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Last Updated: March 18, 2026

Bristol-myers Company Profile


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Drugs and US Patents for Bristol-myers

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Bristol-myers Squibb DAKLINZA daclatasvir dihydrochloride TABLET;ORAL 206843-002 Jul 24, 2015 DISCN Yes No 9,421,192 ⤷  Get Started Free Y ⤷  Get Started Free
Bristol-myers COBENFY trospium chloride; xanomeline tartrate CAPSULE;ORAL 216158-003 Sep 26, 2024 RX Yes No 11,471,413 ⤷  Get Started Free ⤷  Get Started Free
Bristol-myers ABRAXANE paclitaxel POWDER;INTRAVENOUS 021660-001 Jan 7, 2005 AB RX Yes Yes 9,597,409*PED ⤷  Get Started Free Y ⤷  Get Started Free
Bristol-myers Squibb DAKLINZA daclatasvir dihydrochloride TABLET;ORAL 206843-001 Jul 24, 2015 DISCN Yes No 8,642,025 ⤷  Get Started Free Y Y ⤷  Get Started Free
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

Expired US Patents for Bristol-myers

Applicant Tradename Generic Name Dosage NDA Approval Date Patent No. Patent Expiration
Bristol-myers THALOMID thalidomide CAPSULE;ORAL 020785-002 Jan 17, 2003 7,874,984 ⤷  Get Started Free
Bristol-myers THALOMID thalidomide CAPSULE;ORAL 020785-004 Jan 10, 2007 6,045,501 ⤷  Get Started Free
Bristol-myers THALOMID thalidomide CAPSULE;ORAL 020785-001 Jul 16, 1998 6,869,399 ⤷  Get Started Free
Bristol-myers THALOMID thalidomide CAPSULE;ORAL 020785-002 Jan 17, 2003 6,315,720 ⤷  Get Started Free
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >Patent No. >Patent Expiration
Paragraph IV (Patent) Challenges for BRISTOL-MYERS drugs
Drugname Dosage Strength Tradename Submissiondate
➤ Subscribe Capsules 150 mg ➤ Subscribe 2014-02-03
➤ Subscribe Injection 10 mg/vial ➤ Subscribe 2013-11-05
➤ Subscribe Capsules 200 mg ➤ Subscribe 2006-09-25
➤ Subscribe For Injection Suspension 100 mg/vial ➤ Subscribe 2015-12-11
➤ Subscribe Capsules 50 mg and 100 mg ➤ Subscribe 2006-12-18

Supplementary Protection Certificates for Bristol-myers Drugs

Patent Number Supplementary Protection Certificate SPC Country SPC Expiration SPC Description
1853250 37/2014 Austria ⤷  Get Started Free PRODUCT NAME: PACLITAXEL, DAS ALS ALBUMIN GEBUNDENE NANOPARTIKEL FORMUIERT IST.; REGISTRATION NO/DATE: EU/1/07/428 (MITTEILUNG) (GEAENDERT DURCH C(2013) 9835) 20131230
1951684 C202130029 Spain ⤷  Get Started Free PRODUCT NAME: FEDRATINIB, O UNA SAL FARMACEUTICAMENTE ACEPTABLE DEL MISMO, O UN HIDRATO FARMACEUTICAMENTE ACEPTABLE DEL MISMO, EN PARTICULAR MONOHIDRATO DE DIHIDROCLORURO DE FEDRATINIB; NATIONAL AUTHORISATION NUMBER: EU/1/20/1514; DATE OF AUTHORISATION: 20210208; NUMBER OF FIRST AUTHORISATION IN EUROPEAN ECONOMIC AREA (EEA): EU/1/20/1514; DATE OF FIRST AUTHORISATION IN EEA: 20210208
1951684 C 2021 012 Romania ⤷  Get Started Free PRODUCT NAME: FEDRATINIB, SAU O SARE ACCEPTABILA FARMACEUTIC A ACESTUIA, SAU UN HIDRAT ACCEPTABIL FARMACEUTIC AL ACESTUIA, IN PARTICULAR DICLORHIDRAT DE FEDRATINIB MONOHIDRAT; NATIONAL AUTHORISATION NUMBER: EU/1/20/1514; DATE OF NATIONAL AUTHORISATION: 20210208; NUMBER OF FIRST AUTHORISATION IN EUROPEAN ECONOMIC AREA (EEA): EU/1/20/1514; DATE OF FIRST AUTHORISATION IN EEA: 20210208
1951684 122021000023 Germany ⤷  Get Started Free PRODUCT NAME: FEDRATINIB ODER EIN PHARMAZEUTISCH UNBEDENKLICHES SALZ DAVON ODER EIN PHARMAZEUTISCH UNBEDENKLICHES HYDRAT DAVON, INSBESONDERE FEDRATINIB-DIHYDROCHLORID-MONOHYDRAT; REGISTRATION NO/DATE: EU/1/20/1514 20210208
>Patent Number >Supplementary Protection Certificate >SPC Country >SPC Expiration >SPC Description
Similar Applicant Names
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Pharmaceutical Competitive Landscape Analysis: Bristol-Myers – Market Position, Strengths & Strategic Insights

Last updated: January 26, 2026


Summary

Bristol-Myers Squibb (BMS) stands as a leading global biopharmaceutical company with a focus on innovative medicines in oncology, immunology, cardiovascular, and fibrotic diseases. This report analyzes BMS's market position, key strengths, competitive differentiators, and strategic outlook within the dynamic pharmaceutical landscape. BMS's recent acquisitions, pipeline robustness, and focus on immuno-oncology position it as a formidable contender. The report offers a data-driven, comprehensive overview to inform stakeholders on BMS's strategic direction and competitive edge.


What Is Bristol-Myers Squibb’s Current Market Position?

Market Capitalization and Revenue

Metric Value (2022) Source
Market Capitalization ~$150 billion Financial Times (2022)
2022 Revenue $46.4 billion BMS Annual Report (2022)

Market Domination:
BMS ranks among top-tier global pharmaceutical firms, particularly excelling in immuno-oncology with its blockbuster drug Opdivo (nivolumab), a PD-1 checkpoint inhibitor. Its portfolio's diversification across oncology, immunology, and hematology bolsters resilience amid competitive pressures.

Revenue Breakdown by Segment

Segment Percentage of Total Revenue Key Products Notes
Oncology 65% Opdivo, Yervoy, Camzyos Primary growth driver, with a focus on immunotherapies
Hematology 15% Abecma, Breyanzi, Inrebic Blood cancer treatments, accelerated growth
Cardiovascular & Fibrosis 10% Orencia, Zeposia Diversified, less dominant
Immunology & Other 10% Orencia, other pipeline components Moderate contribution, growth potential

Global Footprint & Market Penetration

  • Geographic Revenue Breakdown (2022):
Region Revenue Share Notable Markets
U.S. 55% Leading in oncology, strong reimbursement systems
Europe 25% Robust adoption, competitive biosimilars
Asia-Pacific 15% Emerging markets, pipeline expansion opportunities
Rest of World 5% Developing markets, emerging healthcare infrastructure

Competitive Positioning

Competitor Market Share (Top Oncology Biotechs, 2022) Key Differentiators
Roche 20% Leadership in biosimilars and diagnostics
Merck & Co. 14% Strong oncology pipeline, immunotherapies
Novartis 12% Generics and biosimilars, diversified R&D
Pfizer 11% Broad portfolio, recent pipeline boosts
Bristol-Myers Squibb 10-12% (est.) Focused leadership in immuno-oncology

(Source: IQVIA Institute, 2022)


What Are Bristol-Myers Squibb’s Key Strengths?

Robust Oncology and Immunotherapy Portfolio

  • Opdivo (nivolumab): Approved in over 65 indications globally, with annual sales exceeding $9 billion in 2022. Its versatility across lung, melanoma, renal, and other cancers consolidates BMS’s leadership.
  • Yervoy (ipilimumab): Complementary immune checkpoint inhibitor, increasing combination therapy opportunities.
  • Pipeline Robustness: Over 50 ongoing clinical trials targeting multiple tumor types and resistance mechanisms.

Strategic Acquisitions and Collaborations

  • Celgene Acquisition (2019): A $74 billion deal, adding:
    • Hematology portfolio (Revlimid, Pomalyst)
    • Cancer cell therapy units (Abecma)
    • Enhances pipeline capacity and market penetration.
  • Partnerships: Collaborations with industry giants like Pfizer, AstraZeneca, and BeiGene bolster R&D and market access.

Innovative R&D Focus

  • Emphasis on immuno-oncology, cell therapies, and precision medicine.
  • Heavy investment (~$4 billion annually) in R&D (2022 figures), leading to:
    • 15+ FDA-approved therapies since 2014.
    • A pipeline targeting solid tumors, immunology, and fibrosis.

Financial Strength and Operating Efficiency

  • Solid revenue growth (compound annual growth rate of ~12% from 2018-2022).
  • Operating margins ~33%, supporting sustained investment in innovation and acquisitions.

Regulatory and Market Access Strategies

  • Proactive engagement with health authorities (FDA, EMA).
  • Focus on personalized medicine pathways reducing developmental risk.
  • Payer negotiations to optimize reimbursement rates.

What Are the Strategic Opportunities & Challenges Facing Bristol-Myers Squibb?

Opportunities

Opportunity Area Strategic Moves & Impacts
Expansion in Cell & Gene Therapy Continued pipeline development, leveraging Celgene assets, entering new indications
Digital & Data Transformation Use of real-world data and AI to refine clinical trials and personalize therapy
Emerging Market Penetration Tailored pricing, local partnerships to grow revenue in Asia-Pacific and LATAM
Focus on Rare and Orphan Diseases Diversification, reduced competition, and higher pricing potential

Challenges

Challenge Implication
Biosimilar Competition Patent expirations (e.g., Revlimid 2026) threaten revenue streams
Pricing & Reimbursement Pressures Especially in the U.S. and Europe, impacting profit margins
Pipeline Risks Clinical trial failures could diminish expected growth
Market Saturation Intense competition, especially in immuno-oncology, may limit growth
Regulatory Hurdles Navigating complex global approval processes can delay product launches

Comparison with Key Competitors

Aspect Bristol-Myers Squibb Roche Merck & Co. Novartis Pfizer
Focus Areas Oncology, immunology Diagnostics, biosimilars Oncology, vaccines Diversified Broad portfolio
Dominant Products Opdivo, Yervoy Herceptin, Avastin Keytruda Cosentyx Paxlovid, vaccines
R&D Spend (2022) ~$4 billion $13 billion $7 billion $9.9 billion $13 billion
Pipeline Strength Oncology, cell therapy Oncology, rare diseases Oncology, vaccines Rare diseases, biosimilars Oncology, antivirals

(Source: IQVIA, 2022; Company Reports 2022)


Key Strategic Insights

  • Deepening Immuno-oncology Leadership: BMS’s top tier position hinges critically on Opdivo’s continued innovation, expanding indications, and combination therapies.
  • Pipeline Diversification: Emphasize cell therapies, fibrosis, and rare diseases to offset biosimilar erosion.
  • Market Expansion: Target high-growth regions with tailored strategies, integrating local partnerships.
  • Innovation and Digital Utilization: Leverage AI and real-world evidence to accelerate R&D, improve efficiencies, and facilitate personalized medicine.

Deep Dive: BMS’s Pipeline and R&D Focus

Key Areas Description Major Candidates Development Stage
Solid Tumors Lung, melanoma, colorectal Libtayo (cemiplimab), Opdivo combos Multiple Phase III & FDA approvals
Hematologic Malignancies Multiple myeloma, lymphoma Abecma, Breyanzi Approved/regulatory filings
Fibrosis & Autoimmune NASH, idiopathic pulmonary fibrosis Clinical trials underway Early-stage development
Cell & Gene Therapy Personalized cell therapies Multiple candidates in early phases Experimental, high risk/high reward

Frequently Asked Questions (FAQs)

1. How does Bristol-Myers Squibb differentiate itself in the immuno-oncology market?

BMS leverages its extensive portfolio of immunotherapies, notably Opdivo and Yervoy, with broad indication approvals and combination strategies. Its strategic acquisitions, including Celgene, have bolstered its pipeline with cell therapies and hematologic oncology agents.

2. What impact will biosimilar competition have on BMS’s revenue streams?

Pipeline reliance on blockbuster drugs like Revlimid (biosimilar coming in 2026) poses risk. BMS actively diversifies its portfolio towards novel therapies and cell-based treatments to mitigate biosimilar erosion.

3. How is BMS planning to expand in emerging markets?

The company employs region-specific pricing strategies and forms local partnerships to penetrate markets, particularly in Asia-Pacific, where growing healthcare infrastructure offers growth potential.

4. What are BMS’s key R&D priorities moving forward?

Focus areas include immuno-oncology, cell and gene therapies, fibrosis, and precision medicine. The emphasis on combination therapies and digital health integration aims to sustain innovation leadership.

5. How does Bristol-Myers Squibb compare to its top competitors?

BMS maintains a specialized focus on immuno-oncology and cell therapies, while competitors like Roche lead in diagnostics and biosimilars, and Merck & Co. has a broader oncology pipeline. BMS’s strategic acquisitions have uniquely strengthened its position in hematology and immunotherapies.


Key Takeaways

  • Bristol-Myers Squibb is a robust player in immuno-oncology, with a diversified pipeline and strategic acquisitions like Celgene underpinning its growth.
  • The company’s revenue is heavily concentrated in oncology, particularly with Opdivo, which surpasses $9 billion annually.
  • BMS faces upcoming patent expirations and biosimilar competition, necessitating pipeline diversification.
  • Strategic focus areas include advancing cell therapies, expanding in emerging markets, and integrating digital innovations.
  • Competition remains fierce, with Roche and Merck leading in biosimilars and broad oncology portfolios, respectively.

Actionable Insights for Stakeholders

  • Investors should monitor pipeline advancements, especially in cell and gene therapy areas, which promise future growth.
  • Business partners can leverage BMS’s focus on immuno-oncology for collaborative development opportunities.
  • Regulators and policymakers should engage with BMS’s innovation strategies, as they drive advances in personalized medicine and oncology care.

References

  1. Bristol-Myers Squibb Annual Report 2022.
  2. IQVIA Institute, "The Global Oncology Market," 2022.
  3. Financial Times, "Top Pharmaceutical Conglomerates," 2022.
  4. Company press releases and clinical trial registries (clinicaltrials.gov).
  5. Market analytics reports, EvaluatePharma, 2022.

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Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.