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CSL Vifor

Full company profile

uuid0006ow6

Namestring
CSL Vifor
Legal namestring
CSL Limited
Websiteurl
viforpharma.com
Company typeenum
Public
Founded yearint
2022
Descriptiontext

CSL Vifor is a global pharmaceutical business unit of CSL Limited (ASX: CSL), specializing in iron deficiency and nephrology therapies. Formed in August 2022 when CSL acquired Vifor Pharma for approximately $11 billion, the unit traces its heritage to 1872 in St. Gallen, Switzerland. It sells a focused portfolio including Ferinject/Injectafer (ferric carboxymaltose, approved in 87 countries), Venofer (iron sucrose, 85 countries), Maltofer (oral iron polymaltose, 76 countries), Velphoro (sucroferric oxyhydroxide, 50 countries), Mircera (long-acting erythropoiesis-stimulating agent licensed from Roche), Retacrit (epoetin alfa biosimilar licensed from Pfizer), Veltassa (patiromer), Tavneos (avacopan), Korsuva/Kapruvia (difelikefalin), Rayaldee (prolonged-release calcifediol), and Filspari (sparsentan). The nephrology portfolio is co-developed and co-commercialized through the Vifor Fresenius Medical Care Renal Pharma joint company.

The business operates two principal therapeutic segments: iron deficiency and iron deficiency anaemia (addressing heart failure, chronic kidney disease, gastroenterology, inflammatory bowel disease, patient blood management, and women's health), and nephrology (spanning all stages of kidney disease from preservation of renal function through dialysis complication management). Products are distributed through CSL Vifor's own sales organization in over 100 countries, supplemented by regional licensing and distribution partnerships (Otsuka in Canada, Kissei in Japan, CTS in the Middle East/Israel) and the Fresenius Medical Care joint venture, which supplies Mircera to over 6,500 dialysis clinics in the USA.

Revenue is generated primarily through direct pharmaceutical product sales and licensing royalties from in-licensed assets. Manufacturing is anchored at St. Gallen and Ettingen in Switzerland, with R&D laboratory operations in Schlieren. The company's go-to-market is enterprise field sales oriented toward specialists (nephrologists, hematologists, gastroenterologists) reinforced by participation in major medical congresses (ERA, ASN Kidney Week, NATA, EULAR, ESAIC) and a dedicated Science Hub for healthcare professionals. Strategic positioning rests on 150+ years of brand heritage in iron therapy, deep regulatory footprint across 50–87 countries per product, and structural access to the Fresenius dialysis channel.

Short descriptiontext

CSL Vifor is a global pharmaceutical business unit of CSL Limited that develops and markets iron deficiency and nephrology therapies across 100+ countries, serving specialists and dialysis networks through proprietary products, in-licensed assets, and a joint venture with Fresenius Medical Care.

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

Serves global market

Offices3 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
iron deficiency therapy, nephrology pharmaceuticals, intravenous iron, kidney disease treatments, specialty pharma manufacturing
Industry1 code
1Cardiology & Vascular Specialty Pharmaceuticals
CodeHLAIACAGPrimaryYes
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Specialty Pharmaceuticals — Iron Deficiency and Nephrology
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model2 records
1Pharmaceutical Product Sales
TypeOne Time License
Description

CSL Vifor generates revenue through manufacturing and marketing pharmaceutical products globally in iron deficiency and nephrology therapeutic areas. Products are distributed through their own sales organization and distribution partners across over 100 countries.

csl.com
2Licensing Royalties
TypeLicensing Royalties
Description

Revenue from licensing agreements including Mircera (licensed from F. Hoffmann-La Roche AG since 2015) and Retacrit (licensed from Pfizer, Inc., approved in USA since 2018). These arrangements provide royalty streams from partner commercialization.

csl.com
Marketing channels3 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
Supply Chain, Operations, Personnel, Technology or R&D, Marketing or Sales, Infrastructure
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 13 records shown
1Ferinject
Description

Ferric Carboxymaltose Intravenous Iron - for iron deficiency and iron deficiency anaemia

csl.com
+12 more records
Core offering1 text field

CSL Vifor develops, manufactures and markets prescription pharmaceutical products for iron deficiency and iron deficiency anaemia across heart failure, kidney disease, gastroenterology, inflammatory bowel disease, patient blood management and women's health, as well as nephrology therapies covering the full spectrum of kidney disease. The company distributes these products globally, supplemented by in-licensed assets and a joint nephrology venture with Fresenius Medical Care.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • Ferinject approved in 87 countries
+3 more records
Product overview1 text field

CSL Vifor is a global pharmaceutical company specializing in iron deficiency and nephrology therapies. The company operates across two primary therapeutic areas: Iron Deficiency (including iron deficiency anaemia) with products Ferinject®, Venofer®, and Maltofer®; and Nephrology with products including Veltassa®, Rayaldee®, Tavneos®, Mircera®, Retacrit®, Velphoro®, Korsuva®, and Filspari®. The company also partners with Vifor Fresenius Medical Care Renal Pharma for nephrology solutions. With a presence in over 100 countries, CSL Vifor focuses on strategic global partnering, in-licensing, developing, manufacturing, and marketing pharmaceutical products for precision healthcare.

Product and service11 records
1Ferinject / Injectafer (Ferric Carboxymaltose)
CategoryIron deficiency therapy
Description

Intravenous iron therapy for the treatment of iron deficiency and iron deficiency anaemia across multiple therapeutic areas including heart failure, kidney disease, gastroenterology, inflammatory bowel disease, patient blood management and women's health. Marketed as Ferinject internationally and as Injectafer in the USA; approved in 87 countries.

2Venofer (Iron Sucrose)
CategoryIron deficiency therapy
Description

Low-dose intravenous iron therapy for the treatment of iron deficiency in patients with chronic kidney disease and other conditions. Approved in 85 countries.

3Maltofer (Oral Iron Polymaltose Complex)
CategoryIron deficiency therapy
Description

Oral iron therapy for the treatment of iron deficiency and iron deficiency anaemia. Approved in 76 countries.

4Veltassa (Patiromer)
CategoryNephrology therapy
Description

Potassium binder for the treatment of hyperkalemia in nephrology patients. Available in 16 countries.

5Rayaldee (Prolonged-release Calcifediol)
CategoryNephrology therapy
Description

Prolonged-release formulation of calcifediol for the management of secondary hyperparathyroidism in patients with chronic kidney disease. Launched in Germany and Switzerland.

6Tavneos (Avacopan)
CategoryNephrology therapy
Description

Oral elective inhibitor of C5aR1 for the treatment of ANCA-associated vasculitis. Approved in EU, UK, Switzerland, Australia, UAE, Kuwait, and Israel; launched in major EU markets, Australia, Japan (via Kissei) and Canada (via Otsuka).

7Mircera (Methoxypolyethylene Glycol Epoetin Beta)
CategoryNephrology therapy
Description

Long-acting erythropoiesis-stimulating agent licensed from F. Hoffmann-La Roche AG since 2015 for the treatment of anaemia associated with chronic kidney disease. Supplied to over 6,500 dialysis clinics in the USA and its territories.

8Retacrit (Epoetin Alfa-epbx)
CategoryNephrology therapy
Description

Epoetin alfa biosimilar licensed from Pfizer, Inc. and approved in the USA since 2018 for all indications of the reference drug epoetin alfa, used to treat anaemia associated with chronic kidney disease and chemotherapy.

9Velphoro (Sucroferric Oxyhydroxide)
CategoryNephrology therapy
Description

Iron-based phosphate binder for the management of hyperphosphatemia in dialysis patients. Approved in 50 countries.

10Korsuva / Kapruvia (Difelikefalin)
CategoryNephrology therapy
Description

Peripherally restricted kappa opioid receptor agonist for the treatment of pruritus in dialysis patients. Approved in US, EU, UK, Switzerland, Canada, Australia, UAE, Kuwait, Israel, and Singapore; launched in major EU markets, Germany, Austria, Sweden, France, UK, Canada, Australia, UAE, Kuwait and Israel.

11Filspari (Sparsentan)
CategoryNephrology therapy
Description

Dual endothelin-angiotensin receptor antagonist for the treatment of primary immunoglobulin A nephropathy. Approved in EU, UK, and Switzerland; launched in Germany, UK, Austria and Switzerland.

Scale indicator6 records

Each record includes

Type, Value, Description, Source

Partnership7 partners
Strategic tierCoreTypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2018-01-01
Description

Licensed Retacrit (Epoetin Alfa-epbx) from Pfizer, approved in the USA since 2018 for all indications of its reference drug, epoetin alfa.

Strategic tierCoreTypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2015-01-01
Description

Licensed Mircera (long-acting erythropoiesis-stimulating agent) from Roche since 2015. The product is currently supplied to over 6,500 dialysis clinics in the USA and its territories.

3Vifor Fresenius Medical Care Renal Pharma
Strategic tierCoreTypeStrategic or Co-development Partner
Description

Joint company partnership for nephrology products. Together with Vifor Fresenius Medical Care Renal Pharma, CSL Vifor has a strong and rapidly growing presence in nephrology, committed to launching the next generation of therapies to address the full spectrum of kidney disease.

csl.com
Strategic tierRegionalTypeChannel Partner/ Reseller/ Distributor
Description

Kissei distributes Tavneos (Avacopan) in Japan for treatment of ANCA-associated vasculitis.

Strategic tierRegionalTypeChannel Partner/ Reseller/ Distributor
Description

Otsuka distributes Tavneos in Canada and Korsuva (Difelikefalin) in Canada.

Strategic tierRegionalTypeChannel Partner/ Reseller/ Distributor
Description

CTS distributes Korsuva (Difelikefalin) in Israel as part of the Middle East partnership.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

CSL has long participated in the WFH Humanitarian Aid Program to bring needed medicines to underserved parts of the world. CSL is also proud to support the WFH Path to Access to Care and Treatment (PACT) Program to advance diagnosis, enhance training and advocacy to improve national care. This aligns with CSL's commitment to improve access and equity for patients.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Global pharma with rare disease, vaccines, and specialty therapeutics franchises overlapping with CSL Vifor's nephrology and iron deficiency focus. Comparable as a broad incumbent across specialty pharma distribution channels.

TypeBroad incumbent
Description

Licensor of Retacrit (epoetin alfa biosimilar) to CSL Vifor and a global biopharmaceutical incumbent with significant nephrology and biosimilars portfolio. Comparable as a counterparty in CSL Vifor's licensing strategy and as a broad peer in renal anemia.

TypeEmerging player
Description

U.S. biopharma focused on HIF-PHI inhibitors (vadadustat) for anemia in CKD, directly competing with CSL Vifor's ESA/iron franchise. Comparable as an emerging nephrology specialist targeting the same patient population.

4Vifor Fresenius Medical Care Renal Pharma
TypeDirect peer
Description

Joint venture between CSL Vifor and Fresenius Medical Care focused exclusively on nephrology products. Comparable as the closest direct peer in nephrology since it shares CSL Vifor's portfolio strategy and channel access.

TypeBroad incumbent
Description

Originator of Mircera (licensed to CSL Vifor) and a major nephrology and biologics player. Comparable as the licensor of a core CSL Vifor product and as a broader specialty pharma incumbent in nephrology.

TypeEmerging player
Description

Developer of tenapanor and other renal/cardio-renal therapies, with overlap in nephrology patient segments addressed by Veltassa and Velphoro. Comparable as a focused emerging player in CKD complications.

TypeBroad incumbent
Description

Large biotech with established ESA franchise (Epogen/Aranesp) in the same nephrology anemia market CSL Vifor addresses via Mircera and Retacrit. Comparable as a specialty pharma incumbent in iron/ESA-adjacent nephrology therapeutics.

TypeBroad incumbent
Description

Major pharma with specialty and rare disease franchises, including cardiovascular and nephrology adjacencies. Comparable as a broad incumbent competing for the same specialist prescriber audience in CKD and heart failure.

TypeBroad incumbent
Description

Global pharma with rare disease and specialty therapeutics overlap to CSL Vifor's nephrology portfolio. Comparable as a broad incumbent with product adjacencies in iron deficiency and rare renal indications; co-founding supporter of WFH humanitarian programs.

TypeDirect peer
Description

World's largest dialysis services and products company and CSL Vifor's joint venture partner in Vifor Fresenius Medical Care Renal Pharma. Closely comparable given shared nephrology focus, shared commercial channel into U.S. dialysis clinics, and overlapping patient populations.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 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 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 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

Feature2 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Subsidiaries1 record

Each record includes

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

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 →

CSL Vifor

Specialty Pharmaceuticals — Iron Deficiency and Nephrologyviforpharma.com

CSL Vifor is a global pharmaceutical business unit of CSL Limited that develops and markets iron deficiency and nephrology therapies across 100+ countries, serving specialists and dialysis networks through proprietary products, in-licensed assets, and a joint venture with Fresenius Medical Care.

What CSL Vifor does

CSL Vifor is a global pharmaceutical business unit of CSL Limited (ASX: CSL), specializing in iron deficiency and nephrology therapies. Formed in August 2022 when CSL acquired Vifor Pharma for approximately $11 billion, the unit traces its heritage to 1872 in St. Gallen, Switzerland. It sells a focused portfolio including Ferinject/Injectafer (ferric carboxymaltose, approved in 87 countries), Venofer (iron sucrose, 85 countries), Maltofer (oral iron polymaltose, 76 countries), Velphoro (sucroferric oxyhydroxide, 50 countries), Mircera (long-acting erythropoiesis-stimulating agent licensed from Roche), Retacrit (epoetin alfa biosimilar licensed from Pfizer), Veltassa (patiromer), Tavneos (avacopan), Korsuva/Kapruvia (difelikefalin), Rayaldee (prolonged-release calcifediol), and Filspari (sparsentan). The nephrology portfolio is co-developed and co-commercialized through the Vifor Fresenius Medical Care Renal Pharma joint company.

The business operates two principal therapeutic segments: iron deficiency and iron deficiency anaemia (addressing heart failure, chronic kidney disease, gastroenterology, inflammatory bowel disease, patient blood management, and women's health), and nephrology (spanning all stages of kidney disease from preservation of renal function through dialysis complication management). Products are distributed through CSL Vifor's own sales organization in over 100 countries, supplemented by regional licensing and distribution partnerships (Otsuka in Canada, Kissei in Japan, CTS in the Middle East/Israel) and the Fresenius Medical Care joint venture, which supplies Mircera to over 6,500 dialysis clinics in the USA.

Revenue is generated primarily through direct pharmaceutical product sales and licensing royalties from in-licensed assets. Manufacturing is anchored at St. Gallen and Ettingen in Switzerland, with R&D laboratory operations in Schlieren. The company's go-to-market is enterprise field sales oriented toward specialists (nephrologists, hematologists, gastroenterologists) reinforced by participation in major medical congresses (ERA, ASN Kidney Week, NATA, EULAR, ESAIC) and a dedicated Science Hub for healthcare professionals. Strategic positioning rests on 150+ years of brand heritage in iron therapy, deep regulatory footprint across 50–87 countries per product, and structural access to the Fresenius dialysis channel.

CSL Vifor firmographics

Firmographics
Name
CSL Vifor
Legal name
CSL Limited
Website
https://viforpharma.com
Company type
Public
Founded year
2022
Operating status
Operating
Headcount range
1,001–5,000 employees
Short description
CSL Vifor is a global pharmaceutical business unit of CSL Limited that develops and markets iron deficiency and nephrology therapies across 100+ countries, serving specialists and dialysis networks through proprietary products, in-licensed assets, and a joint venture with Fresenius Medical Care.
Ownership category
akta.pro rank

CSL Vifor industry classification

Industry
Product category
Specialty Pharmaceuticals — Iron Deficiency and Nephrology
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
Cardiology & Vascular Specialty Pharmaceuticals (HLAIACAG)

Keywords

  • Iron deficiency therapy
  • Nephrology pharmaceuticals
  • Intravenous iron
  • Kidney disease treatments
  • Specialty pharma manufacturing

Where CSL Vifor is headquartered

Location

Headquarters

HQ city
Glattbrugg
HQ country
Switzerland
HQ region
Europe

Offices3 records

Markets served

CSL Vifor business model

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

Revenue model

  1. Pharmaceutical Product Sales: CSL Vifor generates revenue through manufacturing and marketing pharmaceutical products globally in iron deficiency and nephrology therapeutic areas. Products are distributed through their own sales organization and distribution partners across over 100 countries.
  2. Licensing Royalties: Revenue from licensing agreements including Mircera (licensed from F. Hoffmann-La Roche AG since 2015) and Retacrit (licensed from Pfizer, Inc., approved in USA since 2018). These arrangements provide royalty streams from partner commercialization.

Go-to-market motion2 records

Distribution channels4 records

Marketing channels3 records

CSL Vifor product offering

Product offering

Core offering

CSL Vifor develops, manufactures and markets prescription pharmaceutical products for iron deficiency and iron deficiency anaemia across heart failure, kidney disease, gastroenterology, inflammatory bowel disease, patient blood management and women's health, as well as nephrology therapies covering the full spectrum of kidney disease. The company distributes these products globally, supplemented by in-licensed assets and a joint nephrology venture with Fresenius Medical Care.

Product overview

CSL Vifor is a global pharmaceutical company specializing in iron deficiency and nephrology therapies. The company operates across two primary therapeutic areas: Iron Deficiency (including iron deficiency anaemia) with products Ferinject®, Venofer®, and Maltofer®; and Nephrology with products including Veltassa®, Rayaldee®, Tavneos®, Mircera®, Retacrit®, Velphoro®, Korsuva®, and Filspari®. The company also partners with Vifor Fresenius Medical Care Renal Pharma for nephrology solutions. With a presence in over 100 countries, CSL Vifor focuses on strategic global partnering, in-licensing, developing, manufacturing, and marketing pharmaceutical products for precision healthcare.

Differentiator

Problem solved

Functional benefit

Brands

  • Ferinject: Ferric Carboxymaltose Intravenous Iron - for iron deficiency and iron deficiency anaemia
  • Injectafer
  • Venofer
  • Maltofer
  • Veltassa
  • Rayaldee
  • Tavneos
  • Mircera
  • Retacrit
  • Velphoro
  • Korsuva
  • Kapruvia
  • Filspari

Products and services

  • Ferinject / Injectafer (Ferric Carboxymaltose) Intravenous iron therapy for the treatment of iron deficiency and iron deficiency anaemia across multiple therapeutic areas including heart failure, kidney disease, gastroenterology, inflammatory bowel disease, patient blood management and women's health. Marketed as Ferinject internationally and as Injectafer in the USA; approved in 87 countries.
  • Venofer (Iron Sucrose) Low-dose intravenous iron therapy for the treatment of iron deficiency in patients with chronic kidney disease and other conditions. Approved in 85 countries.
  • Maltofer (Oral Iron Polymaltose Complex) Oral iron therapy for the treatment of iron deficiency and iron deficiency anaemia. Approved in 76 countries.
  • Veltassa (Patiromer) Potassium binder for the treatment of hyperkalemia in nephrology patients. Available in 16 countries.
  • Rayaldee (Prolonged-release Calcifediol) Prolonged-release formulation of calcifediol for the management of secondary hyperparathyroidism in patients with chronic kidney disease. Launched in Germany and Switzerland.
  • Tavneos (Avacopan) Oral elective inhibitor of C5aR1 for the treatment of ANCA-associated vasculitis. Approved in EU, UK, Switzerland, Australia, UAE, Kuwait, and Israel; launched in major EU markets, Australia, Japan (via Kissei) and Canada (via Otsuka).
  • Mircera (Methoxypolyethylene Glycol Epoetin Beta) Long-acting erythropoiesis-stimulating agent licensed from F. Hoffmann-La Roche AG since 2015 for the treatment of anaemia associated with chronic kidney disease. Supplied to over 6,500 dialysis clinics in the USA and its territories.
  • Retacrit (Epoetin Alfa-epbx) Epoetin alfa biosimilar licensed from Pfizer, Inc. and approved in the USA since 2018 for all indications of the reference drug epoetin alfa, used to treat anaemia associated with chronic kidney disease and chemotherapy.
  • Velphoro (Sucroferric Oxyhydroxide) Iron-based phosphate binder for the management of hyperphosphatemia in dialysis patients. Approved in 50 countries.
  • Korsuva / Kapruvia (Difelikefalin) Peripherally restricted kappa opioid receptor agonist for the treatment of pruritus in dialysis patients. Approved in US, EU, UK, Switzerland, Canada, Australia, UAE, Kuwait, Israel, and Singapore; launched in major EU markets, Germany, Austria, Sweden, France, UK, Canada, Australia, UAE, Kuwait and Israel.
  • Filspari (Sparsentan) Dual endothelin-angiotensin receptor antagonist for the treatment of primary immunoglobulin A nephropathy. Approved in EU, UK, and Switzerland; launched in Germany, UK, Austria and Switzerland.

Quantifiable outcome

  • Ferinject approved in 87 countries
  • +3 more outcomes

Companies that use CSL Vifor

Customer profile

Named customers2 records

Segments2 records

Ideal customer profiles1 record

CSL Vifor technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature2 records

CSL Vifor partnerships and signals

Strategic signal

Partnerships

Seven partnerships are on record, tiered core and regional.

  • Pfizer, Inc.coreOEM/ Whitelabel/ Licensing Partner · 1 January 2018Licensed Retacrit (Epoetin Alfa-epbx) from Pfizer, approved in the USA since 2018 for all indications of its reference drug, epoetin alfa.
  • F. Hoffmann-La Roche AGcoreOEM/ Whitelabel/ Licensing Partner · 1 January 2015Licensed Mircera (long-acting erythropoiesis-stimulating agent) from Roche since 2015. The product is currently supplied to over 6,500 dialysis clinics in the USA and its territories.
  • Vifor Fresenius Medical Care Renal PharmacoreStrategic or Co-development PartnerJoint company partnership for nephrology products. Together with Vifor Fresenius Medical Care Renal Pharma, CSL Vifor has a strong and rapidly growing presence in nephrology, committed to launching the next generation of therapies to address the full spectrum of kidney disease.
  • Kissei PharmaceuticalregionalChannel Partner/ Reseller/ DistributorKissei distributes Tavneos (Avacopan) in Japan for treatment of ANCA-associated vasculitis.
  • Otsuka PharmaceuticalregionalChannel Partner/ Reseller/ DistributorOtsuka distributes Tavneos in Canada and Korsuva (Difelikefalin) in Canada.
  • CTS (Corporate Technology Solutions)regionalChannel Partner/ Reseller/ DistributorCTS distributes Korsuva (Difelikefalin) in Israel as part of the Middle East partnership.
  • World Federation of Hemophilia (WFH)coreStrategic or Co-development PartnerCSL has long participated in the WFH Humanitarian Aid Program to bring needed medicines to underserved parts of the world. CSL is also proud to support the WFH Path to Access to Care and Treatment (PACT) Program to advance diagnosis, enhance training and advocacy to improve national care. This aligns with CSL's commitment to improve access and equity for patients.

Scale indicators6 records

Recent moves7 records

Expansion highlights5 records

CSL Vifor competitors and assessment

Company assessment

Broad incumbents

  • GSK: Global pharma with rare disease, vaccines, and specialty therapeutics franchises overlapping with CSL Vifor's nephrology and iron deficiency focus. Comparable as a broad incumbent across specialty pharma distribution channels.
  • Pfizer: Licensor of Retacrit (epoetin alfa biosimilar) to CSL Vifor and a global biopharmaceutical incumbent with significant nephrology and biosimilars portfolio. Comparable as a counterparty in CSL Vifor's licensing strategy and as a broad peer in renal anemia.
  • Roche: Originator of Mircera (licensed to CSL Vifor) and a major nephrology and biologics player. Comparable as the licensor of a core CSL Vifor product and as a broader specialty pharma incumbent in nephrology.
  • Amgen: Large biotech with established ESA franchise (Epogen/Aranesp) in the same nephrology anemia market CSL Vifor addresses via Mircera and Retacrit. Comparable as a specialty pharma incumbent in iron/ESA-adjacent nephrology therapeutics.
  • Novartis: Major pharma with specialty and rare disease franchises, including cardiovascular and nephrology adjacencies. Comparable as a broad incumbent competing for the same specialist prescriber audience in CKD and heart failure.
  • Sanofi: Global pharma with rare disease and specialty therapeutics overlap to CSL Vifor's nephrology portfolio. Comparable as a broad incumbent with product adjacencies in iron deficiency and rare renal indications; co-founding supporter of WFH humanitarian programs.

Emerging players

  • Akebia Therapeutics: U.S. biopharma focused on HIF-PHI inhibitors (vadadustat) for anemia in CKD, directly competing with CSL Vifor's ESA/iron franchise. Comparable as an emerging nephrology specialist targeting the same patient population.
  • Ardelyx: Developer of tenapanor and other renal/cardio-renal therapies, with overlap in nephrology patient segments addressed by Veltassa and Velphoro. Comparable as a focused emerging player in CKD complications.

Direct peers

  • Vifor Fresenius Medical Care Renal Pharma: Joint venture between CSL Vifor and Fresenius Medical Care focused exclusively on nephrology products. Comparable as the closest direct peer in nephrology since it shares CSL Vifor's portfolio strategy and channel access.
  • Fresenius Medical Care: World's largest dialysis services and products company and CSL Vifor's joint venture partner in Vifor Fresenius Medical Care Renal Pharma. Closely comparable given shared nephrology focus, shared commercial channel into U.S. dialysis clinics, and overlapping patient populations.

Market position

Strengths4 records

Weaknesses5 records

Competitive moat5 records

Key risks6 records

Key highlights7 records

Customer concentration

CSL Vifor social profiles

Digital presence

CSL Vifor financial estimates

Financial estimate

Revenue estimate

Valuation estimate

CSL Vifor leadership team

Management profile

Number of profiles

CSL Vifor subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

CSL Vifor funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

CSL Vifor 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 CSL Vifor

What does CSL Vifor do?

CSL Vifor develops, manufactures and markets prescription pharmaceutical products for iron deficiency and iron deficiency anaemia across heart failure, kidney disease, gastroenterology, inflammatory bowel disease, patient blood management and women's health, as well as nephrology therapies covering the full spectrum of kidney disease. The company distributes these products globally, supplemented by in-licensed assets and a joint nephrology venture with Fresenius Medical Care.

Is CSL Vifor a public or private company?

CSL Vifor is a public company. It is classified as corporate owned and is currently operating.

When was CSL Vifor founded?

CSL Vifor was founded in 2022. It employs 1,001 to 5,000 people.

Where is CSL Vifor based?

CSL Vifor is headquartered in Glattbrugg, Switzerland, in the Europe region.

How does CSL Vifor make money?

Two revenue lines are on record. Pharmaceutical Product Sales are the primary driver. The others are licensing Royalties.

Who are CSL Vifor's main competitors?

Broad incumbents on record are GSK, Pfizer, Roche, Amgen, Novartis and Sanofi. Emerging players are Akebia Therapeutics and Ardelyx. Direct peers are Vifor Fresenius Medical Care Renal Pharma and Fresenius Medical Care.

Does CSL Vifor have an API?

No public API is recorded for CSL Vifor.

What industry is CSL Vifor in?

CSL Vifor's product category is Specialty Pharmaceuticals — Iron Deficiency and Nephrology. Its primary akta.pro industry code is HLAIACAG, Cardiology & Vascular Specialty Pharmaceuticals. Its SIC code is 2834.

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FiercePharmaTavneos trial flagged for 'serious breaches' of protocol as EU regulators dissect market withdrawal decisionThe European Commission revoked the marketing authorization for Tavneos, an autoimmune disorder treatment owned by CSL Vifor and developed by Amgen, following findings of serious protocol breaches in its pivotal clinical trial. Regulators determined that study personnel improperly accessed unblinded data to alter results, rendering the evidence of efficacy unreliable and outweighing safety concerns regarding liver injury. While Amgen disputes the decision and continues to defend the drug's value in the U.S., the EU market withdrawal is now final.Pharmaceutical TechnologyEMA backs market rollback of rare disease drug Tavneos over data concerns - Pharmaceutical TechnologyThe European Medicines Agency recommended revoking Tavneos' marketing authorisation after its CHMP found the pivotal Advocate study breached good clinical practice. The data was deemed misleading, so benefits no longer outweigh risks, and no new patients should start treatment. The decision follows a similar FDA move and 20 deaths in Japan.pharmaphorumEMA advisors say CSL's Tavneos should be pulled from saleThe EMA's human medicine committee recommended revoking Tavneos approval, following the FDA's data-integrity concerns. CSL Vifor has stopped new patient initiations in EMA jurisdictions. The drug, developed by ChemoCentryx and acquired by Amgen for $3.7 billion, generated $459 million in global sales last year.KalkineCan CSL (ASX:CSL) Overcome Its Revenue Challenges and Return to Growth?CSL Ltd completed its interim CEO's 90-day review and lowered its FY26 revenue guidance to approximately $15.2 billion, citing U.S. immunoglobulin inventory normalization, weaker albumin pricing in China, Middle East geopolitical disruptions, slower HEMGENIX growth, and increased competition in iron therapies. Despite the reduced outlook, CSL shares rose 2.83% as investors responded positively to management's strategic initiatives, operational efficiency measures, and confidence in returning to sustainable profitable growth. The company also announced approximately $5 billion in additional non-cash pre-tax impairments across FY26 and FY27, primarily related to CSL Vifor intangible assets and under-utilized equipment.YahooTravere (TVTX) Q2 2025 Earnings TranscriptTravere Therapeutics reported strong Q2 2025 performance driven by FILSPARI, delivering its strongest commercial quarter for IgA nephropathy with growing physician adoption as foundational therapy. The company expects pipeline and access milestones by year-end including potential modification of liver monitoring REMS and removal of pregnancy testing REMS. The sNDA review for a second indication in FSGS is advancing as expected, while international partners CSL Vifor and Renalis continue expanding FILSPARI access outside the U.S.The Times of IndiaCompetition law vs patent rights: NCLAT rules CCI has no power to probe patented product disputes; upholds case against Swiss drugmaker Vifor - The Times of IndiaThe NCLAT ruled that the Competition Commission of India (CCI) cannot investigate disputes related to patented products, as the Patent Act takes precedence over the Competition Act. This decision upheld the closure of a case against Swiss pharma company Vifor International, which held a patent for a drug used to treat Iron Deficiency Anaemia. The tribunal emphasized the importance of patent rights over competition regulation in such matters.PR NewswireCSL Vifor and Travere Therapeutics Recognize Updated KDIGO Clinical Practice Guidelines for IgA NephropathyCSL Vifor and Travere Therapeutics announced support for the updated KDIGO 2025 clinical practice guidelines for IgA Nephropathy, which now recommend FILSPARI (sparsentan) as a potential first-line approach for patients at risk of progressive kidney function loss. The updated guidelines cite FILSPARI as the only therapy with proven efficacy versus optimized RASi, supported by the PROTECT Phase 3 trial showing a 49.8% mean reduction in proteinuria versus 15.1% for irbesartan. FILSPARI is approved and launched in the US, Germany, Austria, Switzerland, Luxembourg, and the UK, with CSL Vifor holding exclusive commercialization rights in Europe and other territories.PR NewswireCSL Vifor and Travere Therapeutics Recognize Updated KDIGO Clinical Practice Guidelines for IgA NephropathyCSL Vifor and Travere Therapeutics announced their support for the updated KDIGO 2025 clinical practice guidelines for IgA Nephropathy treatment, which recommend FILSPARI (sparsentan) as a potential first-line approach for patients at risk of progressive kidney function loss. The guidelines highlight FILSPARI as the only therapy with proven efficacy compared to optimized RASi therapy, citing PROTECT study data showing 49.8% mean proteinuria reduction versus 15.1% for irbesartan-treated patients. CSL Vifor holds exclusive commercialization rights for FILSPARI in Europe, Australia, New Zealand and other territories, while Travere developed the drug which is approved and launched in the US and several European markets.GlobeNewswireTravere Therapeutics and CSL Vifor Announce Swissmedic Approval of FILSPARI® (sparsentan) for the Treatment of IgA NephropathySwissmedic granted temporary marketing authorization for FILSPARI (sparsentan) to treat adults with IgA nephropathy, based on Phase 3 PROTECT trial results. The approval follows U.S. FDA full approval and EMA conditional authorization, with the company expecting Swiss patients to gain access soon.GlobeNewswireTravere Therapeutics and CSL Vifor Announce European Commission Approves FILSPARI® (sparsentan) for the treatment of IgA NephropathyThe European Commission granted conditional marketing authorization for FILSPARI (sparsentan) for IgA nephropathy, the first non-immunosuppressive therapy for the condition. The approval is based on the PROTECT Study, where sparsentan reduced proteinuria by 49.8% versus 15.1% for irbesartan. CSL Vifor expects launch in European markets in the second half of 2024.