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Applicable","highestDevelopmentStatusID":null,"companyTruncated":"Merck & Co.."},{"orgOrder":0,"company":"Ultimovacs","sponsor":"Not Applicable","pharmaFlowCategory":"DU","amount":"Not Applicable","upfrontCash":"Not Applicable","newsHeadline":"Ultimovacs Provide Update from Ph I Study Showing Strong Survival with UV1 & Pembrolizumab","therapeuticArea":"Oncology","highestDevelopmentStatus":"Phase I","country":"","productType":"Vaccine","productStatus":"New Molecular Entity","date":"June 2024","year":"2024","type":"Not Applicable","leadProduct":"Pembrolizumab","moa":"","url1":"","url2":"","graph1":null,"graph2":null,"graph3":"Ultimovacs","amount2":0,"therapeuticAreaNew":null,"highestDevelopmentStatusNew":null,"highestDevelopmentShortName":null,"therapeuticAreaShortName":null,"productSubType":"","amount2New":0,"dosageForm":"","sponsorNew":"Ultimovacs \/ Not Applicable","highestDevelopmentStatusID":null,"companyTruncated":"Ultimovacs.."},{"orgOrder":0,"company":"Merck & Co","sponsor":"Not Applicable","pharmaFlowCategory":"DU","amount":"Not Applicable","upfrontCash":"Not Applicable","newsHeadline":"FDA Grants Priority Review to Merck\u2019s KEYTRUDA Plus Chemotherapy for Advanced Mesothelioma","therapeuticArea":"Oncology","highestDevelopmentStatus":"Phase II\/ Phase III","country":"","productType":"Large molecule","productStatus":"Approved","date":"May 2024","year":"2024","type":"Not Applicable","leadProduct":"Pembrolizumab","moa":"","url1":"","url2":"","graph1":null,"graph2":null,"graph3":"Merck & Co","amount2":0,"therapeuticAreaNew":null,"highestDevelopmentStatusNew":null,"highestDevelopmentShortName":null,"therapeuticAreaShortName":null,"productSubType":"","amount2New":0,"dosageForm":"","sponsorNew":"Merck & Co \/ Not Applicable","highestDevelopmentStatusID":null,"companyTruncated":"Merck & Co.."},{"orgOrder":0,"company":"Kintara Therapeutics","sponsor":"TuHURA Biosciences","pharmaFlowCategory":"D","amount":"$5.0 million","upfrontCash":"Undisclosed","newsHeadline":"Kineta Signs Exclusivity Agreement for VISTA Blocking Antibody with TuHURA Biosciences","therapeuticArea":"Oncology","highestDevelopmentStatus":"Phase I\/ Phase II","country":"","productType":"Large molecule","productStatus":"New Molecular Entity","date":"July 2024","year":"2024","type":"Agreement","leadProduct":"KVA12123","moa":"","url1":"","url2":"","graph1":null,"graph2":null,"graph3":"Kintara Therapeutics","amount2":0.01,"therapeuticAreaNew":null,"highestDevelopmentStatusNew":null,"highestDevelopmentShortName":null,"therapeuticAreaShortName":null,"productSubType":"","amount2New":0,"dosageForm":"","sponsorNew":"Kintara Therapeutics \/ TuHURA Biosciences","highestDevelopmentStatusID":null,"companyTruncated":"Kintara Th.."},{"orgOrder":0,"company":"Sanofi","sponsor":"Vir Biotechnology","pharmaFlowCategory":"D","amount":"Undisclosed","upfrontCash":"Undisclosed","newsHeadline":"Vir Biotechnology Expands with Worldwide License Agreement with Sanofi for T-cell Engagers","therapeuticArea":"Oncology","highestDevelopmentStatus":"Phase I\/ Phase II","country":"","productType":"Cell and Gene therapy","productStatus":"New Molecular Entity","date":"August 2024","year":"2024","type":"Licensing Agreement","leadProduct":"AMX-818","moa":"","url1":"","url2":"","graph1":null,"graph2":null,"graph3":"Sanofi","amount2":0,"therapeuticAreaNew":null,"highestDevelopmentStatusNew":null,"highestDevelopmentShortName":null,"therapeuticAreaShortName":null,"productSubType":"","amount2New":0,"dosageForm":"","sponsorNew":"Sanofi \/ Vir Biotechnology","highestDevelopmentStatusID":null,"companyTruncated":"Sanofi \/ V.."},{"orgOrder":0,"company":"BioNTech","sponsor":"Genmab","pharmaFlowCategory":"D","amount":"Undisclosed","upfrontCash":"Undisclosed","newsHeadline":"Genmab Takes Full Control of Acasunlimab Development Program","therapeuticArea":"Oncology","highestDevelopmentStatus":"Phase II","country":"","productType":"Large molecule","productStatus":"New Molecular Entity","date":"August 2024","year":"2024","type":"Termination","leadProduct":"Acasunlimab","moa":"","url1":"","url2":"","graph1":null,"graph2":null,"graph3":"BioNTech","amount2":0,"therapeuticAreaNew":null,"highestDevelopmentStatusNew":null,"highestDevelopmentShortName":null,"therapeuticAreaShortName":null,"productSubType":"","amount2New":0,"dosageForm":"","sponsorNew":"BioNTech \/ Genmab","highestDevelopmentStatusID":null,"companyTruncated":"BioNTech \/.."},{"orgOrder":0,"company":"KaliVir Immunotherapeutics","sponsor":"Not Applicable","pharmaFlowCategory":"DU","amount":"Not Applicable","upfrontCash":"Not Applicable","newsHeadline":"KaliVir Immunotherapeutics Gets FDA Clearance for VET3-TGI Oncolytic Immunotherapy","therapeuticArea":"Oncology","highestDevelopmentStatus":"Phase I","country":"","productType":"Large molecule","productStatus":"New Molecular Entity","date":"July 2024","year":"2024","type":"Not Applicable","leadProduct":"Pembrolizumab","moa":"","url1":"","url2":"","graph1":null,"graph2":null,"graph3":"KaliVir Immunotherapeutics","amount2":0,"therapeuticAreaNew":null,"highestDevelopmentStatusNew":null,"highestDevelopmentShortName":null,"therapeuticAreaShortName":null,"productSubType":"","amount2New":0,"dosageForm":"","sponsorNew":"KaliVir Immunotherapeutics \/ Not Applicable","highestDevelopmentStatusID":null,"companyTruncated":"KaliVir Im.."},{"orgOrder":0,"company":"Merus","sponsor":"Merck & Co","pharmaFlowCategory":"DU","amount":"Not Applicable","upfrontCash":"Not Applicable","newsHeadline":"Merus Announces First Patient Dosed in Phase 2 Trial of Petosemtamab in 2L CRC","therapeuticArea":"Oncology","highestDevelopmentStatus":"Phase I\/ Phase II","country":"","productType":"Large molecule","productStatus":"New Molecular Entity","date":"July 2024","year":"2024","type":"Not Applicable","leadProduct":"Pembrolizumab","moa":"","url1":"","url2":"","graph1":null,"graph2":null,"graph3":"Merus","amount2":0,"therapeuticAreaNew":null,"highestDevelopmentStatusNew":null,"highestDevelopmentShortName":null,"therapeuticAreaShortName":null,"productSubType":"","amount2New":0,"dosageForm":"","sponsorNew":"Merus \/ Merck & Co","highestDevelopmentStatusID":null,"companyTruncated":"Merus \/ Me.."},{"orgOrder":0,"company":"Immutep","sponsor":"Not Applicable","pharmaFlowCategory":"DU","amount":"Not Applicable","upfrontCash":"Not Applicable","newsHeadline":"Immutep Reports Positive Results in Head and Neck SCC Patients with Negative PD-L1","therapeuticArea":"Oncology","highestDevelopmentStatus":"Phase II","country":"","productType":"Large molecule","productStatus":"New Molecular Entity","date":"July 2024","year":"2024","type":"Not Applicable","leadProduct":"Eftilagimod Alfa","moa":"","url1":"","url2":"","graph1":null,"graph2":null,"graph3":"Immutep","amount2":0,"therapeuticAreaNew":null,"highestDevelopmentStatusNew":null,"highestDevelopmentShortName":null,"therapeuticAreaShortName":null,"productSubType":"","amount2New":0,"dosageForm":"","sponsorNew":"Immutep \/ Not Applicable","highestDevelopmentStatusID":null,"companyTruncated":"Immutep \/ .."},{"orgOrder":0,"company":"Merck & Co","sponsor":"Pfizer Inc","pharmaFlowCategory":"DU","amount":"Not Applicable","upfrontCash":"Not Applicable","newsHeadline":"Merck Receives Positive EU CHMP Opinion for KEYTRUDA\u00ae Plus Padcev\u00ae in Urothelial Carcinoma","therapeuticArea":"Oncology","highestDevelopmentStatus":"Approved","country":"","productType":"Large molecule","productStatus":"Approved","date":"July 2024","year":"2024","type":"Not Applicable","leadProduct":"Pembrolizumab","moa":"","url1":"","url2":"","graph1":null,"graph2":null,"graph3":"Merck & Co","amount2":0,"therapeuticAreaNew":null,"highestDevelopmentStatusNew":null,"highestDevelopmentShortName":null,"therapeuticAreaShortName":null,"productSubType":"","amount2New":0,"dosageForm":"","sponsorNew":"Merck & Co \/ Pfizer Inc","highestDevelopmentStatusID":null,"companyTruncated":"Merck & Co.."},{"orgOrder":0,"company":"PDS Biotechnology","sponsor":"Not Applicable","pharmaFlowCategory":"DU","amount":"Not Applicable","upfrontCash":"Not Applicable","newsHeadline":"PDS Biotech Aligns with FDA on Phase 3 Trial in HPV16-Positive Head and Neck Cancer","therapeuticArea":"Oncology","highestDevelopmentStatus":"Phase II","country":"","productType":"Vaccine","productStatus":"New Molecular Entity","date":"August 2024","year":"2024","type":"Not Applicable","leadProduct":"PDS0101","moa":"","url1":"","url2":"","graph1":null,"graph2":null,"graph3":"PDS Biotechnology","amount2":0,"therapeuticAreaNew":null,"highestDevelopmentStatusNew":null,"highestDevelopmentShortName":null,"therapeuticAreaShortName":null,"productSubType":"","amount2New":0,"dosageForm":"","sponsorNew":"PDS Biotechnology \/ Not Applicable","highestDevelopmentStatusID":null,"companyTruncated":"PDS Biotec.."},{"orgOrder":0,"company":"Ultimovacs","sponsor":"Not Applicable","pharmaFlowCategory":"DU","amount":"Not Applicable","upfrontCash":"Not Applicable","newsHeadline":"Ultimovacs Announces Data from Phase II of UV1 and Pembrolizumab in Head and Neck Cancer","therapeuticArea":"Oncology","highestDevelopmentStatus":"Phase II","country":"","productType":"Vaccine","productStatus":"New Molecular Entity","date":"August 2024","year":"2024","type":"Not Applicable","leadProduct":"Pembrolizumab","moa":"","url1":"","url2":"","graph1":null,"graph2":null,"graph3":"Ultimovacs","amount2":0,"therapeuticAreaNew":null,"highestDevelopmentStatusNew":null,"highestDevelopmentShortName":null,"therapeuticAreaShortName":null,"productSubType":"","amount2New":0,"dosageForm":"","sponsorNew":"Ultimovacs \/ Not Applicable","highestDevelopmentStatusID":null,"companyTruncated":"Ultimovacs.."}]

    Find Clinical Drug Pipeline Developments & Deals for Keytruda

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                            01

                            Sanofi

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                            CPhI Worldwide, Milan
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                            • fda
                            • EDQM
                            • WHO-GMP
                            Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

                            Lead Product(s) : AMX-818,Pembrolizumab

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase I/ Phase II

                            Partner/Sponsor/Collaborator : Vir Biotechnology

                            Deal Size : Undisclosed

                            Deal Type : Licensing Agreement

                            DEALS_DEV arrow-down

                            Vir Biotechnology Expands with Worldwide License Agreement with Sanofi for T-cell Engagers

                            Details : Through the license agreement, Vir Biotechnology will gain the rights of three clinical-stage masked TCEs, which include SAR446309 (AMX-818) for the treatment of HER2-mutated Breast Neoplasms.

                            Product Name : SAR446309

                            Product Type : Cell and Gene therapy

                            Upfront Cash : Undisclosed

                            August 01, 2024

                            Lead Product(s) : AMX-818,Pembrolizumab

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase I/ Phase II

                            Partner/Sponsor/Collaborator : Vir Biotechnology

                            Deal Size : Undisclosed

                            Deal Type : Licensing Agreement

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                            02

                            Ultimovacs

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                            Pharmaconex 2024
                            Not Confirmed

                            Ultimovacs

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                            Pharmaconex 2024
                            Not Confirmed
                            • fda
                            • EDQM
                            • WHO-GMP
                            Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

                            Lead Product(s) : UV1,Pembrolizumab,Sargramostim

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase II

                            Partner/Sponsor/Collaborator : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

                            DEALS_DEV arrow-down

                            Ultimovacs Announces Data from Phase II of UV1 and Pembrolizumab in Head and Neck Cancer

                            Details : UV1 is a hTERT inhibitor, which is being evaluated in combination with pembrolizumab in patients for the treatment of metastatic or recurrent head and neck cancer.

                            Product Name : UV1

                            Product Type : Vaccine

                            Upfront Cash : Not Applicable

                            August 05, 2024

                            Lead Product(s) : UV1,Pembrolizumab,Sargramostim

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase II

                            Partner/Sponsor/Collaborator : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            03

                            Immutep

                            Australia arrow
                            Pharmaconex 2024
                            Not Confirmed

                            Immutep

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                            Not Confirmed
                            • fda
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                            • WHO-GMP
                            Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

                            Lead Product(s) : Eftilagimod Alfa,Pembrolizumab

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase II

                            Partner/Sponsor/Collaborator : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

                            DEALS_DEV arrow-down

                            Immutep Reports Positive Results in Head and Neck SCC Patients with Negative PD-L1

                            Details : IMP321 (Eftilagimod Alpha) is an APC activator protein, being investigated in combination with pembrolizumab as first-line treatment of recurrent or metastatic head & neck squamous cell carcinoma.

                            Product Name : Efti

                            Product Type : Large molecule

                            Upfront Cash : Not Applicable

                            July 11, 2024

                            Lead Product(s) : Eftilagimod Alfa,Pembrolizumab

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase II

                            Partner/Sponsor/Collaborator : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            04

                            Eisai

                            Japan arrow
                            Pharmaconex 2024
                            Not Confirmed

                            Eisai

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                            Pharmaconex 2024
                            Not Confirmed
                            • fda
                            • EDQM
                            • WHO-GMP
                            Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

                            Lead Product(s) : Pembrolizumab,Lenvatinib

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase II

                            Partner/Sponsor/Collaborator : Merck & Co

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

                            DEALS_DEV arrow-down

                            New Efficacy Data for KEYNOTE-B61 Added to LENVIMA® US Label for Advanced RCC

                            Details : Keytruda (Pembrolizumab) is a PD-1 inhibitor antibody, which is currently being evaluated in combination with lenvatinib for the first-line treatment of patients with advanced nccRCC.

                            Product Name : Keytruda

                            Product Type : Large molecule

                            Upfront Cash : Not Applicable

                            June 27, 2024

                            Lead Product(s) : Pembrolizumab,Lenvatinib

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase II

                            Partner/Sponsor/Collaborator : Merck & Co

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            05

                            Medicenna Therapeutics

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                            Pharmaconex 2024
                            Not Confirmed

                            Medicenna Therapeutics

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                            Pharmaconex 2024
                            Not Confirmed
                            • fda
                            • EDQM
                            • WHO-GMP
                            Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

                            Lead Product(s) : MDNA11,Pembrolizumab

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase I/ Phase II

                            Partner/Sponsor/Collaborator : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

                            DEALS_DEV arrow-down

                            Medicenna Receives EMA Approval to Expand Phase 1/2 ABILITY-1 Study to Europe

                            Details : MDNA11 is a IL-2 beta receptor super-agonist. It is being evaluated in combination with Keytruda for the treatment of solid tumor, renal cell carcinoma & triple negative breast cancer.

                            Product Name : MDNA11

                            Product Type : Large molecule

                            Upfront Cash : Not Applicable

                            June 26, 2024

                            Lead Product(s) : MDNA11,Pembrolizumab

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase I/ Phase II

                            Partner/Sponsor/Collaborator : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            06

                            Pfizer Inc

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                            Not Confirmed

                            Pfizer Inc

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                            Not Confirmed
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                            • WHO-GMP
                            Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

                            Lead Product(s) : Tisotumab Vedotin,Pembrolizumab,Carboplatin

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase II

                            Partner/Sponsor/Collaborator : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

                            DEALS_DEV arrow-down

                            Tisotumab Vedotin Phase 2 Shows Antitumor Activity in Recurrent Head and Neck Cancer

                            Details : Tivdak (tisotumab vedotin) is an ADC that acts as coagulation factor III binding agent & tubulin inhibitor. It is being evaluated for the treatment of Head and Neck Squamous Cell Carcinoma.

                            Product Name : Tivdak

                            Product Type : Large molecule

                            Upfront Cash : Not Applicable

                            June 03, 2024

                            Lead Product(s) : Tisotumab Vedotin,Pembrolizumab,Carboplatin

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase II

                            Partner/Sponsor/Collaborator : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            07

                            Strand Therapeutics

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                            Pharmaconex 2024
                            Not Confirmed

                            Strand Therapeutics

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                            Pharmaconex 2024
                            Not Confirmed
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                            • WHO-GMP
                            Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

                            Lead Product(s) : STX-001,Pembrolizumab

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase I/ Phase II

                            Partner/Sponsor/Collaborator : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

                            DEALS_DEV arrow-down

                            Strand doses first patient with mRNA Therapy STX-001 in Phase 1 solid tumor trial

                            Details : STX-001 is a novel programmable self-replicating mRNA encapsulated in lipid nanoparticles (LNPs), being evaluated for THE treatment of advanced solid tumors.

                            Product Name : STX-001

                            Product Type : Large molecule

                            Upfront Cash : Not Applicable

                            May 30, 2024

                            Lead Product(s) : STX-001,Pembrolizumab

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase I/ Phase II

                            Partner/Sponsor/Collaborator : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            08

                            Merus

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                            Pharmaconex 2024
                            Not Confirmed

                            Merus

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                            Not Confirmed
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                            • WHO-GMP
                            Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

                            Lead Product(s) : Petosemtamab,Pembrolizumab

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase I/ Phase II

                            Partner/Sponsor/Collaborator : Jefferies

                            Deal Size : $400.2 million

                            Deal Type : Public Offering

                            DEALS_DEV arrow-down

                            Merus Announces Pricing of Upsized Public Offering of Common Shares

                            Details : Merus will use the proceeds to advance the clinical development of its candidates, including MCLA-158 (petosemtamab), a Biclonics® low-fucose human full-length IgG1 antibody targeting the EGFR.

                            Product Name : MCLA-158

                            Product Type : Large molecule

                            Upfront Cash : Undisclosed

                            May 29, 2024

                            Lead Product(s) : Petosemtamab,Pembrolizumab

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase I/ Phase II

                            Partner/Sponsor/Collaborator : Jefferies

                            Deal Size : $400.2 million

                            Deal Type : Public Offering

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                            09

                            Immunocore

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                            Pharmaconex 2024
                            Not Confirmed

                            Immunocore

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                            Pharmaconex 2024
                            Not Confirmed
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                            • WHO-GMP
                            Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

                            Lead Product(s) : Tebentafusp,Pembrolizumab

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase III

                            Partner/Sponsor/Collaborator : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

                            DEALS_DEV arrow-down

                            Immunocore Converts TEBE-AM Trial to Registrational Phase 3 for KIMMTRAK in Melanoma

                            Details : Kimmtrak (tebentafusp) is a novel bispecific protein comprised of a soluble T cell receptor fused to an anti-CD3 immune-effector function. It is being investigated for Malignant Melanoma, Cutaneous.

                            Product Name : Kimmtrak

                            Product Type : Large molecule

                            Upfront Cash : Not Applicable

                            May 29, 2024

                            Lead Product(s) : Tebentafusp,Pembrolizumab

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase III

                            Partner/Sponsor/Collaborator : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            10

                            Merck & Co

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                            Pharmaconex 2024
                            Not Confirmed

                            Merck & Co

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                            Pharmaconex 2024
                            Not Confirmed
                            • fda
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                            Lead Product(s) : Pembrolizumab,Carboplatin,Paclitaxel

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase III

                            Partner/Sponsor/Collaborator : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            Merck’s KEYNOTE-522 Trial Meets Survival Endpoint in High-Risk TNBC Patients

                            Details : Keytruda (pembrolizumab), anti-PD-1 therapy, met its endpoint, in combination with chemotherapy for the treatment of patients with high-risk early-stage triple-negative breast cancer.

                            Product Name : Keytruda

                            Product Type : Large molecule

                            Upfront Cash : Not Applicable

                            May 28, 2024

                            Lead Product(s) : Pembrolizumab,Carboplatin,Paclitaxel

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase III

                            Partner/Sponsor/Collaborator : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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