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Squibb","sponsor":"Inapplicable","pharmaFlowCategory":"DU","therapeuticArea":"Oncology","country":"U.S.A","productType":"Cell and Gene therapy","year":"2020","type":"Inapplicable","leadProduct":"Lisocabtagene Maraleucel","moa":"CD19","graph1":"Oncology","graph2":"Phase I\/ Phase II","graph3":"Bristol Myers Squibb","amount2":0,"highestDevelopmentShortName":"Ph I\/II","therapeuticAreaShortName":"Oncology","amount2New":0,"dosageForm":"Undisclosed","sponsorNew":"Bristol Myers Squibb \/ Inapplicable","highestDevelopmentStatusID":"7","companyTruncated":"Bristol Myers Squibb \/ Inapplicable"},{"orgOrder":0,"company":"Bristol Myers Squibb","sponsor":"Inapplicable","pharmaFlowCategory":"DU","therapeuticArea":"Oncology","country":"U.S.A","productType":"Cell and Gene therapy","year":"2024","type":"Inapplicable","leadProduct":"Lisocabtagene Maraleucel","moa":"CD19","graph1":"Oncology","graph2":"Approved FDF","graph3":"Bristol Myers Squibb","amount2":0,"highestDevelopmentShortName":"Approved 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Inapplicable"},{"orgOrder":0,"company":"Bristol Myers Squibb","sponsor":"Inapplicable","pharmaFlowCategory":"DU","therapeuticArea":"Oncology","country":"U.S.A","productType":"Antibody","year":"2025","type":"Inapplicable","leadProduct":"Nivolumab","moa":"||PD-1","graph1":"Oncology","graph2":"Approved FDF","graph3":"Bristol Myers Squibb","amount2":0,"highestDevelopmentShortName":"Approved FDF","therapeuticAreaShortName":"Oncology","amount2New":0,"dosageForm":"Intravenous Infusion","sponsorNew":"Bristol Myers Squibb \/ Inapplicable","highestDevelopmentStatusID":"15","companyTruncated":"Bristol Myers Squibb \/ Inapplicable"},{"orgOrder":0,"company":"Bristol Myers Squibb","sponsor":"Tubulis","pharmaFlowCategory":"D","therapeuticArea":"Oncology","country":"GERMANY","productType":"Antibody-drug Conjugate","year":"2025","type":"Licensing Agreement","leadProduct":"Undisclosed","moa":"Undisclosed","graph1":"Oncology","graph2":"Phase I","graph3":"Bristol Myers Squibb","amount2":1.02,"highestDevelopmentShortName":"Ph I","therapeuticAreaShortName":"Oncology","amount2New":1.02,"dosageForm":"Undisclosed","sponsorNew":"Bristol Myers Squibb \/ Bristol Myers Squibb","highestDevelopmentStatusID":"6","companyTruncated":"Bristol Myers Squibb \/ Bristol Myers Squibb"},{"orgOrder":0,"company":"Bristol Myers Squibb","sponsor":"BioNTech","pharmaFlowCategory":"D","therapeuticArea":"Oncology","country":"GERMANY","productType":"Antibody","year":"2025","type":"Partnership","leadProduct":"BNT327","moa":"||PD-1\/VEGF","graph1":"Oncology","graph2":"Phase III","graph3":"Bristol Myers Squibb","amount2":11.1,"highestDevelopmentShortName":"Ph III","therapeuticAreaShortName":"Oncology","amount2New":11.1,"dosageForm":"Intravenous Infusion","sponsorNew":"Bristol Myers Squibb \/ Bristol Myers Squibb","highestDevelopmentStatusID":"10","companyTruncated":"Bristol Myers Squibb \/ Bristol Myers Squibb"}]

    Find Clinical Drug Pipeline Developments & Deals by Bristol Myers Squibb

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                            01

                            Bristol Myers Squibb

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                            Lead Product(s) : BNT327,Etoposide,Carboplatin

                            Therapeutic Area : Oncology

                            Study Phase : Phase III

                            Recipient : BioNTech

                            Deal Size : $11,100.0 million

                            Deal Type : Partnership

                            DEALS_DEV arrow-down

                            BioNTech and BMS Partner to Develop Bispecific Antibody BNT327 for Solid Tumors

                            Details : The partnership aims to expand BioNTech’s BNT327, a next-generation bispecific antibody candidate targeting PD-L1 and VEGF-A, is currently being evaluated in 1L-treatment in extensive stage SCLC.

                            Product Name : BNT327

                            Product Type : Antibody

                            Upfront Cash : $1500 million

                            June 02, 2025

                            Lead Product(s) : BNT327,Etoposide,Carboplatin

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase III

                            Recipient : BioNTech

                            Deal Size : $11,100.0 million

                            Deal Type : Partnership

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                            02

                            Bristol Myers Squibb

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                            Lead Product(s) : Nivolumab,Cisplatin,Gemcitabine

                            Therapeutic Area : Oncology

                            Study Phase : Approved FDF

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            BMS Gets EU Nod for Opdivo Combo in High-Risk Resectable NSCLC with PD-L1+

                            Details : Opdivo (nivolumab) a PD-1 inihibitor in combination with chemotherapy is indicated for the treatment of adult patients with resectable non-small cell lung cancer.

                            Product Name : Opdivo

                            Product Type : Antibody

                            Upfront Cash : Inapplicable

                            May 16, 2025

                            Lead Product(s) : Nivolumab,Cisplatin,Gemcitabine

                            Therapeutic Area : Oncology

                            Highest Development Status : Approved FDF

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            03

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                            Lead Product(s) : Mavacamten

                            Therapeutic Area : Cardiology/Vascular Diseases

                            Study Phase : Approved FDF

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

                            DEALS_DEV arrow-down

                            FDA Updates CAMZYOS Label to Ease Echo Monitoring and Lower Contraindications

                            Details : Camzyos (mavacamten) is a cardiac myosin inhibitor, indicated for treatment of adults with class II-III non-obstructive hypertrophic cardiomyopathy.

                            Product Name : Camzyos

                            Product Type : Other Small Molecule

                            Upfront Cash : Inapplicable

                            April 17, 2025

                            Lead Product(s) : Mavacamten

                            Therapeutic Area : Cardiology/Vascular Diseases

                            Highest Development Status : Approved FDF

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            04

                            Bristol Myers Squibb

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                            Lead Product(s) : Mavacamten

                            Therapeutic Area : Cardiology/Vascular Diseases

                            Study Phase : Phase III

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            Bristol Myers Squibb Provides Update on Phase 3 ODYSSEY-HCM Trial

                            Details : Camzyos (mavacamten) is a cardiac myosin inhibitor, being investigated for treatment of adults with class II-III non-obstructive hypertrophic cardiomyopathy.

                            Product Name : Camzyos

                            Product Type : Other Small Molecule

                            Upfront Cash : Inapplicable

                            April 14, 2025

                            Lead Product(s) : Mavacamten

                            Therapeutic Area : Cardiology/Vascular Diseases

                            Highest Development Status : Phase III

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            05

                            Bristol Myers Squibb

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                            Lead Product(s) : Nivolumab,Cisplatin,Gemcitabine

                            Therapeutic Area : Oncology

                            Study Phase : Approved FDF

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            BMS Gets Positive CHMP Opinion for Perioperative Opdivo + Chemo in NSCLC

                            Details : Opdivo (nivolumab) a PD-1 inihibitor in combination with chemotherapy is indicated for the treatment of adult patients with resectable non-small cell lung cancer.

                            Product Name : Opdivo

                            Product Type : Antibody

                            Upfront Cash : Inapplicable

                            March 28, 2025

                            Lead Product(s) : Nivolumab,Cisplatin,Gemcitabine

                            Therapeutic Area : Oncology

                            Highest Development Status : Approved FDF

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            06

                            Bristol Myers Squibb

                            U.S.A arrow
                            AGGSpend
                            Not Confirmed

                            Bristol Myers Squibb

                            U.S.A arrow
                            AGGSpend
                            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) : Nivolumab,Hyaluronidase

                            Therapeutic Area : Oncology

                            Study Phase : Approved FDF

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

                            DEALS_DEV arrow-down

                            BMS Gets Positive CHMP Opinion for Subcutaneous Opdivo in Solid Tumors

                            Details : Opdivo Qvantig (nivolumab & hyaluronidase) subcutaneous version PD-1 inhibitor is indicated for the treatment of carcinoma, renal cell.

                            Product Name : Opdivo Qvantig

                            Product Type : Antibody

                            Upfront Cash : Inapplicable

                            March 28, 2025

                            Lead Product(s) : Nivolumab,Hyaluronidase

                            Therapeutic Area : Oncology

                            Highest Development Status : Approved FDF

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            07

                            Bristol Myers Squibb

                            U.S.A arrow
                            AGGSpend
                            Not Confirmed

                            Bristol Myers Squibb

                            U.S.A arrow
                            AGGSpend
                            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) : Nivolumab,Ipilimumab

                            Therapeutic Area : Oncology

                            Study Phase : Approved FDF

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

                            DEALS_DEV arrow-down

                            BMS Receives EC Approval for Opdivo® (nivolumab) Plus Yervoy® (ipilimumab)

                            Details : Combination of Opdivo (nivolumab) and Yervoy(Ipilimumab) is approved and indicated as an initial treatment for patients with advanced hepatocellular carcinoma.

                            Product Name : Opdivo

                            Product Type : Antibody

                            Upfront Cash : Inapplicable

                            March 07, 2025

                            Lead Product(s) : Nivolumab,Ipilimumab

                            Therapeutic Area : Oncology

                            Highest Development Status : Approved FDF

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            08

                            Bristol Myers Squibb

                            U.S.A arrow
                            AGGSpend
                            Not Confirmed

                            Bristol Myers Squibb

                            U.S.A arrow
                            AGGSpend
                            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) : Nivolumab,Ipilimumab

                            Therapeutic Area : Oncology

                            Study Phase : Approved FDF

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

                            DEALS_DEV arrow-down

                            CHMP Backs Opdivo + Yervoy for Advanced Liver Cancer Treatment

                            Details : Combination of Opdivo (nivolumab) and Yervoy(Ipilimumab) met the main goal of a late-stage study evaluating it as an initial treatment for patients with advanced hepatocellular carcinoma.

                            Product Name : Opdivo

                            Product Type : Antibody

                            Upfront Cash : Inapplicable

                            January 31, 2025

                            Lead Product(s) : Nivolumab,Ipilimumab

                            Therapeutic Area : Oncology

                            Highest Development Status : Approved FDF

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            09

                            Bristol Myers Squibb

                            U.S.A arrow
                            AGGSpend
                            Not Confirmed

                            Bristol Myers Squibb

                            U.S.A arrow
                            AGGSpend
                            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) : Repotrectinib

                            Therapeutic Area : Oncology

                            Study Phase : Approved FDF

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

                            DEALS_DEV arrow-down

                            Bristol Myers Receives CHMP Opinion for Repotrectinib in ROS1/NTRK Tumors

                            Details : Augtyro (repotrectinib) is a next-generation tyrosine kinase inhibitor (TKI), for the treatment of locally advanced or metastatic ROS1-positive non-small cell lung cancer (NSCLC).

                            Product Name : Augtyro

                            Product Type : Other Small Molecule

                            Upfront Cash : Inapplicable

                            November 15, 2024

                            Lead Product(s) : Repotrectinib

                            Therapeutic Area : Oncology

                            Highest Development Status : Approved FDF

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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                            10

                            Bristol Myers Squibb

                            U.S.A arrow
                            AGGSpend
                            Not Confirmed

                            Bristol Myers Squibb

                            U.S.A arrow
                            AGGSpend
                            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) : Nivolumab,Ipilimumab

                            Therapeutic Area : Oncology

                            Study Phase : Phase III

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

                            DEALS_DEV arrow-down

                            Bristol Myers Squibb Provides Update on Phase 3 CheckMate -73L Trial

                            Details : Opdivo (nivolumab) in combination with Yervoy (ipilimumab) is being evaluated in phase 3 clinical development for the treatment of unresectable, locally advanced stage III non-small cell lung cancer.

                            Product Name : Opdivo

                            Product Type : Antibody

                            Upfront Cash : Inapplicable

                            October 05, 2024

                            Lead Product(s) : Nivolumab,Ipilimumab

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase III

                            Sponsor : Inapplicable

                            Deal Size : Inapplicable

                            Deal Type : Inapplicable

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