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    Find Clinical Drug Pipeline Developments & Deals by Bristol Myers Squibb

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                            01

                            Bristol Myers Squibb

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                            Bristol Myers Squibb

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                            Lead Product(s) : T-Cell-based Therapy

                            Therapeutic Area : Hematology

                            Study Phase : Preclinical

                            Recipient : Prime Medicine

                            Deal Size : $3,610.0 million

                            Deal Type : Collaboration

                            DEALS_DEV arrow-down

                            BMS Pays Prime $110M to Form T-cell Therapy Pact

                            Details : Prime Medicine will design optimized Prime Editor reagents for a select number of targets, including reagents that use its Prime Assisted Site-Specific Integrase Gene Editing (PASSIGE™) technology.

                            Brand Name : Undisclosed

                            Molecule Type : Cell and Gene therapy

                            Upfront Cash : $110.0 million

                            September 30, 2024

                            Lead Product(s) : T-Cell-based Therapy

                            Therapeutic Area : Hematology

                            Highest Development Status : Preclinical

                            Recipient : Prime Medicine

                            Deal Size : $3,610.0 million

                            Deal Type : Collaboration

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                            02

                            Bristol Myers Squibb

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                            Lead Product(s) : Idecabtagene Vicleucel,Lenalidomide,Fludarabine Phosphate

                            Therapeutic Area : Oncology

                            Study Phase : Phase III

                            Sponsor : 2Seventy Bio

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            Bristol Myers Squibb and 2seventy bio Update on KarMMa-9 Trial of Abecma in Myeloma

                            Details : Abecma (idecabtagene vicleucel) is a CAR T cell therapy which binds to BCMA on the surface of multiple myeloma cells. It is being evaluated for newly diagnosed multiple myeloma.

                            Brand Name : Abecma

                            Molecule Type : Cell and Gene therapy

                            Upfront Cash : Not Applicable

                            September 25, 2024

                            Lead Product(s) : Idecabtagene Vicleucel,Lenalidomide,Fludarabine Phosphate

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase III

                            Sponsor : 2Seventy Bio

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            03

                            Bristol Myers Squibb

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                            Lead Product(s) : Mavacamten

                            Therapeutic Area : Cardiology/Vascular Diseases

                            Study Phase : Approved

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

                            DEALS_DEV arrow-down

                            CAMZYOS® Phase 3 Data Confirms Efficacy in Obstructive Hypertrophic Cardiomyopathy

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

                            Brand Name : Camzyos

                            Molecule Type : Small molecule

                            Upfront Cash : Not Applicable

                            September 01, 2024

                            Lead Product(s) : Mavacamten

                            Therapeutic Area : Cardiology/Vascular Diseases

                            Highest Development Status : Approved

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            04

                            Bristol Myers Squibb

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                            Lead Product(s) : Nivolumab,Ipilimumab

                            Therapeutic Area : Oncology

                            Study Phase : Phase III

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            Bristol Myers Squibb Receives EMA Validation for Opdivo and Yervoy in Liver Cancer

                            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.

                            Brand Name : Opdivo

                            Molecule Type : Large molecule

                            Upfront Cash : Not Applicable

                            July 19, 2024

                            Lead Product(s) : Nivolumab,Ipilimumab

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase III

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            05

                            Bristol Myers Squibb

                            U.S.A arrow
                            euroPLX 86 Munich
                            Not Confirmed

                            Bristol Myers Squibb

                            U.S.A arrow
                            euroPLX 86 Munich
                            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) : Farletuzumab Ecteribulin

                            Therapeutic Area : Oncology

                            Study Phase : Phase I/ Phase II

                            Recipient : Eisai

                            Deal Size : $3,100.0 million

                            Deal Type : Termination

                            DEALS_DEV arrow-down

                            Japan's Eisai Terminates ADC Manufacturing Pact with BMS

                            Details : With the termination of its agreement with BMS, Eisai will solely focus on the development & commercialization of MORAb-202 (farletuzumab ecteribulin), is being evaluated for the treatment of NSCLC.

                            Brand Name : MORAb-202

                            Molecule Type : Large molecule

                            Upfront Cash : $650.0 million

                            July 01, 2024

                            Lead Product(s) : Farletuzumab Ecteribulin

                            Therapeutic Area : Oncology

                            Highest Development Status : Phase I/ Phase II

                            Recipient : Eisai

                            Deal Size : $3,100.0 million

                            Deal Type : Termination

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                            06

                            Bristol Myers Squibb

                            U.S.A arrow
                            euroPLX 86 Munich
                            Not Confirmed

                            Bristol Myers Squibb

                            U.S.A arrow
                            euroPLX 86 Munich
                            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) : Adagrasib,Cetuximab

                            Therapeutic Area : Oncology

                            Study Phase : Approved

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

                            DEALS_DEV arrow-down

                            Bristol Myers Squibb Announces FDA Approval of KRAZATI with Cetuximab for CRC

                            Details : KRAZATI (adagrasib), a potent oral small-molecule inhibitor of KRASG12C, is indicated in combination with cetuximab for patients with locally advanced or metastatic colorectal cancer.

                            Brand Name : Krazati

                            Molecule Type : Small molecule

                            Upfront Cash : Not Applicable

                            June 21, 2024

                            Lead Product(s) : Adagrasib,Cetuximab

                            Therapeutic Area : Oncology

                            Highest Development Status : Approved

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            07

                            Bristol Myers Squibb

                            U.S.A arrow
                            euroPLX 86 Munich
                            Not Confirmed

                            Bristol Myers Squibb

                            U.S.A arrow
                            euroPLX 86 Munich
                            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

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

                            DEALS_DEV arrow-down

                            BMS: Opdivo + Yervoy Improve Survival in Advanced Hepatocellular Carcinoma

                            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.

                            Brand Name : Opdivo

                            Molecule Type : Large molecule

                            Upfront Cash : Not Applicable

                            June 04, 2024

                            Lead Product(s) : Nivolumab,Ipilimumab

                            Therapeutic Area : Oncology

                            Highest Development Status : Approved

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            08

                            Bristol Myers Squibb

                            U.S.A arrow
                            euroPLX 86 Munich
                            Not Confirmed

                            Bristol Myers Squibb

                            U.S.A arrow
                            euroPLX 86 Munich
                            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

                            Sponsor : Netherlands Cancer Institute

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

                            DEALS_DEV arrow-down

                            Pre-Surgery Bristol Myers Combination Therapy Improves Skin Cancer Outcomes

                            Details : Opdivo (Nivolumab) and Yervoy (Ipilimumab) IV infusion, when given prior to surgery whose skin cancer had spread to lymph nodes, had better outcomes than those who did not get the drugs.

                            Brand Name : Opdivo

                            Molecule Type : Large molecule

                            Upfront Cash : Not Applicable

                            June 03, 2024

                            Lead Product(s) : Nivolumab,Ipilimumab

                            Therapeutic Area : Oncology

                            Highest Development Status : Approved

                            Sponsor : Netherlands Cancer Institute

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            09

                            Bristol Myers Squibb

                            U.S.A arrow
                            euroPLX 86 Munich
                            Not Confirmed

                            Bristol Myers Squibb

                            U.S.A arrow
                            euroPLX 86 Munich
                            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,Cisplatin,Gemcitabine

                            Therapeutic Area : Oncology

                            Study Phase : Approved

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

                            DEALS_DEV arrow-down

                            BMS Receives EU Approval for Opdivo® with Cisplatin and Gemcitabine in Urothelial Cancer

                            Details : Opdivo (nivolumab) is a PD-1 immune checkpoint inhibitor, which is approved in combination with cisplatin and gemcitabine, for the patients with unresectable or metastatic urothelial carcinoma.

                            Brand Name : Opdivo

                            Molecule Type : Large molecule

                            Upfront Cash : Not Applicable

                            May 29, 2024

                            Lead Product(s) : Nivolumab,Cisplatin,Gemcitabine

                            Therapeutic Area : Oncology

                            Highest Development Status : Approved

                            Sponsor : Not Applicable

                            Deal Size : Not Applicable

                            Deal Type : Not Applicable

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                            10

                            Bristol Myers Squibb

                            U.S.A arrow
                            euroPLX 86 Munich
                            Not Confirmed

                            Bristol Myers Squibb

                            U.S.A arrow
                            euroPLX 86 Munich
                            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) : PRX019

                            Therapeutic Area : Neurology

                            Study Phase : IND Enabling

                            Recipient : Prothena

                            Deal Size : $2,200.0 million

                            Deal Type : Licensing Agreement

                            DEALS_DEV arrow-down

                            Prothena Announces Bristol Myers Squibb Opt-in for Global License of PRX019 Program

                            Details : Under the agreement, Bristol will have the exclusive global license to PRX019, a potential treatment of neurodegenerative diseases with an undisclosed target.

                            Brand Name : PRX019

                            Molecule Type : Large molecule

                            Upfront Cash : $150.0 million

                            May 28, 2024

                            Lead Product(s) : PRX019

                            Therapeutic Area : Neurology

                            Highest Development Status : IND Enabling

                            Recipient : Prothena

                            Deal Size : $2,200.0 million

                            Deal Type : Licensing Agreement

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