Developer docs
API playgroundTry for free, no card

Search company profiles

Norgine

Full company profile

uuid0006qdz

Namestring
Norgine
Legal namestring
Norgine B.V.
Websiteurl
norgine.com
Company typeenum
Private
Founded yearint
1906
Descriptiontext

Norgine is a European specialist pharmaceutical company founded in 1906 and headquartered in Amsterdam, Netherlands, with a direct commercial presence spanning all major European markets plus Australia and New Zealand. The company develops, in-licenses, manufactures, and commercializes prescription medicines across four therapeutic areas: gastroenterology (e.g., MOVICOL for constipation, MOVIPREP and PLENVU for bowel preparation prior to colonoscopy), hepatology (XIFAXAN/TARGAXAN for hepatic encephalopathy; in-licensed hepatitis delta combination with Vir Biotechnology), rare diseases (XOLREMDI for WHIM syndrome, PEDMARQSI for cisplatin-induced ototoxicity in pediatric patients, IFINWIL for high-risk neuroblastoma), and oncology supportive care and diagnostics (LYMPHOSEEK for sentinel lymph node biopsy, ENDOCUFF VISION colonoscopy device). Manufacturing is owned and operated from Hengoed, Wales (over 600 employees, approximately 50 million packs produced annually, modernized high-speed lines powered by 100% low-carbon electricity) and Dreux, France, providing supply resilience and quality control across the proprietary and select in-licensed portfolio.

The business model combines direct product sales (over €500M annual net product sales per company website, with total enterprise revenue approximately $650M per February 2026 disclosure) with licensing income, milestone payments, and royalties from partners. Revenue is generated primarily through field sales to gastroenterology, hepatology, rare disease, and oncology specialists, and through direct supply to national healthcare systems including NHS England (which funds ENDOCUFF VISION via the Innovation Technology Payment for bowel cancer screening). Growth is driven by a hybrid strategy of in-licensing and acquisitions: notable transactions include the Merus Labs acquisition in 2017 for C$342 million (adding 12 established brands including SINTROM, EMSELEX, ELANTAN, ISOKET, DEPONIT, SALAGEN, ESTRADERM, VANCOCIN), the Azanta acquisition in 2020, and the Theravia acquisition completed in August 2025 for rare disease depth, alongside licensing partnerships with X4 Pharmaceuticals (XOLREMDI), Navidea (LYMPHOSEEK), and Alfasigma (XIFAXAN/TARGAXAN). Norgine Ventures, established in 2012, provides complementary debt-like financing to innovative healthcare companies, creating a deal-flow pipeline across Europe and the US.

The company is privately held and primarily controlled by principal shareholder Peter Stein (Executive Chairman and former CEO), with institutional investment from Goldman Sachs Asset Management commencing in 2022. Leadership includes CEO Janneke van der Kamp (appointed October 2024), Chief Operating Officer Saulo Martiniano, Chief Development and Medical Officer Dr Alastair Benbow, and other regional general managers across DACH and the Netherlands. Customers include national healthcare systems across Europe and Australasia, with no single customer accounting for a dominant share of revenue; the company reports serving approximately 25 million patients annually across its portfolio. Strategic execution is supported by multiple recent regulatory wins including EU, Swissmedic, and Australian approvals for PEDMARQSI and the first-in-EU authorization of XOLREMDI under exceptional circumstances for the ultra-rare WHIM syndrome indication.

Short descriptiontext

Norgine is a privately held European specialty pharmaceutical company founded in 1906 and headquartered in Amsterdam, directly commercializing gastroenterology, hepatology, rare disease, and oncology supportive-care medicines across Europe, Australia, and New Zealand through owned manufacturing (Wales and France) and a hybrid in-licensing and acquisition growth model.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1,001–5,000
akta.pro rankint
HeadquartersAmsterdam, Netherlands
HQ citystring
Amsterdam
HQ countrystring
Netherlands
HQ regionstring
Europe
Markets served

Serves global market

Offices5 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
specialty pharmaceuticals, gastroenterology medicines, rare disease therapeutics, bowel preparation products, hepatic encephalopathy treatments
Industry3 codes
1Primary Care & General Medicine Pharmaceuticals
CodeHLAIAAAAPrimaryYes
2Generic Finished Dosage Form (FDF) Manufacturing
CodeHLAIABAHPrimaryNo
3Infectious Disease Specialty Pharmaceuticals (Non-vaccine)
CodeHLAIACAMPrimaryNo
NAICS code3 codes
  • Pharmaceutical Preparation Manufacturing325412
  • Pharmaceutical and Medicine Manufacturing3254
  • Pharmaceutical and Medicine Manufacturing32541
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Specialty Pharmaceuticals
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model4 records
1Net Product Sales
TypeOne Time License
Description

Direct sales of pharmaceutical products through Norgine's commercial infrastructure across Europe, Australia, and New Zealand. Products include MOVICOL, MOVIPREP, PLENVU, XIFAXAN/TARGAXAN, and others. Reported over €500 million in net product sales.

norgine.com
2Licensing Revenue
TypeLicensing Royalties
Description

Norgine receives licensing fees and milestone payments from partners for commercialization rights in licensed territories. Also receives royalties on product sales.

prnewswire.com
3Manufacturing Services
TypeHardware Sales
Description

Manufacturing pharmaceutical products for both proprietary portfolio and selected in-licensing partners. Operations at Hengoed, Wales and Dreux, France sites producing approximately 50 million packs annually.

norgine.com
4Strategic Investments
TypeManaged Services
Description

Norgine received £67 million strategic investment including £23 million from UK Government's Life Sciences Innovative Manufacturing Fund for Hengoed facility expansion.

pharmtech.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels4 records

Each record includes

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

Cost components6 values
Personnel, Operations, Marketing or Sales, Technology or R&D, Supply Chain, Others
Pricing details1 tier
1XOLREMDI for WHIM syndrome - premium rare disease pricing
ModelOtherBilling cadenceOther
Notes

As a treatment for ultra-rare WHIM syndrome approved under exceptional circumstances, XOLREMDI commands premium pricing typical of orphan drugs. Specific pricing not publicly disclosed.

prnewswire.com
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 2 records shown
1Norgine Ventures
Description

Complementary business established in 2012 supporting innovative healthcare companies through debt-like financing in Europe and the US

norgine.com
+1 more record
Core offering1 text field

Norgine is a European specialist pharmaceutical company that develops, manufactures, and commercializes prescription medicines across gastroenterology, hepatology, rare diseases, and oncology supportive care. The company operates its own manufacturing facilities in Hengoed, Wales and Dreux, France, producing approximately 50 million packs of medicines and medical devices annually, and commercializes a portfolio that includes in-licensed and proprietary products across all major European markets, Australia, and New Zealand.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 6 values shown
  • 88% undetectable viral response at 96 weeks in Phase 2 hepatitis delta combination regimen (Vir Biotechnology data)
+5 more records
Product overview1 text field

Norgine is a leading European specialty pharmaceutical company offering a diversified portfolio of products across gastroenterology, hepatology, oncology supportive care, and rare diseases. The core portfolio includes MOVICOL® (constipation treatment), MOVIPREP® and PLENVU® (bowel preparations for colonoscopy), XIFAXAN®/TARGAXAN® (hepatic encephalopathy treatment), LYMPHOSEEK® (sentinel lymph node diagnostic), ENDOCUFF VISION® (colonoscopy device), PEDMARQSI® (pediatric ototoxicity prevention), XOLREMDI® (WHIM syndrome treatment), and IFINWIL® (neuroblastoma treatment). The company operates through direct commercialization in Europe and Australia with over €500 million in net product sales.

Product and service14 records
1MOVICOL
CategoryGastroenterology
Description

Leading anti-constipation treatment for chronic constipation, sold primarily in European markets and Australia.

2MOVIPREP
CategoryGastroenterology
Description

Two-litre PEG-based bowel preparation for adults prior to colonoscopy procedures.

3PLENVU
CategoryGastroenterology
Description

Novel low-volume 1-litre PEG-based bowel preparation for colon cleansing prior to colonoscopy, the first 1-litre PEG product demonstrating superior high-quality cleansing compared to 2-litre alternatives.

4XIFAXAN / TARGAXAN
CategoryHepatology
Description

Rifaximin 550mg antibiotic indicated for reduction of recurrence of hepatic encephalopathy in adults, marketed as TARGAXAN in the UK.

5LYMPHOSEEK
CategoryOncology and Supportive Care
Description

Tc 99m tilmanocept radiopharmaceutical for diagnostic sentinel lymph node biopsy in adult patients with breast cancer, melanoma, or localized squamous cell carcinoma of the oral cavity.

6ENDOCUFF VISION
CategoryGastroenterology Medical Devices
Description

Single-use device attached to a colonoscope that retracts folds during withdrawal to provide optimal colon view and improve adenoma detection rates during colonoscopy.

7PEDMARQSI
CategoryRare Diseases - Oncology Supportive Care
Description

Sodium thiosulfate solution for infusion, the first and only treatment authorized for prevention of cisplatin-induced ototoxicity (hearing loss) in pediatric patients aged 1 month to under 18 years with localized, non-metastatic solid tumors.

8XOLREMDI
CategoryRare Diseases
Description

Mavorixafor, a selective CXC chemokine receptor 4 (CXCR4) antagonist, for treatment of WHIM syndrome in patients 12 years and older. First approved treatment for this ultra-rare primary immunodeficiency in the EU.

9IFINWIL
CategoryRare Diseases - Oncology
Description

Eflornithine (DFMO) treatment for high-risk neuroblastoma (HRNB), approved in Australia and Switzerland with European application under review.

10NPJ5008
CategoryRare Diseases
Description

Dantrolene sodium hemiheptahydrate treatment for malignant hyperthermia that received positive CHMP opinion for EU approval.

11KLEAN-PREP
CategoryGastroenterology
Description

Bowel preparation product for colonoscopy procedures, part of Norgine's colonoscopy and bowel cleansing portfolio.

12ANGUSTA
CategoryRare Diseases - Women's Health
Description

Misoprostol product for oral induction of labour, part of the rare disease portfolio acquired through Theravia.

13SETOFILM
CategoryOncology Supportive Care
Description

Ondansetron oral dispersible film formulation acquired from APR Applied Pharma Research S.A. for distribution in Europe, Australia and New Zealand.

14Merus Labs Portfolio
CategoryMultiple Specialty Therapy Areas
Description

Portfolio of 12 established specialty products including SINTROM, EMSELEX, ELANTAN, ISOKET, DEPONIT, SALAGEN, ESTRADERM (Europe) and VANCOCIN (Canada), acquired from Merus Labs International for C$342 million.

Scale indicator12 records

Each record includes

Type, Value, Description, Source

Partnership11 partners
Strategic tierCoreTypeOthersAnnounced on2026-05-05
Description

TGA registered PEDMARQSI for prevention of cisplatin-induced ototoxicity in pediatric patients in Australia, first and only treatment registered for this indication.

Strategic tierCoreTypeOthersAnnounced on2026-04-29
Description

European Commission granted marketing authorization for XOLREMDI following positive CHMP opinion. Approval granted under exceptional circumstances for ultra-rare WHIM syndrome.

Strategic tierCoreTypeOthersAnnounced on2026-03-26
Description

Swissmedic approved PEDMARQSI for prevention of cisplatin-induced hearing loss in children, making it the first and only treatment authorized in Switzerland for this indication.

Strategic tierMinorTypeOthersAnnounced on2026-03-05
Description

Norgine partnering with Cardiff University for student placements as part of skills and education initiatives at Hengoed facility.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-12-17
Description

Exclusive licensing agreement for chronic hepatitis delta treatment (tobevibart + elebsiran combination) in Europe, Australia, and New Zealand. Deal includes €55 million upfront payment and up to €495 million in milestone payments. Vir retains rights in US and other markets outside greater China.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-08-14
Description

Norgine completed acquisition of Theravia, a pharmaceutical company specializing in treatments for rare and debilitating conditions, to broaden portfolio and expand reach in Europe and Australia/New Zealand.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-01-13
Description

Licensing and supply agreement for XOLREMDI (mavorixafor) for WHIM syndrome in Europe, Australia, and New Zealand. Worth up to €226 million in milestones plus escalating double-digit royalties. X4 manufactures and supplies; Norgine commercializes and handles market access.

Strategic tierCoreTypeOthersAnnounced on2018-01-30
Description

Norgine owns majority stake in Arc Medical Design, originator of ENDOCUFF VISION. Subsidiary develops and provides innovative colonoscopy devices worldwide.

Strategic tierCoreTypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2018-01-29
Description

XIFAXAN/TARGAXAN licensed from Alfasigma for hepatic encephalopathy treatment in Europe. Norgine holds marketing rights in multiple European countries and Australia/New Zealand.

Strategic tierCoreTypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2018-01-11
Description

Norgine in-licensed LYMPHOSEEK (Tc 99m tilmanocept) from Navidea for commercialization and distribution in Europe and certain other key markets. Product used for sentinel lymph node biopsy in breast cancer, melanoma, and oral cancer.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2017-07-17
Description

Acquired Merus Labs International for C$342 million, adding 12 established products including SINTROM, EMSELEX, ELANTAN, ISOKET, DEPONIT, SALAGEN, ESTRADERM, and VANCOCIN.

Recent move8 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

German specialty and generics pharma group (private, sponsor-owned) with broad European portfolio across specialty, generics and consumer health. Comparable in scale, European footprint and mix of branded specialty plus mature/established products.

TypeDirect peer
Description

Public Spanish specialty pharma focused on dermatology and gastrointestinal conditions. Comparable as a European mid-cap specialty pharma with branded prescription products and a similar pan-European commercialization footprint.

TypeDirect peer
Description

Japanese-headquartered specialty pharma with significant European rare-disease operations. Comparable in its focus on rare/specialty diseases, premium orphan-drug pricing and European commercialization model.

TypeDirect peer
Description

Private Swiss specialty pharma with a strong gastroenterology and reproductive health focus. Closely comparable to Norgine as a privately held, mid-sized European specialty pharma concentrated in GI and adjacent therapeutic areas with global commercialization.

TypeDirect peer
Description

Private Italian specialty pharma that is the originator and licensor of XIFAXAN to Norgine. Highly comparable as a mid-sized European specialty pharma with GI and hepatology focus and a strong in-licensing orientation.

TypeDirect peer
Description

Swiss specialty pharma (part of Japan's Zeria Group) focused on gastroenterology, including bowel preparations and IBD treatments. Direct therapeutic overlap with Norgine's colonoscopy preparation franchise.

TypeDirect peer
Description

Public Swedish rare-disease specialty pharma with European commercialization in hematology, immunology and specialty care. Directly comparable to Norgine's expanding rare-disease franchise (XOLREMDI, PEDMARQSI, Theravia) and the European specialty go-to-market model.

TypeDirect peer
Description

German family-owned specialty pharmaceutical company focused on gastroenterology and hepatology, including bowel preparations and liver disease. Direct therapeutic-area overlap with Norgine's MOVICOL/MOVIPREP/PLENVU and XIFAXAN franchises.

TypeBroad incumbent
Description

Public French specialty pharma with broader portfolio in oncology, rare disease and consumer health. Larger and more diversified than Norgine, but overlapping in rare-disease commercialization, European footprint and specialty/GTM model.

TypeDirect peer
Description

Italian specialty pharmaceutical group with a strong rare disease and gastroenterology presence, including products for metabolic and GI conditions. Comparable European specialty platform with similar mix of branded specialty, rare disease and established products.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat6 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers3 records

Each record includes

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

Segment4 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
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles9 records

Each record includes

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

Subsidiaries10 records

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

Compliance2 records

Each record includes

Name, Class, Description

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&A3 records

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 →

Norgine

Specialty Pharmaceuticalsnorgine.com

Norgine is a privately held European specialty pharmaceutical company founded in 1906 and headquartered in Amsterdam, directly commercializing gastroenterology, hepatology, rare disease, and oncology supportive-care medicines across Europe, Australia, and New Zealand through owned manufacturing (Wales and France) and a hybrid in-licensing and acquisition growth model.

What Norgine does

Norgine is a European specialist pharmaceutical company founded in 1906 and headquartered in Amsterdam, Netherlands, with a direct commercial presence spanning all major European markets plus Australia and New Zealand. The company develops, in-licenses, manufactures, and commercializes prescription medicines across four therapeutic areas: gastroenterology (e.g., MOVICOL for constipation, MOVIPREP and PLENVU for bowel preparation prior to colonoscopy), hepatology (XIFAXAN/TARGAXAN for hepatic encephalopathy; in-licensed hepatitis delta combination with Vir Biotechnology), rare diseases (XOLREMDI for WHIM syndrome, PEDMARQSI for cisplatin-induced ototoxicity in pediatric patients, IFINWIL for high-risk neuroblastoma), and oncology supportive care and diagnostics (LYMPHOSEEK for sentinel lymph node biopsy, ENDOCUFF VISION colonoscopy device). Manufacturing is owned and operated from Hengoed, Wales (over 600 employees, approximately 50 million packs produced annually, modernized high-speed lines powered by 100% low-carbon electricity) and Dreux, France, providing supply resilience and quality control across the proprietary and select in-licensed portfolio.

The business model combines direct product sales (over €500M annual net product sales per company website, with total enterprise revenue approximately $650M per February 2026 disclosure) with licensing income, milestone payments, and royalties from partners. Revenue is generated primarily through field sales to gastroenterology, hepatology, rare disease, and oncology specialists, and through direct supply to national healthcare systems including NHS England (which funds ENDOCUFF VISION via the Innovation Technology Payment for bowel cancer screening). Growth is driven by a hybrid strategy of in-licensing and acquisitions: notable transactions include the Merus Labs acquisition in 2017 for C$342 million (adding 12 established brands including SINTROM, EMSELEX, ELANTAN, ISOKET, DEPONIT, SALAGEN, ESTRADERM, VANCOCIN), the Azanta acquisition in 2020, and the Theravia acquisition completed in August 2025 for rare disease depth, alongside licensing partnerships with X4 Pharmaceuticals (XOLREMDI), Navidea (LYMPHOSEEK), and Alfasigma (XIFAXAN/TARGAXAN). Norgine Ventures, established in 2012, provides complementary debt-like financing to innovative healthcare companies, creating a deal-flow pipeline across Europe and the US.

The company is privately held and primarily controlled by principal shareholder Peter Stein (Executive Chairman and former CEO), with institutional investment from Goldman Sachs Asset Management commencing in 2022. Leadership includes CEO Janneke van der Kamp (appointed October 2024), Chief Operating Officer Saulo Martiniano, Chief Development and Medical Officer Dr Alastair Benbow, and other regional general managers across DACH and the Netherlands. Customers include national healthcare systems across Europe and Australasia, with no single customer accounting for a dominant share of revenue; the company reports serving approximately 25 million patients annually across its portfolio. Strategic execution is supported by multiple recent regulatory wins including EU, Swissmedic, and Australian approvals for PEDMARQSI and the first-in-EU authorization of XOLREMDI under exceptional circumstances for the ultra-rare WHIM syndrome indication.

Norgine firmographics

Firmographics
Name
Norgine
Legal name
Norgine B.V.
Website
https://norgine.com
Company type
Private
Founded year
1906
Operating status
Operating
Headcount range
1,001–5,000 employees
Short description
Norgine is a privately held European specialty pharmaceutical company founded in 1906 and headquartered in Amsterdam, directly commercializing gastroenterology, hepatology, rare disease, and oncology supportive-care medicines across Europe, Australia, and New Zealand through owned manufacturing (Wales and France) and a hybrid in-licensing and acquisition growth model.
Ownership category
akta.pro rank

Norgine industry classification

Industry
Product category
Specialty Pharmaceuticals
NAICS
Pharmaceutical Preparation Manufacturing (325412), Pharmaceutical and Medicine Manufacturing (3254), Pharmaceutical and Medicine Manufacturing (32541)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
Primary Care & General Medicine Pharmaceuticals (HLAIAAAA)
akta.pro secondary industries
Generic Finished Dosage Form (FDF) Manufacturing (HLAIABAH), Infectious Disease Specialty Pharmaceuticals (Non-vaccine) (HLAIACAM)

Keywords

  • Specialty pharmaceuticals
  • Gastroenterology medicines
  • Rare disease therapeutics
  • Bowel preparation products
  • Hepatic encephalopathy treatments

Where Norgine is headquartered

Location

Headquarters

HQ city
Amsterdam
HQ country
Netherlands
HQ region
Europe

Offices5 records

Markets served

Norgine business model

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

Revenue model

  1. Net Product Sales: Direct sales of pharmaceutical products through Norgine's commercial infrastructure across Europe, Australia, and New Zealand. Products include MOVICOL, MOVIPREP, PLENVU, XIFAXAN/TARGAXAN, and others. Reported over €500 million in net product sales.
  2. Licensing Revenue: Norgine receives licensing fees and milestone payments from partners for commercialization rights in licensed territories. Also receives royalties on product sales.
  3. Manufacturing Services: Manufacturing pharmaceutical products for both proprietary portfolio and selected in-licensing partners. Operations at Hengoed, Wales and Dreux, France sites producing approximately 50 million packs annually.
  4. Strategic Investments: Norgine received £67 million strategic investment including £23 million from UK Government's Life Sciences Innovative Manufacturing Fund for Hengoed facility expansion.

Pricing tiers

ModelBillingPrice
OtherOtherXOLREMDI for WHIM syndrome - premium rare disease pricing

Go-to-market motion2 records

Distribution channels4 records

Marketing channels5 records

Norgine product offering

Product offering

Core offering

Norgine is a European specialist pharmaceutical company that develops, manufactures, and commercializes prescription medicines across gastroenterology, hepatology, rare diseases, and oncology supportive care. The company operates its own manufacturing facilities in Hengoed, Wales and Dreux, France, producing approximately 50 million packs of medicines and medical devices annually, and commercializes a portfolio that includes in-licensed and proprietary products across all major European markets, Australia, and New Zealand.

Product overview

Norgine is a leading European specialty pharmaceutical company offering a diversified portfolio of products across gastroenterology, hepatology, oncology supportive care, and rare diseases. The core portfolio includes MOVICOL® (constipation treatment), MOVIPREP® and PLENVU® (bowel preparations for colonoscopy), XIFAXAN®/TARGAXAN® (hepatic encephalopathy treatment), LYMPHOSEEK® (sentinel lymph node diagnostic), ENDOCUFF VISION® (colonoscopy device), PEDMARQSI® (pediatric ototoxicity prevention), XOLREMDI® (WHIM syndrome treatment), and IFINWIL® (neuroblastoma treatment). The company operates through direct commercialization in Europe and Australia with over €500 million in net product sales.

Differentiator

Problem solved

Functional benefit

Brands

  • Norgine Ventures: Complementary business established in 2012 supporting innovative healthcare companies through debt-like financing in Europe and the US
  • Theravia

Products and services

  • MOVICOL Leading anti-constipation treatment for chronic constipation, sold primarily in European markets and Australia.
  • MOVIPREP Two-litre PEG-based bowel preparation for adults prior to colonoscopy procedures.
  • PLENVU Novel low-volume 1-litre PEG-based bowel preparation for colon cleansing prior to colonoscopy, the first 1-litre PEG product demonstrating superior high-quality cleansing compared to 2-litre alternatives.
  • XIFAXAN / TARGAXAN Rifaximin 550mg antibiotic indicated for reduction of recurrence of hepatic encephalopathy in adults, marketed as TARGAXAN in the UK.
  • LYMPHOSEEK Tc 99m tilmanocept radiopharmaceutical for diagnostic sentinel lymph node biopsy in adult patients with breast cancer, melanoma, or localized squamous cell carcinoma of the oral cavity.
  • ENDOCUFF VISION Single-use device attached to a colonoscope that retracts folds during withdrawal to provide optimal colon view and improve adenoma detection rates during colonoscopy.
  • PEDMARQSI Sodium thiosulfate solution for infusion, the first and only treatment authorized for prevention of cisplatin-induced ototoxicity (hearing loss) in pediatric patients aged 1 month to under 18 years with localized, non-metastatic solid tumors.
  • XOLREMDI Mavorixafor, a selective CXC chemokine receptor 4 (CXCR4) antagonist, for treatment of WHIM syndrome in patients 12 years and older. First approved treatment for this ultra-rare primary immunodeficiency in the EU.
  • IFINWIL Eflornithine (DFMO) treatment for high-risk neuroblastoma (HRNB), approved in Australia and Switzerland with European application under review.
  • NPJ5008 Dantrolene sodium hemiheptahydrate treatment for malignant hyperthermia that received positive CHMP opinion for EU approval.
  • KLEAN-PREP Bowel preparation product for colonoscopy procedures, part of Norgine's colonoscopy and bowel cleansing portfolio.
  • ANGUSTA Misoprostol product for oral induction of labour, part of the rare disease portfolio acquired through Theravia.
  • SETOFILM Ondansetron oral dispersible film formulation acquired from APR Applied Pharma Research S.A. for distribution in Europe, Australia and New Zealand.
  • Merus Labs Portfolio Portfolio of 12 established specialty products including SINTROM, EMSELEX, ELANTAN, ISOKET, DEPONIT, SALAGEN, ESTRADERM (Europe) and VANCOCIN (Canada), acquired from Merus Labs International for C$342 million.

Quantifiable outcome

  • 88% undetectable viral response at 96 weeks in Phase 2 hepatitis delta combination regimen (Vir Biotechnology data)
  • +5 more outcomes

Companies that use Norgine

Customer profile

Named customers3 records

Segments4 records

Ideal customer profiles2 records

Norgine technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

Norgine partnerships and signals

Strategic signal

Partnerships

Eleven partnerships are on record, tiered core and minor.

  • Therapeutic Goods Administration (TGA) AustraliacoreOthers · 5 May 2026TGA registered PEDMARQSI for prevention of cisplatin-induced ototoxicity in pediatric patients in Australia, first and only treatment registered for this indication.
  • European Commission / EMAcoreOthers · 29 April 2026European Commission granted marketing authorization for XOLREMDI following positive CHMP opinion. Approval granted under exceptional circumstances for ultra-rare WHIM syndrome.
  • SwissmediccoreOthers · 26 March 2026Swissmedic approved PEDMARQSI for prevention of cisplatin-induced hearing loss in children, making it the first and only treatment authorized in Switzerland for this indication.
  • Cardiff UniversityminorOthers · 5 March 2026Norgine partnering with Cardiff University for student placements as part of skills and education initiatives at Hengoed facility.
  • Vir BiotechnologycoreStrategic or Co-development Partner · 17 December 2025Exclusive licensing agreement for chronic hepatitis delta treatment (tobevibart + elebsiran combination) in Europe, Australia, and New Zealand. Deal includes €55 million upfront payment and up to €495 million in milestone payments. Vir retains rights in US and other markets outside greater China.
  • TheraviacoreStrategic or Co-development Partner · 14 August 2025Norgine completed acquisition of Theravia, a pharmaceutical company specializing in treatments for rare and debilitating conditions, to broaden portfolio and expand reach in Europe and Australia/New Zealand.
  • X4 PharmaceuticalscoreStrategic or Co-development Partner · 13 January 2025Licensing and supply agreement for XOLREMDI (mavorixafor) for WHIM syndrome in Europe, Australia, and New Zealand. Worth up to €226 million in milestones plus escalating double-digit royalties. X4 manufactures and supplies; Norgine commercializes and handles market access.
  • Arc Medical Design LtdcoreOthers · 30 January 2018Norgine owns majority stake in Arc Medical Design, originator of ENDOCUFF VISION. Subsidiary develops and provides innovative colonoscopy devices worldwide.
  • Alfasigma S.p.A.coreOEM/ Whitelabel/ Licensing Partner · 29 January 2018XIFAXAN/TARGAXAN licensed from Alfasigma for hepatic encephalopathy treatment in Europe. Norgine holds marketing rights in multiple European countries and Australia/New Zealand.
  • Navidea Biopharmaceuticals InccoreOEM/ Whitelabel/ Licensing Partner · 11 January 2018Norgine in-licensed LYMPHOSEEK (Tc 99m tilmanocept) from Navidea for commercialization and distribution in Europe and certain other key markets. Product used for sentinel lymph node biopsy in breast cancer, melanoma, and oral cancer.
  • Merus Labs International Inc.coreStrategic or Co-development Partner · 17 July 2017Acquired Merus Labs International for C$342 million, adding 12 established products including SINTROM, EMSELEX, ELANTAN, ISOKET, DEPONIT, SALAGEN, ESTRADERM, and VANCOCIN.

Scale indicators12 records

Recent moves8 records

Expansion highlights6 records

Norgine competitors and assessment

Company assessment

Broad incumbents

  • Stada Arzneimittel: German specialty and generics pharma group (private, sponsor-owned) with broad European portfolio across specialty, generics and consumer health. Comparable in scale, European footprint and mix of branded specialty plus mature/established products.
  • Ipsen: Public French specialty pharma with broader portfolio in oncology, rare disease and consumer health. Larger and more diversified than Norgine, but overlapping in rare-disease commercialization, European footprint and specialty/GTM model.

Direct peers

  • Almirall: Public Spanish specialty pharma focused on dermatology and gastrointestinal conditions. Comparable as a European mid-cap specialty pharma with branded prescription products and a similar pan-European commercialization footprint.
  • Kyowa Kirin: Japanese-headquartered specialty pharma with significant European rare-disease operations. Comparable in its focus on rare/specialty diseases, premium orphan-drug pricing and European commercialization model.
  • Ferring Pharmaceuticals: Private Swiss specialty pharma with a strong gastroenterology and reproductive health focus. Closely comparable to Norgine as a privately held, mid-sized European specialty pharma concentrated in GI and adjacent therapeutic areas with global commercialization.
  • Alfasigma: Private Italian specialty pharma that is the originator and licensor of XIFAXAN to Norgine. Highly comparable as a mid-sized European specialty pharma with GI and hepatology focus and a strong in-licensing orientation.
  • Tillotts Pharma: Swiss specialty pharma (part of Japan's Zeria Group) focused on gastroenterology, including bowel preparations and IBD treatments. Direct therapeutic overlap with Norgine's colonoscopy preparation franchise.
  • Swedish Orphan Biovitrum (Sobi): Public Swedish rare-disease specialty pharma with European commercialization in hematology, immunology and specialty care. Directly comparable to Norgine's expanding rare-disease franchise (XOLREMDI, PEDMARQSI, Theravia) and the European specialty go-to-market model.
  • Dr. Falk Pharma: German family-owned specialty pharmaceutical company focused on gastroenterology and hepatology, including bowel preparations and liver disease. Direct therapeutic-area overlap with Norgine's MOVICOL/MOVIPREP/PLENVU and XIFAXAN franchises.
  • Recordati: Italian specialty pharmaceutical group with a strong rare disease and gastroenterology presence, including products for metabolic and GI conditions. Comparable European specialty platform with similar mix of branded specialty, rare disease and established products.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat6 records

Key risks6 records

Key highlights7 records

Customer concentration

Norgine social profiles

Digital presence

Norgine compliance and trust

Trust signal

Compliance2 records

Norgine financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Norgine leadership team

Management profile

Number of profiles

Profiles9 records

Norgine subsidiaries and ownership

Company hierarchy

Subsidiaries10 records

Norgine funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

Norgine M&A and investment

M&A and investment

M&A3 records

Investments

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

Frequently asked questions about Norgine

What does Norgine do?

Norgine is a European specialist pharmaceutical company that develops, manufactures, and commercializes prescription medicines across gastroenterology, hepatology, rare diseases, and oncology supportive care. The company operates its own manufacturing facilities in Hengoed, Wales and Dreux, France, producing approximately 50 million packs of medicines and medical devices annually, and commercializes a portfolio that includes in-licensed and proprietary products across all major European markets, Australia, and New Zealand.

Is Norgine a public or private company?

Norgine is a private company. It is classified as family owned and is currently operating.

When was Norgine founded?

Norgine was founded in 1906. It employs 1,001 to 5,000 people.

Where is Norgine based?

Norgine is headquartered in Amsterdam, Netherlands, in the Europe region.

How does Norgine make money?

Four revenue lines are on record. Net Product Sales are the primary driver. The others are licensing Revenue, manufacturing Services and strategic Investments.

Who are Norgine's main competitors?

Broad incumbents on record are Stada Arzneimittel and Ipsen. Direct peers are Almirall, Kyowa Kirin, Ferring Pharmaceuticals, Alfasigma, Tillotts Pharma, Swedish Orphan Biovitrum (Sobi), Dr. Falk Pharma and Recordati.

Does Norgine have an API?

No public API is recorded for Norgine.

What industry is Norgine in?

Norgine's product category is Specialty Pharmaceuticals. Its primary akta.pro industry code is HLAIAAAA, Primary Care & General Medicine Pharmaceuticals, with a secondary code of HLAIABAH, Generic Finished Dosage Form (FDF) Manufacturing. Its NAICS code is 325412 and its SIC code is 2834.

Unlock the full company data

50 free credits on sign-up, no credit card required.

Contact sales
Live signals
Investing.comVir Bio Q2 2026 slides: hepatitis delta nears approval, oncology gains By Investing.comVir Biotechnology reported Q2 2026 net income of $80.1 million, a dramatic turnaround from a loss of $111.0 million in the same period last year, driven by $238.9 million in license and collaboration revenue from partnerships with Astellas and Norgine. The company's chronic hepatitis delta combination therapy (elebsiran and tobevibart) achieved 88% undetectable HDV RNA at 96 weeks in the Phase 2 SOLSTICE trial, positioning it for potential approval as the company advances three Phase 3 ECLIPSE trials with topline data expected in Q4 2026.Stock TitanX4 Pharma Q1 cash $233.7M, runway through 2028X4 Pharmaceuticals reported a Q1 2026 net loss of $20.2 million compared to net income of $0.3 million in Q1 2025, with revenue declining to $2.7 million from $28.8 million primarily due to one-time license revenue from Norgine recognized in the prior year period. The company announced the European Commission granted marketing authorization for XOLREMDI (mavorixafor) for the treatment of WHIM syndrome in the European Union, with European commercialization to be led by partner Norgine, and reported cash reserves of $233.7 million providing operational runway through 2028. The pivotal 4WARD Phase 3 trial of mavorixafor in chronic neutropenia remains on track to complete enrollment by the end of Q3 2026.PR Newswire APACNorgine welcomes TGA registration in Australia of PEDMARQSI® (sodium thiosulfate anhydrous) for the prevention of cisplatin-induced hearing loss in children1Norgine announced that PEDMARQSI (sodium thiosulfate anhydrous) received TGA registration in Australia for preventing cisplatin-induced hearing loss in children aged 1 month to under 18 with localized solid tumors. The approval is based on two Phase 3 trials and is the first and only treatment registered in Australia for this indication. The drug is not on the Pharmaceutical Benefits Scheme.PR Newswire APACNorgine welcomes TGA registration in Australia of PEDMARQSI® (sodium thiosulfate anhydrous) for the prevention of cisplatin-induced hearing loss in children1Norgine announced that PEDMARQSI (sodium thiosulfate anhydrous) received TGA registration in Australia for preventing cisplatin-induced hearing loss in children aged 1 month to under 18 with solid tumours. The approval is based on two Phase 3 trials and is the first and only treatment registered in Australia for this indication. The drug is not on the Pharmaceutical Benefits Scheme.BioSpaceNorgine welcomes TGA registration in Australia of PEDMARQSI® (sodium thiosulfate anhydrous) for the prevention of cisplatin-induced hearing loss in children1Norgine announced TGA registration of PEDMARQSI (sodium thiosulfate anhydrous) for preventing cisplatin-induced hearing loss in children aged 1 month to <18 years with solid tumours. The approval is based on two Phase 3 trials and is the first and only such treatment in Australia. The drug is not on the Pharmaceutical Benefits Scheme.GlobeNewswireX4 Pharmaceuticals Reports First Quarter 2026 Financial Results and Provides Corporate UpdateX4 Pharmaceuticals reported Q1 2026 results with a $2.7 million revenue and a $20.2 million net loss, and announced the European Commission's approval of XOLREMDI for WHIM syndrome. The company expects to complete enrollment in its 4WARD Phase 3 trial by Q3 2026 and has a cash runway through 2028.Investing.comVir Biotech Q1 2026 presentation: $2.2B partnerships fuel oncology pivot By Investing.comVir Biotechnology presented its Q1 2026 corporate overview on May 6, 2026, reporting a net loss of $125.7 million with EPS of -$0.85 significantly missing analyst forecasts by -750%, despite disciplined cost management with operating expenses declining 7% year-over-year. The biotech announced two landmark collaborations totaling up to $2.2 billion — a $1.7 billion partnership with Astellas for prostate cancer drug VIR-5500 and a €550 million deal with Norgine for chronic hepatitis delta therapy in Europe, Australia, and New Zealand — extending the company's cash runway into the second half of 2028. Clinical milestones include Phase 3 ECLIPSE trial topline data for CHD combination therapy expected Q4 2026, and Phase 1 expansion cohorts for VIR-5500 initiated in Q2 2026 following breakthrough results in heavily pretreated prostate cancer patients.PR NewswireNorgine se félicite de l'enregistrement par la TGA en Australie de PEDMARQSI® (thiosulfate de sodium anhydre) pour la prévention de la perte auditive induite par le cisplatine chez les enfants1Norgine announced that its drug PEDMARQSI® (anhydrous sodium thiosulfate) has been registered by Australia's Therapeutic Goods Administration (TGA) for the prevention of cisplatin-induced ototoxicity in pediatric patients aged 1 month to under 18 years with localized, non-metastatic solid tumors. PEDMARQSI® is the first and only registered treatment in Australia specifically for preventing cisplatin-induced hearing loss in this patient population. The TGA registration was based on data from two open-label, randomized Phase III clinical trials, SIOPEL 6 and COG ACCL0431, and follows prior approvals by the European Medicines Agency, the UK's MHRA, and Swissmedic.PR NewswireNorgine welcomes TGA registration in Australia of PEDMARQSI® (sodium thiosulfate anhydrous) for the prevention of cisplatin-induced hearing loss in children1Norgine announced that its drug PEDMARQSI® (sodium thiosulfate anhydrous) has been registered by the Australian Therapeutic Goods Administration (TGA) for the prevention of ototoxicity induced by cisplatin chemotherapy in pediatric patients aged 1 month to under 18 years with localized, non-metastatic solid tumors. PEDMARQSI® is the first and only treatment registered in Australia for the prevention of cisplatin-induced hearing loss in children, addressing a significant unmet medical need in pediatric oncology supportive care. The registration was based on data from two Phase 3 clinical trials (SIOPEL 6 and COG ACCL0431), and adds to previous approvals in Europe, the United Kingdom, and Switzerland.PR NewswireNorgine welcomes TGA registration in Australia of PEDMARQSI® (sodium thiosulfate anhydrous) for the prevention of cisplatin-induced hearing loss in children1Norgine announced that PEDMARQSI® (sodium thiosulfate anhydrous) has been registered by Australia's Therapeutic Goods Administration for the prevention of cisplatin-induced ototoxicity in pediatric patients aged 1 month to under 18 years with localised, non-metastatic solid tumours. The drug is the first and only treatment registered in Australia for this indication, with registration based on data from two Phase 3 clinical trials, SIOPEL 6 and COG ACCL0431. PEDMARQSI® is not currently included on the Pharmaceutical Benefits Scheme, and the approval adds to existing marketing authorisations in the European Union, United Kingdom, and Switzerland.