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mAbxience

Full company profile

uuid0008g9o

Namestring
mAbxience
Legal namestring
MABXIENCE HOLDING SL
Websiteurl
mabxience.com
Company typeenum
Private
Founded yearint
2009
Descriptiontext

mAbxience is a vertically integrated biopharmaceutical company that develops, manufactures, and commercializes biosimilars and provides contract development and manufacturing (CDMO) services to global biopharmaceutical partners. Founded in 2009 and operating as a subsidiary of Fresenius Kabi, the company runs two integrated business lines: an in-house biosimilar development program with current commercial focus on denosumab-based products (Boncresa and Oziltus FDA-approved in the US for osteoporosis and bone cancer indications; Izamby and Denbrayce marketed in 15+ European countries) and an independent CDMO platform offering end-to-end manufacturing services from research batches to commercial scale.

The company's technical platform is anchored in proprietary bioprocess development and manufacturing capabilities, augmented by recent technology partnerships: an AI-driven biomanufacturing optimization initiative with HP Inc. using digital twin technology (announced December 2025) and Genedata Bioprocess, a SaaS-based bioprocess data management platform (implementation announced March 2026). mAbxience has over a decade of experience in the development and commercialization of biopharmaceuticals and holds regulatory clearances across multiple jurisdictions (FDA in the US, CE Mark in Europe).

mAbxience's business model operates through two distinct revenue mechanics. The CDMO arm generates professional services revenue from biopharmaceutical clients requiring contract development and manufacturing. The biosimilar arm operates on a licensing/royalty model where mAbxience handles development and manufacturing while strategic partners — Amneal Pharmaceuticals for the US market (exclusive commercialization rights) and Abbott for emerging markets — commercialize products in their territories. The company serves healthcare providers and patients indirectly through these commercialization partners, with end markets spanning the US, 15+ European countries, and emerging markets. Pricing and contract terms are not publicly disclosed.

Short descriptiontext

mAbxience is a Fresenius Kabi subsidiary that develops and manufactures biosimilars (notably denosumab products for osteoporosis and bone cancer) and provides CDMO services to global biopharmaceutical partners across the US, Europe, and emerging markets.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1,001–5,000
akta.pro rankint
HeadquartersLugano, Switzerland
HQ citystring
Lugano
HQ countrystring
Switzerland
HQ regionstring
Europe
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
biosimilar development, biopharmaceutical manufacturing, CDMO services, biologics contract development, denosumab biosimilars
Industry2 codes
1Monoclonal Antibody (mAb) Biosimilars
CodeHLAAAHAAPrimaryYes
2Contract Development & Manufacturing for Generics (CDMO/CMO)
CodeHLAIABAIPrimaryNo
NAICS code2 codes
  • Biological Product (except Diagnostic) Manufacturing325414
  • Pharmaceutical Preparation Manufacturing325412
SIC code2 codes
  • Biological Products, (No Disgnostic Substances)2836
  • Pharmaceutical Preparations2834
Product category
Biosimilars and Biopharmaceutical CDMO Services
Social media profiles2 records
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model2 records
1CDMO Services
TypeProfessional Services
Description

Contract development and manufacturing organization services providing integrated biopharmaceutical solutions from research batches to commercial batches, both large and small scale.

mabxience.com
2Biosimilar Development and Commercialization
TypeLicensing Royalties
Description

Development and manufacturing of biosimilar products through strategic partnerships, where mAbxience handles development and manufacturing while partners commercialize products in their territories.

prnewswire.co.uk
Marketing channels3 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Personnel, Technology or R&D, Infrastructure, Supply Chain, Operations
GTM typeB2B
B2B
Offering typeServices
Services
Core offering1 text field

mAbxience is a vertically integrated biopharmaceutical company that develops and manufactures biosimilars (notably FDA-approved denosumab biosimilars Boncresa and Oziltus referencing Prolia and XGEVA) and operates an independent CDMO platform providing end-to-end development and manufacturing services from research batches to commercial batches. The company commercializes its biosimilars through strategic partners such as Amneal Pharmaceuticals (US) and Abbott (emerging markets) while offering integrated biopharmaceutical services globally.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 2 values shown
  • FDA approval of two denosumab biosimilars (Boncresa and Oziltus) expanding access to affordable biologic medicines in the United States.
+1 more record
Product overview1 text field

mAbxience is a vertically integrated biopharmaceuticals company specializing in biosimilars and CDMO services. The company operates two core platforms: Biosimilar Development (including Boncresa, Oziltus, Izamby, and Denbrayce denosumab biosimilars) and an independent CDMO platform providing end-to-end manufacturing solutions. The biosimilar portfolio focuses on denosumab-based products for osteoporosis and bone cancer indications, while the CDMO services offer integrated manufacturing from research through commercial scale.

Product and service5 records
1Boncresa (Denosumab Biosimilar)
CategoryBiosimilar
Description

FDA-approved denosumab biosimilar referencing Prolia, developed through partnership with Amneal Pharmaceuticals who holds exclusive US commercialization rights, for the treatment of osteoporosis and bone-related conditions.

2Oziltus (Denosumab Biosimilar)
CategoryBiosimilar
Description

FDA-approved denosumab biosimilar referencing XGEVA, developed through partnership with Amneal Pharmaceuticals who holds exclusive US commercialization rights, for the prevention of skeletal-related events in patients with bone metastases.

3Izamby (Denosumab 60mg Biosimilar)
CategoryBiosimilar
Description

Denosumab 60mg biosimilar approved in European markets for osteoporosis treatment, with patient information materials available in multiple EU countries including Spain, Italy, Croatia, Poland, Denmark, Hungary, Netherlands, Sweden, Romania, Austria, Germany, Norway, UK, and Finland.

4Denbrayce (Denosumab 120mg Biosimilar)
CategoryBiosimilar
Description

Denosumab 120mg biosimilar approved in European markets for bone cancer treatment, with patient reminder cards available in multiple EU countries.

5CDMO Services
CategoryCDMO Platform
Description

Independent Contract Development and Manufacturing Organization (CDMO) platform providing end-to-end integrated biopharmaceutical solutions from research batches to commercial batches, both large and small scale, with over a decade of experience in biopharmaceutical development and commercialization. Serves pharmaceutical companies and biotech firms requiring contract manufacturing services for biologics and biosimilars.

Scale indicator4 records

Each record includes

Type, Value, Description, Source

Partnership4 partners
Strategic tierSupportingTypeTechnology or IntegrationAnnounced on2026-03-10
Description

mAbxience selected Genedata Bioprocess to implement an automated, SaaS-based platform for bioprocess data management across its biopharmaceutical operations. This strategic move aims to improve process efficiency, data integrity, and support future AI-driven process optimization.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-12-22
Description

mAbxience and Amneal announced FDA approval of two denosumab biosimilars (Boncresa referencing Prolia and Oziltus referencing XGEVA). mAbxience handles development and manufacturing while Amneal holds exclusive US commercialization rights. This partnership expanded Amneal's biosimilar portfolio to five commercial products.

Strategic tierCoreTypeTechnology or IntegrationAnnounced on2025-12-03
Description

mAbxience and HP Inc. announced a collaboration to develop an AI solution for optimizing biologic manufacturing processes, including creating a digital twin to improve efficiency and predictability. The project aims to enhance biologics development, operational efficiency, and resource utilization with potential for global replication.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-11-19
Description

Abbott expanded a biosimilar collaboration with mAbxience Holdings S.L. for emerging markets. This collaboration supports Abbott's affordable medicines strategy and expands access to biosimilar treatments in developing regions.

Recent move5 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Biosimilars-focused subsidiary of Samsung Biologics developing and commercializing monoclonal antibody biosimilars (e.g., denosumab, ranibizumab, bevacizumab). Directly comparable to mAbxience as a vertically integrated mAb biosimilar developer with global commercialization partnerships.

TypeDirect peer
Description

Korean biopharmaceutical company that develops, manufactures, and commercializes biosimilars including infliximab, trastuzumab, rituximab, and denosumab biosimilars. Highly comparable in product category (mAb biosimilars), business model (in-house development plus partnered commercialization), and customer base.

TypeDirect peer
Description

Iceland-based biosimilar developer with a portfolio including denosumab biosimilars (referencing Prolia/XGEVA). Direct competitor to mAbxience in the same mAb biosimilar molecules, with comparable vertically integrated development and manufacturing model.

TypeDirect peer
Description

India-headquartered biosimilar business of Biocon Limited, developing and commercializing biosimilars such as trastuzumab, bevacizumab, insulin glargine, and denosumab. Comparable product portfolio, manufacturing scale, and emerging-market commercialization footprint.

TypeDirect peer
Description

European biosimilar developer and manufacturer with a pipeline of biosimilars including ranibizumab, natalizumab, and others. Comparable vertically integrated biosimilar development and CDMO operations, with geographic overlap in European markets.

TypeBroad incumbent
Description

Larger Korean contract development and manufacturing organization (CDMO) for biologics with significant manufacturing capacity and broader client base than mAbxience. Comparable in CDMO capabilities for biopharmaceuticals and in deploying AI/data-driven manufacturing optimization.

TypeBroad incumbent
Description

CDMO arm of Boehringer Ingelheim providing contract development and manufacturing services for biopharmaceuticals and biosimilars. Comparable on the CDMO side, with overlapping capabilities in biologics manufacturing and biosimilar process development.

TypeBroad incumbent
Description

Originator of Prolia/XGEVA (denosumab) and other biologics, also active in biosimilars. Comparable because mAbxience's flagship products directly reference Amgen brands, and Amgen sets the competitive dynamic (defensive pricing, lifecycle management) that will shape mAbxience's US economics.

TypeOthers
Description

Parent company of mAbxience, a global healthcare company providing pharmaceutical and medical device products. Included as the parent rather than a direct competitor; relevant for understanding ownership structure, capital allocation, and strategic priorities constraining or supporting mAbxience.

TypeOthers
Description

Exclusive US commercialization partner for mAbxience's biosimilars and a biosimilar developer in its own right. Comparable as a participant in the same biosimilar value chain, and material to mAbxience's US commercial trajectory though it does not directly compete on manufacturing.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

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Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks7 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers2 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment2 records

Each record includes

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

Ideal customer profile2 records

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
Yes
API detail
Has APIbool
No

Docs URL, Description

Integration2 records

Each record includes

Title, Type, Description, Source

AI capability3 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles4 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&A

Each record includes

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

Investment

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 →

mAbxience

Biosimilars and Biopharmaceutical CDMO Servicesmabxience.com

mAbxience is a Fresenius Kabi subsidiary that develops and manufactures biosimilars (notably denosumab products for osteoporosis and bone cancer) and provides CDMO services to global biopharmaceutical partners across the US, Europe, and emerging markets.

What mAbxience does

mAbxience is a vertically integrated biopharmaceutical company that develops, manufactures, and commercializes biosimilars and provides contract development and manufacturing (CDMO) services to global biopharmaceutical partners. Founded in 2009 and operating as a subsidiary of Fresenius Kabi, the company runs two integrated business lines: an in-house biosimilar development program with current commercial focus on denosumab-based products (Boncresa and Oziltus FDA-approved in the US for osteoporosis and bone cancer indications; Izamby and Denbrayce marketed in 15+ European countries) and an independent CDMO platform offering end-to-end manufacturing services from research batches to commercial scale.

The company's technical platform is anchored in proprietary bioprocess development and manufacturing capabilities, augmented by recent technology partnerships: an AI-driven biomanufacturing optimization initiative with HP Inc. using digital twin technology (announced December 2025) and Genedata Bioprocess, a SaaS-based bioprocess data management platform (implementation announced March 2026). mAbxience has over a decade of experience in the development and commercialization of biopharmaceuticals and holds regulatory clearances across multiple jurisdictions (FDA in the US, CE Mark in Europe).

mAbxience's business model operates through two distinct revenue mechanics. The CDMO arm generates professional services revenue from biopharmaceutical clients requiring contract development and manufacturing. The biosimilar arm operates on a licensing/royalty model where mAbxience handles development and manufacturing while strategic partners — Amneal Pharmaceuticals for the US market (exclusive commercialization rights) and Abbott for emerging markets — commercialize products in their territories. The company serves healthcare providers and patients indirectly through these commercialization partners, with end markets spanning the US, 15+ European countries, and emerging markets. Pricing and contract terms are not publicly disclosed.

mAbxience firmographics

Firmographics
Name
mAbxience
Legal name
MABXIENCE HOLDING SL
Website
https://mabxience.com
Company type
Private
Founded year
2009
Operating status
Operating
Headcount range
1,001–5,000 employees
Short description
mAbxience is a Fresenius Kabi subsidiary that develops and manufactures biosimilars (notably denosumab products for osteoporosis and bone cancer) and provides CDMO services to global biopharmaceutical partners across the US, Europe, and emerging markets.
Ownership category
akta.pro rank

mAbxience industry classification

Industry
Product category
Biosimilars and Biopharmaceutical CDMO Services
NAICS
Biological Product (except Diagnostic) Manufacturing (325414), Pharmaceutical Preparation Manufacturing (325412)
SIC
Biological Products, (No Disgnostic Substances) (2836), Pharmaceutical Preparations (2834)
akta.pro primary industry
Monoclonal Antibody (mAb) Biosimilars (HLAAAHAA)
akta.pro secondary industry
Contract Development & Manufacturing for Generics (CDMO/CMO) (HLAIABAI)

Keywords

  • Biosimilar development
  • Biopharmaceutical manufacturing
  • CDMO services
  • Biologics contract development
  • Denosumab biosimilars

Where mAbxience is headquartered

Location

Headquarters

HQ city
Lugano
HQ country
Switzerland
HQ region
Europe

Offices2 records

Markets served

mAbxience business model

Business model
GTM type
B2B
Offering type
Services
Cost components
Personnel, Technology or R&D, Infrastructure, Supply Chain, Operations

Revenue model

  1. CDMO Services: Contract development and manufacturing organization services providing integrated biopharmaceutical solutions from research batches to commercial batches, both large and small scale.
  2. Biosimilar Development and Commercialization: Development and manufacturing of biosimilar products through strategic partnerships, where mAbxience handles development and manufacturing while partners commercialize products in their territories.

Go-to-market motion2 records

Distribution channels1 record

Marketing channels3 records

mAbxience product offering

Product offering

Core offering

mAbxience is a vertically integrated biopharmaceutical company that develops and manufactures biosimilars (notably FDA-approved denosumab biosimilars Boncresa and Oziltus referencing Prolia and XGEVA) and operates an independent CDMO platform providing end-to-end development and manufacturing services from research batches to commercial batches. The company commercializes its biosimilars through strategic partners such as Amneal Pharmaceuticals (US) and Abbott (emerging markets) while offering integrated biopharmaceutical services globally.

Product overview

mAbxience is a vertically integrated biopharmaceuticals company specializing in biosimilars and CDMO services. The company operates two core platforms: Biosimilar Development (including Boncresa, Oziltus, Izamby, and Denbrayce denosumab biosimilars) and an independent CDMO platform providing end-to-end manufacturing solutions. The biosimilar portfolio focuses on denosumab-based products for osteoporosis and bone cancer indications, while the CDMO services offer integrated manufacturing from research through commercial scale.

Differentiator

Problem solved

Functional benefit

Products and services

  • Boncresa (Denosumab Biosimilar) FDA-approved denosumab biosimilar referencing Prolia, developed through partnership with Amneal Pharmaceuticals who holds exclusive US commercialization rights, for the treatment of osteoporosis and bone-related conditions.
  • Oziltus (Denosumab Biosimilar) FDA-approved denosumab biosimilar referencing XGEVA, developed through partnership with Amneal Pharmaceuticals who holds exclusive US commercialization rights, for the prevention of skeletal-related events in patients with bone metastases.
  • Izamby (Denosumab 60mg Biosimilar) Denosumab 60mg biosimilar approved in European markets for osteoporosis treatment, with patient information materials available in multiple EU countries including Spain, Italy, Croatia, Poland, Denmark, Hungary, Netherlands, Sweden, Romania, Austria, Germany, Norway, UK, and Finland.
  • Denbrayce (Denosumab 120mg Biosimilar) Denosumab 120mg biosimilar approved in European markets for bone cancer treatment, with patient reminder cards available in multiple EU countries.
  • CDMO Services Independent Contract Development and Manufacturing Organization (CDMO) platform providing end-to-end integrated biopharmaceutical solutions from research batches to commercial batches, both large and small scale, with over a decade of experience in biopharmaceutical development and commercialization. Serves pharmaceutical companies and biotech firms requiring contract manufacturing services for biologics and biosimilars.

Quantifiable outcome

  • FDA approval of two denosumab biosimilars (Boncresa and Oziltus) expanding access to affordable biologic medicines in the United States.
  • +1 more outcomes

Companies that use mAbxience

Customer profile

Named customers2 records

Segments2 records

Ideal customer profiles2 records

mAbxience technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Integration2 records

AI capability3 records

Feature3 records

mAbxience partnerships and signals

Strategic signal

Partnerships

Four partnerships are on record, tiered supporting and core.

  • GenedatasupportingTechnology or Integration · 10 March 2026mAbxience selected Genedata Bioprocess to implement an automated, SaaS-based platform for bioprocess data management across its biopharmaceutical operations. This strategic move aims to improve process efficiency, data integrity, and support future AI-driven process optimization.
  • Amneal PharmaceuticalscoreStrategic or Co-development Partner · 22 December 2025mAbxience and Amneal announced FDA approval of two denosumab biosimilars (Boncresa referencing Prolia and Oziltus referencing XGEVA). mAbxience handles development and manufacturing while Amneal holds exclusive US commercialization rights. This partnership expanded Amneal's biosimilar portfolio to five commercial products.
  • HP Inc.coreTechnology or Integration · 3 December 2025mAbxience and HP Inc. announced a collaboration to develop an AI solution for optimizing biologic manufacturing processes, including creating a digital twin to improve efficiency and predictability. The project aims to enhance biologics development, operational efficiency, and resource utilization with potential for global replication.
  • AbbottcoreStrategic or Co-development Partner · 19 November 2025Abbott expanded a biosimilar collaboration with mAbxience Holdings S.L. for emerging markets. This collaboration supports Abbott's affordable medicines strategy and expands access to biosimilar treatments in developing regions.

Scale indicators4 records

Recent moves5 records

Expansion highlights5 records

mAbxience competitors and assessment

Company assessment

Direct peers

  • Samsung Bioepis: Biosimilars-focused subsidiary of Samsung Biologics developing and commercializing monoclonal antibody biosimilars (e.g., denosumab, ranibizumab, bevacizumab). Directly comparable to mAbxience as a vertically integrated mAb biosimilar developer with global commercialization partnerships.
  • Celltrion: Korean biopharmaceutical company that develops, manufactures, and commercializes biosimilars including infliximab, trastuzumab, rituximab, and denosumab biosimilars. Highly comparable in product category (mAb biosimilars), business model (in-house development plus partnered commercialization), and customer base.
  • Alvotech: Iceland-based biosimilar developer with a portfolio including denosumab biosimilars (referencing Prolia/XGEVA). Direct competitor to mAbxience in the same mAb biosimilar molecules, with comparable vertically integrated development and manufacturing model.
  • Biocon Biologics: India-headquartered biosimilar business of Biocon Limited, developing and commercializing biosimilars such as trastuzumab, bevacizumab, insulin glargine, and denosumab. Comparable product portfolio, manufacturing scale, and emerging-market commercialization footprint.
  • Polpharma Biologics: European biosimilar developer and manufacturer with a pipeline of biosimilars including ranibizumab, natalizumab, and others. Comparable vertically integrated biosimilar development and CDMO operations, with geographic overlap in European markets.

Broad incumbents

  • Samsung Biologics: Larger Korean contract development and manufacturing organization (CDMO) for biologics with significant manufacturing capacity and broader client base than mAbxience. Comparable in CDMO capabilities for biopharmaceuticals and in deploying AI/data-driven manufacturing optimization.
  • Boehringer Ingelheim BioXcellence: CDMO arm of Boehringer Ingelheim providing contract development and manufacturing services for biopharmaceuticals and biosimilars. Comparable on the CDMO side, with overlapping capabilities in biologics manufacturing and biosimilar process development.
  • Amgen: Originator of Prolia/XGEVA (denosumab) and other biologics, also active in biosimilars. Comparable because mAbxience's flagship products directly reference Amgen brands, and Amgen sets the competitive dynamic (defensive pricing, lifecycle management) that will shape mAbxience's US economics.

Others

  • Fresenius Kabi: Parent company of mAbxience, a global healthcare company providing pharmaceutical and medical device products. Included as the parent rather than a direct competitor; relevant for understanding ownership structure, capital allocation, and strategic priorities constraining or supporting mAbxience.
  • Amneal Pharmaceuticals: Exclusive US commercialization partner for mAbxience's biosimilars and a biosimilar developer in its own right. Comparable as a participant in the same biosimilar value chain, and material to mAbxience's US commercial trajectory though it does not directly compete on manufacturing.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks7 records

Key highlights7 records

Customer concentration

mAbxience social profiles

Digital presence

mAbxience financial estimates

Financial estimate

Revenue estimate

Valuation estimate

mAbxience leadership team

Management profile

Number of profiles

Profiles4 records

mAbxience funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

mAbxience M&A and investment

M&A and investment

M&A

Investments

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

Frequently asked questions about mAbxience

What does mAbxience do?

mAbxience is a vertically integrated biopharmaceutical company that develops and manufactures biosimilars (notably FDA-approved denosumab biosimilars Boncresa and Oziltus referencing Prolia and XGEVA) and operates an independent CDMO platform providing end-to-end development and manufacturing services from research batches to commercial batches. The company commercializes its biosimilars through strategic partners such as Amneal Pharmaceuticals (US) and Abbott (emerging markets) while offering integrated biopharmaceutical services globally.

Is mAbxience a public or private company?

mAbxience is a private company. It is classified as corporate owned and is currently operating.

When was mAbxience founded?

mAbxience was founded in 2009. It employs 1,001 to 5,000 people.

Where is mAbxience based?

mAbxience is headquartered in Lugano, Switzerland, in the Europe region.

How does mAbxience make money?

Two revenue lines are on record. CDMO Services are the primary driver. The others are biosimilar Development and Commercialization.

Who are mAbxience's main competitors?

Direct peers on record are Samsung Bioepis, Celltrion, Alvotech, Biocon Biologics and Polpharma Biologics. Broad incumbents are Samsung Biologics, Boehringer Ingelheim BioXcellence and Amgen. Others are Fresenius Kabi and Amneal Pharmaceuticals.

Does mAbxience have an API?

No public API is recorded for mAbxience.

What industry is mAbxience in?

mAbxience's product category is Biosimilars and Biopharmaceutical CDMO Services. Its primary akta.pro industry code is HLAAAHAA, Monoclonal Antibody (mAb) Biosimilars, with a secondary code of HLAIABAI, Contract Development & Manufacturing for Generics (CDMO/CMO). Its NAICS code is 325414 and its SIC code is 2836.

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Live signals
FinanzNachrichten.deEQS-News: mAbxience: Fresenius schließt die Übernahme von mAbxience ab und schafft damit eine stärkere Plattform für den künftigen Ausbau des PortfoliosFresenius completed its acquisition of the remaining 45% of mAbxience from Insud Pharma, achieving full ownership. The deal builds on a 2022 partnership and places mAbxience's biosimilar platform under Fresenius Kabi's biopharma business. The company will continue supporting existing customers and maintaining quality and supply.AktienFresenius schließt die Übernahme von mAbxience ab und schafft damit eine stärkere Plattform für den künftigen Ausbau des PortfoliosFresenius acquired the remaining 45% of mAbxience from Insud Pharma, completing its ownership. The deal builds on a 2022 partnership and places mAbxience's biosimilar platform fully under Fresenius Kabi's biopharma business. It aims to improve quality, supply security, and patient access to biosimilars.AdvfnFresenius completes acquisition of mAbxience, creating a stronger platform for future portfolio expansionFresenius completed its acquisition of the remaining 45% of mAbxience from Insud Pharma, bringing the biosimilars platform under full ownership within Fresenius Kabi's Biopharma business. The deal builds on a 2022 partnership and aims to enhance quality, supply resilience, and patient access as biologics lose exclusivity.InvestorsinhealthcareSpain: Fresenius acquires remaining 45% of mAbxience for up to €750mFresenius acquired the remaining 45% of mAbxience from Insud Pharma and Invim Corporativo for up to €750m, including a €50m contingent payment. The deal builds on a 2022 partnership and creates a wholly owned biopharma business. mAbxience generated over €320m in 2025 revenue.PR NewswireFresenius completes acquisition of mAbxience, creating a stronger platform for future portfolio expansionFresenius completed its acquisition of the remaining 45% of mAbxience from Insud Pharma, making the biosimilars platform wholly owned within Fresenius Kabi's Biopharma business. The deal builds on a 2022 partnership and aims to enhance quality, supply resilience, and patient access to biosimilars as biologics lose exclusivity.MorningstarFresenius completes acquisition of mAbxience, creating a stronger platform for future portfolio expansionFresenius completed its acquisition of mAbxience, acquiring the remaining 45% from Insud Pharma to make the biosimilars platform wholly owned. The deal builds on a 2022 partnership and aims to enhance quality, supply resilience, and patient access to biosimilars as biologics lose exclusivity.YahooSandoz and mAbxience agree on emicizumab biosimilar partnershipSandoz and mAbxience signed a licensing, development, manufacturing and commercialisation agreement for an emicizumab biosimilar for haemophilia A. mAbxience will develop and manufacture at its GMP facilities in Argentina and Spain, while Sandoz gets exclusive global commercialisation rights excluding Argentina, Paraguay and Uruguay. The reference medicine Hemlibra has estimated global sales of $5.7bn.Pharmaceutical TechnologySandoz and mAbxience agree on emicizumab biosimilar partnershipSandoz and mAbxience signed a licensing, development, manufacturing and commercialisation agreement for an emicizumab biosimilar for haemophilia A. The candidate is in early-stage development, referencing Hemlibra with estimated global sales of $5.7bn. mAbxience will manufacture at its GMP facilities in Argentina and Spain, while Sandoz holds exclusive global commercialisation rights.FinanzNachrichten.deEQS-News: mAbxience und Sandoz unterzeichnen Kooperationsvereinbarung zur weltweiten Förderung des Zugangs zu BiosimilarsmAbxience and Sandoz signed a licensing, development, manufacturing, and marketing agreement for an Emicizumab biosimilar candidate. mAbxience will handle development and manufacturing in Spain and Argentina, while Sandoz holds global exclusive marketing rights except in Argentina, Uruguay, and Paraguay. The agreement aims to expand patient access to the biosimilar, which targets a global reference market of about $5.7 billion.Drug Store NewsSandoz inks agreement with mAbxience for Hemlibra biosimilarSandoz announced a licensing, development, manufacturing and commercialization agreement with mAbxience for a proposed emicizumab biosimilar, the first hemophilia biosimilar in its pipeline. The reference medicine Hemlibra has an estimated $5.7 billion global market. The collaboration aims to broaden patient access to biosimilar medicines worldwide.