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Celgene

Full company profile

uuid0007525

Namestring
Celgene
Legal namestring
Celgene Corporation
Websiteurl
celgene.com
Company typeenum
Private
Founded yearint
1986
Descriptiontext

Celgene Corporation was a Summit, New Jersey-based biopharmaceutical company founded in 1986 that developed and commercialized therapies for cancer and immune-inflammatory diseases, with a concentration in hematologic malignancies. The company's core commercial franchise centered on three proprietary drugs: Revlimid (lenalidomide), Pomalyst (pomalidomide), and Thalomid (thalidomide), all used in the treatment of multiple myeloma and related blood cancers. Revlimid, launched in 2005, grew into one of the world's best-selling cancer drugs, reaching $8.1B in annual revenue by 2017 and accumulating over $21B in cumulative net earnings through 2025. Celgene also built a pipeline extension platform known as CELMoD (Celgene Modulatory Drug), with candidates like mezigdomide and iberdomide designed to defend the multiple myeloma franchise, and expanded into cell therapy through its $9B acquisition of Juno Therapeutics in 2018.

Celgene operated a traditional branded pharmaceutical revenue model, monetizing proprietary drugs through specialty distribution channels, primarily in the U.S. (where Revlimid was priced near $1,000 per pill) and select international markets. The company systematically layered New Chemical Entity (NCE) and Orphan Drug Exclusivity to extend Revlimid's franchise longevity. To diversify beyond Revlimid and prepare for its eventual loss of exclusivity, Celgene executed an aggressive M&A strategy spanning 2010-2018, including Juno Therapeutics ($9B), Receptos ($7.32B), EngMab ($600M), Quanticel ($485M), and over a dozen additional transactions, adding capabilities in CAR-T cell therapy, immunology (ozanimod), and myelofibrosis (fedratinib). Celgene's customer base was fragmented across hematology-oncology prescribers and patients with multiple myeloma, myelodysplastic syndromes, and related conditions. In 2019, Bristol Myers Squibb acquired Celgene for $74 billion in one of the largest pharmaceutical mergers in history, integrating Celgene's assets into BMS's oncology franchise and ending Celgene's standalone operating existence.

Short descriptiontext

Celgene Corporation was a Summit, NJ-based biopharmaceutical company (founded 1986) that developed and commercialized branded oncology and immunology therapies, anchored by the multiple myeloma drug Revlimid, until its $74B acquisition by Bristol Myers Squibb in 2019.

Operating statusenum
Acquired
Ownership categoryenum
Headcount rangeband
5,001–10,000
akta.pro rankint
HeadquartersSummit, United States
HQ citystring
Summit
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Keyword5 values
oncology pharmaceutical drugs, multiple myeloma treatment, hematology biopharmaceuticals, immunomodulatory drug therapy, cancer drug development
Industry2 codes
1Dendritic Cell & Other APC-based Therapies
CodeHLAAABAFPrimaryYes
2Personalized Therapeutic Design (neoantigen vaccines, individualized cell/gene therapies)
CodeHLAAANAKPrimaryNo
NAICS code2 codes
  • Pharmaceutical Preparation Manufacturing325412
  • Biological Product (except Diagnostic) Manufacturing325414
SIC code2 codes
  • Pharmaceutical Preparations2834
  • Biological Products, (No Disgnostic Substances)2836
Product category
Oncology / Hematology Pharmaceuticals
Social media profiles2 records
Revenue model1 record
1Pharmaceutical drug sales
TypeOne Time License
Description

Celgene generated revenue through the sale of proprietary pharmaceutical drugs, primarily in the oncology and hematology therapeutic areas. Key products included Revlimid (lenalidomide), Thalomid (thalidomide), and Pomalyst (pomalidomide).

drugpatentwatch.com
Cost components5 values
Technology or R&D, Marketing or Sales, Personnel, Supply Chain, Operations
Pricing details1 tier
1Revlimid (lenalidomide) - approximately $1,000 per pill in the U.S.
ModelOtherBilling cadenceOther
Notes

At nearly $1,000 per pill in the U.S., compared to prices two-thirds lower in some European countries.

propublica.org
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Celgene was a biopharmaceutical company that discovered, developed, and commercialized innovative therapies to treat cancer and immune-inflammatory-related diseases. Its flagship products were oral immunomodulatory drugs — Revlimid (lenalidomide), Pomalyst (pomalidomide), and Thalomid (thalidomide) — primarily for multiple myeloma and myelodysplastic syndromes. The company operated proprietary R&D platforms including the CELMoD drug development platform and cell therapy capabilities.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 value
  • Reduced risk of progression or death by 52% in relapsed or refractory multiple myeloma patients with mezigdomide (a CELMoD class drug building on Revlimid franchise)
Product overview1 text field

Celgene Corporation was a biopharmaceutical company that developed drugs for cancer and inflammatory diseases. Its core products included Revlimid, Pomalyst, and Thalomid for multiple myeloma treatment. The company was acquired by Bristol Myers Squibb in 2019 for $74 billion. The products operated independently as branded pharmaceuticals rather than as a unified software platform with modules.

Product and service4 records
1Revlimid (lenalidomide)
CategoryOncology / Hematology Pharmaceutical
Description

Oral immunomodulatory cancer drug for the treatment of multiple myeloma and other hematologic malignancies. Generated $8.1 billion in annual revenue by 2017.

2Pomalyst (pomalidomide)
CategoryOncology / Hematology Pharmaceutical
Description

Oral immunomodulatory drug for the treatment of multiple myeloma, part of the Revlimid/Pomalyst franchise.

3Thalomid (thalidomide)
CategoryOncology / Hematology Pharmaceutical
Description

Oral immunomodulatory drug for the treatment of multiple myeloma that Celgene systematically escalated in price over time.

4Abecma (idecabtagene vicleucel)
CategoryCell Therapy / Oncology Pharmaceutical
Description

CAR-T cell therapy for multiple myeloma, developed by Celgene and brought to market following Bristol Myers Squibb's 2019 acquisition.

Scale indicator4 records

Each record includes

Type, Value, Description, Source

Partnership1 partner
1Celgene
Strategic tierMinorTypeOthersAnnounced on2012-01-01
Description

DeuteRx (formerly Deuteria Pharmaceuticals) was acquired by Celgene in 2012. The transaction involved Deuteria Pharmaceuticals and selected oncology programs, representing one of DeuteRx's four completed M&A transactions over its history. The deal was part of DeuteRx's strategic exit from metabolic, cancer, and psychiatric disorders programs to larger pharmaceutical companies.

nationaltoday.com
Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Acquired Celgene for $74B in 2019 and now owns the entire Celgene franchise including Revlimid, Pomalyst, Abecma, and the CELMoD platform. Operates the same oncology/hematology business that Celgene built and is the closest comparable peer.

TypeDirect peer
Description

Large biotechnology company with a significant oncology and hematology franchise including Kyprolis (carfilzomib) for multiple myeloma, directly competing with Celgene's myeloma portfolio.

TypeDirect peer
Description

Major oncology player with CAR-T therapies via Kite Pharma (Tecartus, Yescarta), directly comparable to Celgene's Juno-derived Abecma cell therapy franchise.

TypeDirect peer
Description

Global pharmaceutical company with a substantial oncology and hematology franchise, including Kymriah (the first FDA-approved CAR-T therapy), directly competing with Celgene's multiple myeloma and cell therapy assets.

TypeDirect peer
Description

Major oncology competitor with Darzalex (daratumumab) for multiple myeloma and Carvykti CAR-T therapy, directly competing with Celgene's Revlimid franchise and Juno-derived cell therapy assets.

TypeDirect peer
Description

Acquired Celgene competitor Pharmacyclics and markets Imbruvica (ibrutinib) and Venclexta (venetoclax) for hematologic malignancies, overlapping with Celgene's hematology franchise.

TypeBroad incumbent
Description

Global biopharmaceutical company with a rapidly expanding oncology franchise (Tagrisso, Imfinzi, Calquence, Enhertu) that competes across multiple cancer indications overlapping with Celgene's oncology portfolio.

TypeBroad incumbent
Description

Global pharmaceutical incumbent with a broad oncology portfolio including multiple myeloma therapies and biologics, providing overlapping competition with Celgene's hematology franchise.

TypeBroad incumbent
Description

Global pharmaceutical leader with deep oncology and hematology franchises, including biologics and targeted therapies that overlap with Celgene's therapeutic focus areas.

TypeBroad incumbent
Description

Global pharmaceutical incumbent anchored by Keytruda in oncology; broad portfolio and pipeline overlap with Celgene's oncology development programs.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights5 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment2 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile1 record

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles9 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A15 records

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment67 records

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Celgene

Oncology / Hematology Pharmaceuticalscelgene.com

Celgene Corporation was a Summit, NJ-based biopharmaceutical company (founded 1986) that developed and commercialized branded oncology and immunology therapies, anchored by the multiple myeloma drug Revlimid, until its $74B acquisition by Bristol Myers Squibb in 2019.

What Celgene does

Celgene Corporation was a Summit, New Jersey-based biopharmaceutical company founded in 1986 that developed and commercialized therapies for cancer and immune-inflammatory diseases, with a concentration in hematologic malignancies. The company's core commercial franchise centered on three proprietary drugs: Revlimid (lenalidomide), Pomalyst (pomalidomide), and Thalomid (thalidomide), all used in the treatment of multiple myeloma and related blood cancers. Revlimid, launched in 2005, grew into one of the world's best-selling cancer drugs, reaching $8.1B in annual revenue by 2017 and accumulating over $21B in cumulative net earnings through 2025. Celgene also built a pipeline extension platform known as CELMoD (Celgene Modulatory Drug), with candidates like mezigdomide and iberdomide designed to defend the multiple myeloma franchise, and expanded into cell therapy through its $9B acquisition of Juno Therapeutics in 2018.

Celgene operated a traditional branded pharmaceutical revenue model, monetizing proprietary drugs through specialty distribution channels, primarily in the U.S. (where Revlimid was priced near $1,000 per pill) and select international markets. The company systematically layered New Chemical Entity (NCE) and Orphan Drug Exclusivity to extend Revlimid's franchise longevity. To diversify beyond Revlimid and prepare for its eventual loss of exclusivity, Celgene executed an aggressive M&A strategy spanning 2010-2018, including Juno Therapeutics ($9B), Receptos ($7.32B), EngMab ($600M), Quanticel ($485M), and over a dozen additional transactions, adding capabilities in CAR-T cell therapy, immunology (ozanimod), and myelofibrosis (fedratinib). Celgene's customer base was fragmented across hematology-oncology prescribers and patients with multiple myeloma, myelodysplastic syndromes, and related conditions. In 2019, Bristol Myers Squibb acquired Celgene for $74 billion in one of the largest pharmaceutical mergers in history, integrating Celgene's assets into BMS's oncology franchise and ending Celgene's standalone operating existence.

Celgene firmographics

Firmographics
Name
Celgene
Legal name
Celgene Corporation
Website
https://celgene.com
Company type
Private
Founded year
1986
Operating status
Acquired
Headcount range
5,001–10,000 employees
Short description
Celgene Corporation was a Summit, NJ-based biopharmaceutical company (founded 1986) that developed and commercialized branded oncology and immunology therapies, anchored by the multiple myeloma drug Revlimid, until its $74B acquisition by Bristol Myers Squibb in 2019.
Ownership category
akta.pro rank

Celgene industry classification

Industry
Product category
Oncology / Hematology Pharmaceuticals
NAICS
Pharmaceutical Preparation Manufacturing (325412), Biological Product (except Diagnostic) Manufacturing (325414)
SIC
Pharmaceutical Preparations (2834), Biological Products, (No Disgnostic Substances) (2836)
akta.pro primary industry
Dendritic Cell & Other APC-based Therapies (HLAAABAF)
akta.pro secondary industry
Personalized Therapeutic Design (neoantigen vaccines, individualized cell/gene therapies) (HLAAANAK)

Keywords

  • Oncology pharmaceutical drugs
  • Multiple myeloma treatment
  • Hematology biopharmaceuticals
  • Immunomodulatory drug therapy
  • Cancer drug development

Where Celgene is headquartered

Location

Headquarters

HQ city
Summit
HQ country
United States
HQ region
North America

Markets served

Celgene business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Marketing or Sales, Personnel, Supply Chain, Operations

Revenue model

  1. Pharmaceutical drug sales: Celgene generated revenue through the sale of proprietary pharmaceutical drugs, primarily in the oncology and hematology therapeutic areas. Key products included Revlimid (lenalidomide), Thalomid (thalidomide), and Pomalyst (pomalidomide).

Pricing tiers

ModelBillingPrice
OtherOtherRevlimid (lenalidomide) - approximately $1,000 per pill in the U.S.

Celgene product offering

Product offering

Core offering

Celgene was a biopharmaceutical company that discovered, developed, and commercialized innovative therapies to treat cancer and immune-inflammatory-related diseases. Its flagship products were oral immunomodulatory drugs — Revlimid (lenalidomide), Pomalyst (pomalidomide), and Thalomid (thalidomide) — primarily for multiple myeloma and myelodysplastic syndromes. The company operated proprietary R&D platforms including the CELMoD drug development platform and cell therapy capabilities.

Product overview

Celgene Corporation was a biopharmaceutical company that developed drugs for cancer and inflammatory diseases. Its core products included Revlimid, Pomalyst, and Thalomid for multiple myeloma treatment. The company was acquired by Bristol Myers Squibb in 2019 for $74 billion. The products operated independently as branded pharmaceuticals rather than as a unified software platform with modules.

Differentiator

Problem solved

Functional benefit

Products and services

  • Revlimid (lenalidomide) Oral immunomodulatory cancer drug for the treatment of multiple myeloma and other hematologic malignancies. Generated $8.1 billion in annual revenue by 2017.
  • Pomalyst (pomalidomide) Oral immunomodulatory drug for the treatment of multiple myeloma, part of the Revlimid/Pomalyst franchise.
  • Thalomid (thalidomide) Oral immunomodulatory drug for the treatment of multiple myeloma that Celgene systematically escalated in price over time.
  • Abecma (idecabtagene vicleucel) CAR-T cell therapy for multiple myeloma, developed by Celgene and brought to market following Bristol Myers Squibb's 2019 acquisition.

Quantifiable outcome

  • Reduced risk of progression or death by 52% in relapsed or refractory multiple myeloma patients with mezigdomide (a CELMoD class drug building on Revlimid franchise)

Companies that use Celgene

Customer profile

Segments2 records

Ideal customer profiles1 record

Celgene technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Celgene partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • CelgeneminorOthers · 1 January 2012DeuteRx (formerly Deuteria Pharmaceuticals) was acquired by Celgene in 2012. The transaction involved Deuteria Pharmaceuticals and selected oncology programs, representing one of DeuteRx's four completed M&A transactions over its history. The deal was part of DeuteRx's strategic exit from metabolic, cancer, and psychiatric disorders programs to larger pharmaceutical companies.

Scale indicators4 records

Recent moves6 records

Expansion highlights5 records

Celgene competitors and assessment

Company assessment

Direct peers

  • Bristol Myers Squibb: Acquired Celgene for $74B in 2019 and now owns the entire Celgene franchise including Revlimid, Pomalyst, Abecma, and the CELMoD platform. Operates the same oncology/hematology business that Celgene built and is the closest comparable peer.
  • Amgen: Large biotechnology company with a significant oncology and hematology franchise including Kyprolis (carfilzomib) for multiple myeloma, directly competing with Celgene's myeloma portfolio.
  • Gilead Sciences: Major oncology player with CAR-T therapies via Kite Pharma (Tecartus, Yescarta), directly comparable to Celgene's Juno-derived Abecma cell therapy franchise.
  • Novartis: Global pharmaceutical company with a substantial oncology and hematology franchise, including Kymriah (the first FDA-approved CAR-T therapy), directly competing with Celgene's multiple myeloma and cell therapy assets.
  • Johnson & Johnson: Major oncology competitor with Darzalex (daratumumab) for multiple myeloma and Carvykti CAR-T therapy, directly competing with Celgene's Revlimid franchise and Juno-derived cell therapy assets.
  • AbbVie: Acquired Celgene competitor Pharmacyclics and markets Imbruvica (ibrutinib) and Venclexta (venetoclax) for hematologic malignancies, overlapping with Celgene's hematology franchise.

Broad incumbents

  • AstraZeneca: Global biopharmaceutical company with a rapidly expanding oncology franchise (Tagrisso, Imfinzi, Calquence, Enhertu) that competes across multiple cancer indications overlapping with Celgene's oncology portfolio.
  • Pfizer: Global pharmaceutical incumbent with a broad oncology portfolio including multiple myeloma therapies and biologics, providing overlapping competition with Celgene's hematology franchise.
  • Roche: Global pharmaceutical leader with deep oncology and hematology franchises, including biologics and targeted therapies that overlap with Celgene's therapeutic focus areas.
  • Merck & Co. Global pharmaceutical incumbent anchored by Keytruda in oncology; broad portfolio and pipeline overlap with Celgene's oncology development programs.

Market position

Strengths4 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights5 records

Customer concentration

Celgene social profiles

Digital presence

Celgene financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Celgene leadership team

Management profile

Number of profiles

Profiles9 records

Celgene funding detail

Funding detail

Funding overview

Funding rounds

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Celgene M&A and investment

M&A and investment

M&A15 records

Investments67 records

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Celgene

What does Celgene do?

Celgene was a biopharmaceutical company that discovered, developed, and commercialized innovative therapies to treat cancer and immune-inflammatory-related diseases. Its flagship products were oral immunomodulatory drugs — Revlimid (lenalidomide), Pomalyst (pomalidomide), and Thalomid (thalidomide) — primarily for multiple myeloma and myelodysplastic syndromes. The company operated proprietary R&D platforms including the CELMoD drug development platform and cell therapy capabilities.

Is Celgene a public or private company?

Celgene is a private company. It is classified as corporate owned and is currently acquired.

When was Celgene founded?

Celgene was founded in 1986. It employs 5,001 to 10,000 people.

Where is Celgene based?

Celgene is headquartered in Summit, United States, in the North America region.

How does Celgene make money?

One revenue line is on record: pharmaceutical drug sales.

Who are Celgene's main competitors?

Direct peers on record are Bristol Myers Squibb, Amgen, Gilead Sciences, Novartis, Johnson & Johnson and AbbVie. Broad incumbents are AstraZeneca, Pfizer, Roche and Merck & Co..

Does Celgene have an API?

No public API is recorded for Celgene.

What industry is Celgene in?

Celgene's product category is Oncology / Hematology Pharmaceuticals. Its primary akta.pro industry code is HLAAABAF, Dendritic Cell & Other APC-based Therapies, with a secondary code of HLAAANAK, Personalized Therapeutic Design (neoantigen vaccines, individualized cell/gene therapies). Its NAICS code is 325412 and its SIC code is 2834.

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Live signals
DrugPatentWatchStop Tracking Drug Patents. Start Tracking Who Controls Them.Purdue Pharma dissolved on May 1, 2026, with its OxyContin patents now held by Knoa Pharma, a nonprofit-owned successor. The article argues patent databases miss control changes like M&A carve-outs, bankruptcy, and royalty monetization, citing five cases including Bristol Myers Squibb's $74B Celgene deal and Allergan's tribe transfer.BioSpaceBMS’ neuro renaissance was built on back of Celgene mega-mergerBristol Myers Squibb is building its neuroscience pipeline on the 2019 Celgene merger, with Cobenfy readouts for Alzheimer's psychosis delayed to 2027. The company also has assets like irafamdastat and moponetug in development, and a continuum-of-care strategy targeting both disease-modifying and symptomatic treatments.DrugPatentWatchThe Myth of the Stable Drug Patent: Why IPRs Change the Game OvernightThe article details how the U.S. Patent and Trademark Office (USPTO) reversed its inter partes review (IPR) policies in 2025 and 2026, centralizing institution decisions under the Director and causing a 43% drop in petition acceptance rates. It contrasts this recent regulatory shift with historical data showing IPRs significantly reduced branded drug revenues by a median of 79% after patent invalidation between 2012 and 2021. The piece also highlights specific corporate impacts, including stock volatility for Acorda Therapeutics and legal battles involving Celgene over Revlimid patents.DrugPatentWatchThe Safe Patent Portfolio Trap: Why Minimal Filing Costs Pharma a Decade of GrowthThe article analyzes how pharmaceutical companies like AbbVie, Celgene, and Amgen used complex patent strategies to extend market exclusivity for blockbuster drugs, contrasting this with Pfizer's experience where generic entry caused immediate revenue loss. It highlights that while aggressive patenting can delay competition by years, regulators are increasingly challenging these practices as 'junk patents,' leading to delistings and antitrust scrutiny.BioWorldCourt clears path for suit claiming BMS delayed drug approvalA trustee suit claims Bristol Myers Squibb delayed FDA approval of Breyanzi, a gene therapy for non-Hodgkin lymphoma, to avoid milestone payments from its 2019 $74 billion Celgene acquisition. The court has cleared the path for the suit.BioPharma DiveBristol Myers wins ‘milestone’ FDA approval of myeloma drug acquired from CelgeneThe FDA granted accelerated approval to Bristol Myers Squibb's Zenbexus for the second-line treatment of multiple myeloma, aiming to sustain the company's franchise amid declining sales from generic competition. Clinical data showed the drug achieved minimal residual disease-negative status in 41% of patients, significantly outperforming the comparator regimen, which supports potential full approval pending further survival results. Bristol Myers expects significant market uptake as many patients have not been previously exposed to competitor Johnson & Johnson’s Darzalex.STATPharmalittle: We're reading about a lawsuit over lab tests for meds, a Bristol myeloma drug, and moreThe U.S. Food and Drug Administration approved Bristol Myers Squibb's Zenbexus, the first drug in a new class called CELMoDs for treating advanced multiple myeloma. Simultaneously, a U.S. appeals court ruled that UMB Bank can represent former Celgene shareholders in a $6.7 billion lawsuit alleging Bristol Myers Squibb delayed regulatory approvals to avoid paying contingent value rights following its 2019 acquisition of Celgene.FiercePharmaIt's BMS vs. Celgene investors once more after US appeals court revives lawsuitA U.S. federal appeals court has reinstated a lawsuit filed by Celgene shareholders against Bristol Myers Squibb, alleging that BMS intentionally delayed the FDA approval of the drug Breyanzi to avoid paying over $6 billion in contingent value rights. The ruling overturned a previous dismissal regarding the trustee's jurisdiction, allowing the breach-of-contract claims to proceed after the court determined all parties accepted the current trustee's appointment. This legal battle stems from BMS's 2019 acquisition of Celgene, where specific drug approvals triggered financial payouts that were missed due to the delayed authorization of Breyanzi.pharmaphorumBMS bags first approval for myeloma CELMoD ZenbexusBristol Myers Squibb received accelerated approval for iberdomide (Zenbexus) as a second-line therapy for multiple myeloma, combined with daratumumab and dexamethasone. The approval is based on the EXCALIBER-RRMM study, which showed a 41% MRD-negative response rate versus 21% in the control arm. Full approval depends on confirmatory trials, and a $6.7B shareholder lawsuit has been revived.ReutersLawsuit against Bristol Myers over delayed cancer drug is revivedA U.S. federal appeals court revived a $6.7 billion lawsuit accusing Bristol Myers Squibb of delaying FDA approvals for three drugs to avoid paying contingent value rights to former Celgene shareholders. The 2nd Circuit Court ruled that UMB Bank had standing to represent the shareholders, overturning a previous dismissal by a district judge. The case centers on allegations that Bristol Myers slow-walked the approval process for drugs including Breyanzi to circumvent contractual payout obligations tied to its $80.3 billion acquisition of Celgene.