct":"Serplulimab","moa":"Programmed cell death protein 1","graph1":"Oncology","graph2":"Approved FDF","graph3":"Henlius","amount2":0,"highestDevelopmentShortName":"Approved FDF","therapeuticAreaShortName":"Oncology","amount2New":0,"dosageForm":"Intravenous Injection","sponsorNew":"Henlius \/ Intas Pharmaceuticals","highestDevelopmentStatusID":"15","companyTruncated":"Henlius \/ Intas Pharmaceuticals"},{"orgOrder":0,"company":"Henlius","sponsor":"Inapplicable","pharmaFlowCategory":"DU","therapeuticArea":"Oncology","country":"CHINA","productType":"Antibody","year":"2022","type":"Inapplicable","leadProduct":"Carboplatin","moa":"||Programmed cell death protein 1","graph1":"Oncology","graph2":"Approved FDF","graph3":"Henlius","amount2":0,"highestDevelopmentShortName":"Approved FDF","therapeuticAreaShortName":"Oncology","amount2New":0,"dosageForm":"Intravenous Injection","sponsorNew":"Henlius \/ Inapplicable","highestDevelopmentStatusID":"15","companyTruncated":"Henlius \/ Inapplicable"},{"orgOrder":0,"company":"Henlius","sponsor":"Inapplicable","pharmaFlowCategory":"DU","therapeuticArea":"Oncology","country":"CHINA","productType":"Antibody","year":"2021","type":"Inapplicable","leadProduct":"Serplulimab","moa":"Programmed cell death protein 1","graph1":"Oncology","graph2":"Phase III","graph3":"Henlius","amount2":0,"highestDevelopmentShortName":"Ph III","therapeuticAreaShortName":"Oncology","amount2New":0,"dosageForm":"Intravenous Injection","sponsorNew":"Henlius \/ Inapplicable","highestDevelopmentStatusID":"10","companyTruncated":"Henlius \/ Inapplicable"},{"orgOrder":0,"company":"Henlius","sponsor":"Inapplicable","pharmaFlowCategory":"DU","therapeuticArea":"Oncology","country":"CHINA","productType":"Antibody","year":"2022","type":"Inapplicable","leadProduct":"Bevacizumab","moa":"||Programmed cell death protein 1","graph1":"Oncology","graph2":"Phase II","graph3":"Henlius","amount2":0,"highestDevelopmentShortName":"Ph II","therapeuticAreaShortName":"Oncology","amount2New":0,"dosageForm":"Intravenous Injection","sponsorNew":"Henlius \/ Inapplicable","highestDevelopmentStatusID":"8","companyTruncated":"Henlius \/ Inapplicable"},{"orgOrder":0,"company":"Henlius","sponsor":"Palleon Pharmaceuticals","pharmaFlowCategory":"D","therapeuticArea":"Nephrology","country":"U.S.A","productType":"Enzyme","year":"2024","type":"Licensing Agreement","leadProduct":"Bi-Sialidase","moa":"||Glyco-immune checkpoint","graph1":"Nephrology","graph2":"Phase I\/ Phase II","graph3":"Henlius","amount2":0.10000000000000001,"highestDevelopmentShortName":"Ph I\/II","therapeuticAreaShortName":"Nephrology","amount2New":0.10000000000000001,"dosageForm":"Intravenous Infusion","sponsorNew":"Henlius \/ Henlius","highestDevelopmentStatusID":"7","companyTruncated":"Henlius \/ Henlius"},{"orgOrder":0,"company":"Henlius","sponsor":"Shanghai Henlius Biotech","pharmaFlowCategory":"DU","therapeuticArea":"Oncology","country":"CHINA","productType":"Antibody","year":"2024","type":"Inapplicable","leadProduct":"HLX22","moa":"HER2","graph1":"Oncology","graph2":"Phase III","graph3":"Henlius","amount2":0,"highestDevelopmentShortName":"Ph III","therapeuticAreaShortName":"Oncology","amount2New":0,"dosageForm":"Undisclosed","sponsorNew":"Henlius \/ Henlius","highestDevelopmentStatusID":"10","companyTruncated":"Henlius \/ Henlius"},{"orgOrder":0,"company":"Henlius","sponsor":"Essex Biotechnology","pharmaFlowCategory":"D","therapeuticArea":"Ophthalmology","country":"CHINA","productType":"Antibody","year":"2020","type":"Licensing Agreement","leadProduct":"Bevacizumab","moa":"Vascular endothelial growth factor A","graph1":"Ophthalmology","graph2":"Phase III","graph3":"Henlius","amount2":0.029999999999999999,"highestDevelopmentShortName":"Ph III","therapeuticAreaShortName":"Ophthalmology","amount2New":0.029999999999999999,"dosageForm":"Injection","sponsorNew":"Henlius \/ Henlius","highestDevelopmentStatusID":"10","companyTruncated":"Henlius \/ Henlius"},{"orgOrder":0,"company":"Henlius","sponsor":"Shanghai Henlius Biotech","pharmaFlowCategory":"DU","therapeuticArea":"Oncology","country":"CHINA","productType":"Undisclosed","year":"2025","type":"Inapplicable","leadProduct":"HLX43","moa":"Claudin 18.2","graph1":"Oncology","graph2":"Phase II","graph3":"Henlius","amount2":0,"highestDevelopmentShortName":"Ph II","therapeuticAreaShortName":"Oncology","amount2New":0,"dosageForm":"Undisclosed","sponsorNew":"Henlius \/ Henlius","highestDevelopmentStatusID":"8","companyTruncated":"Henlius \/ Henlius"},{"orgOrder":0,"company":"Henlius","sponsor":"Chiome Bioscience","pharmaFlowCategory":"D","therapeuticArea":"Oncology","country":"JAPAN","productType":"Antibody","year":"2021","type":"Licensing Agreement","leadProduct":"LIV-2008","moa":"Trop2","graph1":"Oncology","graph2":"Preclinical","graph3":"Henlius","amount2":0,"highestDevelopmentShortName":"Preclinical","therapeuticAreaShortName":"Oncology","amount2New":0,"dosageForm":"Undisclosed","sponsorNew":"Henlius \/ Henlius","highestDevelopmentStatusID":"4","companyTruncated":"Henlius \/ Henlius"}]

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                            01

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                            Lead Product(s) : HLX43

                            Therapeutic Area : Oncology

                            Study Phase : Phase II

                            Recipient : Shanghai Henlius Biotech

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

                            DEALS_DEV arrow-down

                            A Phase II Clinical Study to Evaluate HLX43 in Subjects With Advanced Non-small Cell Lung Cancer (NSCLC)

                            Details : Undisclosed

                            Product Name : Undisclosed

                            Product Type : Undisclosed

                            Upfront Cash : Inapplicable

                            April 02, 2025

                            Lead Product(s) : HLX43

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase II

                            Recipient : Shanghai Henlius Biotech

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            02

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                            Lead Product(s) : Bi-Sialidase,Rituximab

                            Therapeutic Area : Nephrology

                            Study Phase : Preclinical

                            Recipient : Palleon Pharmaceuticals

                            Deal Size : $95.3 million

                            Deal Type : Licensing Agreement

                            DEALS_DEV arrow-down

                            Palleon and Henlius Partner On Glycan Editing for Autoimmune Disease Treatment

                            Details : Henlius has obtained an exclusive license in China for E-602 and will advance its development in combination with Hanlikang for the treatment of autoimmune diseases, including lupus nephritis.

                            Product Name : Undisclosed

                            Product Type : Enzyme

                            Upfront Cash : Undisclosed

                            December 19, 2024

                            Lead Product(s) : Bi-Sialidase,Rituximab

                            Therapeutic Area : Nephrology

                            Highest Development Status : Preclinical

                            Recipient : Palleon Pharmaceuticals

                            Deal Size : $95.3 million

                            Deal Type : Licensing Agreement

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                            03

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                            Lead Product(s) : Serplulimab

                            Therapeutic Area : Oncology

                            Study Phase : Phase III

                            Sponsor : Intas Pharmaceuticals

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

                            DEALS_DEV arrow-down

                            Henlius, Intas Get CHMP Nod for HETRONIFLY® in Small Cell Lung Cancer

                            Details : Hetronifly (serplulimab) is a PD-1 inhibitor antibody, which is currently being evaluated for the treatment of patients with locally advanced or metastatic non-squamous non-small cell lung cancer.

                            Product Name : Hansizhuang

                            Product Type : Antibody

                            Upfront Cash : Inapplicable

                            September 21, 2024

                            Lead Product(s) : Serplulimab

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase III

                            Sponsor : Intas Pharmaceuticals

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            04

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                            Lead Product(s) : HLX22

                            Therapeutic Area : Oncology

                            Study Phase : Phase III

                            Recipient : Shanghai Henlius Biotech

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

                            DEALS_DEV arrow-down

                            A Phase â…¢ Clinical Study of HLX22 in Combination With Trastuzumab and Chemotherapy for the Treatment of ...

                            Details : Undisclosed

                            Product Name : Undisclosed

                            Product Type : Antibody

                            Upfront Cash : Inapplicable

                            August 01, 2024

                            Lead Product(s) : HLX22

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase III

                            Recipient : Shanghai Henlius Biotech

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            05

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                            Lead Product(s) : Serplulimab,Fluorouracil

                            Therapeutic Area : Oncology

                            Study Phase : Approved FDF

                            Sponsor : Intas Pharmaceuticals

                            Deal Size : $195.5 million

                            Deal Type : Collaboration

                            DEALS_DEV arrow-down

                            Henlius Deepens Collaboration with Intas to Bring Henlius' Novel anti-PD-1 mAb Serplulimab to Europe and India

                            Details : Under the terms of the agreement, Henlius will be responsible for clinical development, manufacturing and supply upon launch of specific formulation of HANSIZHUANG (serplulimab injection), Henlius' novel anti-PD-1 mAb.

                            Product Name : Hansizhuang

                            Product Type : Antibody

                            Upfront Cash : $44.4 million

                            October 27, 2023

                            Lead Product(s) : Serplulimab,Fluorouracil

                            Therapeutic Area : Oncology

                            Highest Development Status : Approved FDF

                            Sponsor : Intas Pharmaceuticals

                            Deal Size : $195.5 million

                            Deal Type : Collaboration

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                            06

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                            Lead Product(s) : Serplulimab,Carboplatin,Etoposide

                            Therapeutic Area : Oncology

                            Study Phase : Approved FDF

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

                            DEALS_DEV arrow-down

                            Henlius' Novel Anti-PD-1 mAb HANSIZHUANG (Serplulimab) Approved for the Treatment of ES-SCLC

                            Details : Hansizhuang (serplulimab) is a novel humanized monoclonal anti-PD-1 antibody, which is approved for the first-line treatment of extensive stage small cell lung cancer in combination with carboplatin and etoposide.

                            Product Name : Hansizhuang

                            Product Type : Antibody

                            Upfront Cash : Inapplicable

                            January 17, 2023

                            Lead Product(s) : Serplulimab,Carboplatin,Etoposide

                            Therapeutic Area : Oncology

                            Highest Development Status : Approved FDF

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            07

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                            Lead Product(s) : Serplulimab,Bevacizumab

                            Therapeutic Area : Oncology

                            Study Phase : Phase II

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

                            DEALS_DEV arrow-down

                            Phase 2 Study of the PD-1 Inhibitor Serplulimab Plus the Bevacizumab Biosimilar HANBEITAI in Patients with Adv...

                            Details : Results from both groups (group A, n=20; group B, n=21) demonstrated that Hansizhuang (serplulimab) plus HLX04 was safe and well-tolerated. As assessed by IRRC, the ORR was 30.0% (95% CI, 11.9–54.3) in group A and 14.3% (95% CI, 3.0–36.3) in group B.

                            Product Name : Hansizhuang

                            Product Type : Antibody

                            Upfront Cash : Inapplicable

                            September 09, 2022

                            Lead Product(s) : Serplulimab,Bevacizumab

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase II

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            08

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                            Lead Product(s) : Serplulimab,Carboplatin

                            Therapeutic Area : Oncology

                            Study Phase : Phase III

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

                            DEALS_DEV arrow-down

                            ASTRUM-005: Henlius Released Phase 3 Study Results for the First-line Treatment of Small Cell Lung Cancer of S...

                            Details : The study results demonstrated that HLX10 (serplulimab) in combination with chemotherapy can significantly extend median OS to 15.4 months when compared to control group in first-line SCLC, gaining global recognition while leapfrogging immunotherapy trea...

                            Product Name : Hansizhuang

                            Product Type : Antibody

                            Upfront Cash : Inapplicable

                            June 06, 2022

                            Lead Product(s) : Serplulimab,Carboplatin

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase III

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            09

                            Henlius

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                            Lead Product(s) : Serplulimab

                            Therapeutic Area : Oncology

                            Study Phase : Phase III

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

                            DEALS_DEV arrow-down

                            Henlius will Release 4 Oral Presentations of 2 Upcoming Commercial Products: Novel anti-PD-1 mAb Serplulimab a...

                            Details : Henlius will release 4 study results of 2 products to be commercialized, the novel anti-PD-1 mAb serplulimab and the bevacizumab biosimilar HLX04 used in patients with advanced hepatocellular carcinoma. Serplulimab injection is anti-PD-1 mAb for treatmen...

                            Product Name : Hansizhuang

                            Product Type : Antibody

                            Upfront Cash : Inapplicable

                            September 18, 2021

                            Lead Product(s) : Serplulimab

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase III

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            10

                            Henlius

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                            Lead Product(s) : LIV-2008

                            Therapeutic Area : Oncology

                            Study Phase : Preclinical

                            Recipient : Chiome Bioscience

                            Deal Size : Undisclosed

                            Deal Type : Licensing Agreement

                            DEALS_DEV arrow-down

                            Henlius Has Reached an Exclusive License Agreement with Chiome for Antibodies Targeting Human TROP2

                            Details : Chiome agreed to grant Henlius an exclusive right and license to antibodies targeting human TROP2 and related intellectual property rights to research, develop, manufacture and commercialize the Licensed Products in China.

                            Product Name : Undisclosed

                            Product Type : Antibody

                            Upfront Cash : Undisclosed

                            January 14, 2021

                            Lead Product(s) : LIV-2008

                            Therapeutic Area : Oncology

                            Highest Development Status : Preclinical

                            Recipient : Chiome Bioscience

                            Deal Size : Undisclosed

                            Deal Type : Licensing Agreement

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