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Averoa

Full company profile

uuid002lkoy

Namestring
Averoa
Legal namestring
AVEROA SAS
Company typeenum
Private
Founded yearint
2021
Descriptiontext

Averoa is a privately held French biopharmaceutical company incorporated as AVEROA SAS, founded in December 2021 in Meylan (Grenoble), France, to develop and commercialize therapies for unmet needs in nephrology. The company's lead product, XOANACYL® (AVA1014, Ferric Citrate Coordination Complex), is an oral therapy approved by the European Commission in June 2025 and by the UK MHRA in October 2025 for the concomitant treatment of iron deficiency anaemia and hyperphosphatemia in adult chronic kidney disease (CKD) patients. The asset was in-licensed from Akebia Therapeutics in December 2022 (where it is already marketed as Auryxia in the US and Riona in Japan) and Averoa holds exclusive development and commercialization rights for Europe, UK, Switzerland, and Turkey.

The portfolio is being expanded through the LUCIOL project, a research collaboration with IDIBELL, CIBER, and the University of Barcelona focused on renal lithiasis and cystinuria. The pipeline comprises AVA2206, a natural thiolhistidine antioxidant in late preclinical development for cystinuria, which has received Orphan Drug Designation from both the EMA and US FDA, and AVA2065, a companion diagnostic biomarker validated in preclinical models. Intellectual property includes registered trademarks (XOANACYL®, AVEROA) and formulation patents held by senior staff (four patents, three granted in EU, US, and Japan, held by the COO; two additional formulation patents by the Pharmaceutical Development Manager).

The business model combines in-licensing of late-stage assets with strong therapeutic and commercial fit, internal development leveraging regulatory expertise (including repositioning in new indications and pursuing orphan designation), and a planned network of commercial partners and distributors across licensed territories. The go-to-market targets European, UK, Swiss, and Turkish markets for XOANACYL®, with revenue mechanics based on product sales through this partner network. Averoa operates with a lean team of 1-10 employees and is led by an experienced management group including Dr. Luc-André Granier (President & CEO; co-founder of Advicenne and Panntherapi and the lead on the duloxetine/Cymbalta FDA approval in 2004), Sarah Delbaere (CFO; supported Advicenne's IPO on Euronext), Caroline Roussel-Maupetit (COO), Scott Donald (Business Development Director), and senior regulatory and clinical advisors. Share capital is stated at €1,329,799; no institutional funding rounds, revenue figures, or ownership structure beyond founder control are publicly disclosed.

Short descriptiontext

Averoa is a private French biopharmaceutical company developing therapies for renal diseases, including XOANACYL® (approved in the EU and UK for iron deficiency anaemia and hyperphosphatemia in CKD) and a pipeline of orphan-designated candidates for cystinuria and renal lithiasis.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersMeylan, France
HQ citystring
Meylan
HQ countrystring
France
HQ regionstring
Europe
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
renal disease therapeutics, chronic kidney disease, biopharmaceutical products, renal lithiasis treatment, prescription pharmaceuticals
Industry2 codes
1Nephrology & Urology Specialty Pharmaceuticals
CodeHLAIACAHPrimaryYes
2Rare Renal & Nephrology Disorder Therapies
CodeHLAIAIAIPrimaryNo
NAICS code2 codes
  • Pharmaceutical and Medicine Manufacturing3254
  • Scientific Research and Development Services5417
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Renal Therapeutics / Nephrology Pharmaceuticals
Social media profiles1 record
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model2 records
1Product Sales - XOANACYL
TypeOne Time License
Description

Sales of FDA/EMA approved oral therapy XOANACYL (Ferric Citrate) for chronic kidney disease patients with iron deficiency and hyperphosphatemia. Licensed from Akebia Therapeutics and already marketed in US (Auryxia) and Japan (Riona).

averoa-pharma.org
2Licensing and Commercialization Rights
TypeLicensing Royalties
Description

Averoa develops and commercializes in-licensed products in Europe, UK, Switzerland, and Turkey. The company builds portfolio through in-licensing late-stage drugs and develops network of commercial partners and distributors.

averoa-pharma.org
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 components4 values
Personnel, Technology or R&D, Operations, Marketing or Sales
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 3 records shown
1XOANACYL® (AVA1014)
Description

Ferric Citrate Coordination Complex - oral therapy for treating iron deficiency and elevated serum phosphorus in CKD patients. Received European Marketing Authorisation on June 11, 2025 and UK MHRA Marketing Authorisation on October 30, 2025.

averoa-pharma.org
+2 more records
Core offering1 text field

Averoa is a biopharmaceutical company that develops and commercializes prescription therapeutics for renal diseases. Its lead product XOANACYL (Ferric Citrate Coordination Complex) is an oral therapy approved in the EU and UK for treating iron deficiency anemia and hyperphosphatemia in adult chronic kidney disease (CKD) patients. The pipeline includes AVA2206 (Orphan Drug Designation from EMA and FDA) and AVA2065 (companion diagnostic biomarker) for renal lithiasis and cystinuria under the LUCIOL project.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 2 values shown
  • 50% recurrence rate at 5 years without intervention for renal lithiasis
+1 more record
Product overview1 text field

Averoa is a biopharmaceutical company dedicated to developing innovative medicines for nephrology. Their portfolio consists of XOANACYL® (AVA1014), an approved oral therapy for iron deficiency anemia and hyperphosphatemia in CKD patients, and the LUCIOL project pipeline featuring AVA2206 (a novel antioxidant treatment for renal lithiasis in late preclinical stage with Orphan Drug Designation) paired with AVA2065 (a companion biomarker diagnostic for cystinuria). The approved product and pipeline candidates address distinct therapeutic areas within renal diseases.

Product and service3 records
1XOANACYL (AVA1014)
CategoryPrescription pharmaceutical (CKD therapeutics)
Description

XOANACYL (Ferric Citrate Coordination Complex) is an oral therapy for treating iron deficiency anemia and elevated serum phosphorus (hyperphosphatemia) in adult patients with Chronic Kidney Disease (CKD). It is the only treatment approved in Europe and the UK for these concomitant complications in adult CKD patients.

2AVA2206
CategoryPipeline pharmaceutical (renal lithiasis therapeutics)
Description

AVA2206 is a natural thiolhistidine antioxidant in late preclinical development for treating renal lithiasis, specifically cystinuria. It targets the early process of crystallization to prevent stone formation and has received Orphan Drug Designation from both the EMA and US FDA.

3AVA2065
CategoryCompanion diagnostic (renal lithiasis biomarker)
Description

AVA2065 is a preclinical cystine lithiasis biomarker designed as a companion diagnostic test to predict stone formation and assess treatment response in cystinuria patients.

Scale indicator6 records

Each record includes

Type, Value, Description, Source

Partnership4 partners
Strategic tierCoreTypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2022-12-01
Description

Exclusive Licence agreement granting AVEROA rights to develop and commercialize AVA1014 (XOANACYL) in Europe, UK, Switzerland and Turkey. The product was licensed in December 2022. AVA1014 is already registered and marketed in the US under the brand name Auryxia and in Japan under Riona. Averoa revised the clinical package and regulatory strategy for European market needs, supported by 3 pivotal clinical studies performed by Keryx Biopharmaceuticals (a wholly owned subsidiary of Akebia).

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Research collaboration and license agreement for development of a biomarker (AVA2065) and new treatment (AVA2206) for renal lithiasis. Collaboration also involves CIBER and University of Barcelona for development and exploitation in the field of kidney and/or metabolic diseases.

Strategic tierSecondaryTypeStrategic or Co-development Partner
Description

Collaboration partner alongside IDIBELL and University of Barcelona for the LUCIOL project developing AVA2206 and AVA2065 for renal lithiasis treatment and diagnosis.

Strategic tierSecondaryTypeStrategic or Co-development Partner
Description

Academic research partner in the LUCIOL project for development of AVA2206 treatment and AVA2065 biomarker for renal lithiasis in collaboration with IDIBELL and CIBER.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeEmerging player
Description

Ardelyx commercializes tenapanor (Xphozah) for hyperphosphatemia in CKD patients on dialysis in the US. It is a focused emerging player in the same hyperphosphatemia indication that XOANACYL addresses, providing a benchmark for nephrology-focused commercial execution.

TypeBroad incumbent
Description

Belgian-Dutch biopharmaceutical company with historical focus on inflammation and fibrotic diseases including renal indications. While broader in scope, it provides a relevant European mid-cap benchmark for specialty pharma commercial strategy and capital markets positioning.

TypeBroad incumbent
Description

Dutch specialty pharma company commercializing treatments for rare diseases including renal and immunological conditions. It is a relevant European listed comparable for a small-cap specialty pharma scaling through European commercial infrastructure.

TypeDirect peer
Description

Shield Therapeutics developed ferric maltol (Accrufer/Feraccru), an oral iron therapy targeting iron deficiency. It shares Averoa's oral iron deficiency therapeutic angle and European commercialization focus, making it a directly comparable specialty pharma peer in adjacent nephrology/iron markets.

TypeDirect peer
Description

French specialty pharma company founded by Averoa CEO Dr Luc-André Granier, focused on rare renal diseases and nephrology therapeutics including treatments for distal renal tubular acidosis. It is a direct peer sharing founder DNA, therapeutic focus on nephrology, and European commercialization orientation.

TypeEmerging player
Description

Chinook Therapeutics was a clinical-stage nephrology company developing treatments for rare kidney diseases (atrasentan, zigakibart) before its acquisition by Novartis in 2023. It represents a strategic exit benchmark for focused rare renal disease biotechs similar to Averoa's pipeline ambitions.

TypeBroad incumbent
Description

Vifor Pharma is a global leader in iron deficiency and nephrology, with products such as Ferinject/Injectafer (IV iron) and a broad renal portfolio. It is a broad incumbent in Averoa's therapeutic categories and represents the dominant established competitor in CKD iron deficiency management across Europe.

TypeEmerging player
Description

Travere Therapeutics is a rare disease-focused biopharmaceutical company with sparsentan (FILSPARI) approved for IgA nephropathy, a rare kidney disease. It is an emerging player in rare renal therapeutics with comparable orphan-drug commercialization strategies.

TypeOthers
Description

While focused on RNAi therapeutics rather than nephrology, Dicerna was acquired by Novo Nordisk in 2021 and represents a strategic acquirer profile that has historically targeted renal and rare disease biotech assets, making it relevant for understanding potential exit pathways for Averoa.

TypeDirect peer
Description

Akebia developed and markets ferric citrate (Auryxia) in the US for CKD patients with iron deficiency anemia and hyperphosphatemia. It is Averoa's licensor and the originator of XOANACYL, making it the most directly comparable peer with an overlapping product in the same indication.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 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

Segment3 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

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles7 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 →

Averoa

Renal Therapeutics / Nephrology Pharmaceuticalsaveroa-pharma.org

Averoa is a private French biopharmaceutical company developing therapies for renal diseases, including XOANACYL® (approved in the EU and UK for iron deficiency anaemia and hyperphosphatemia in CKD) and a pipeline of orphan-designated candidates for cystinuria and renal lithiasis.

What Averoa does

Averoa is a privately held French biopharmaceutical company incorporated as AVEROA SAS, founded in December 2021 in Meylan (Grenoble), France, to develop and commercialize therapies for unmet needs in nephrology. The company's lead product, XOANACYL® (AVA1014, Ferric Citrate Coordination Complex), is an oral therapy approved by the European Commission in June 2025 and by the UK MHRA in October 2025 for the concomitant treatment of iron deficiency anaemia and hyperphosphatemia in adult chronic kidney disease (CKD) patients. The asset was in-licensed from Akebia Therapeutics in December 2022 (where it is already marketed as Auryxia in the US and Riona in Japan) and Averoa holds exclusive development and commercialization rights for Europe, UK, Switzerland, and Turkey.

The portfolio is being expanded through the LUCIOL project, a research collaboration with IDIBELL, CIBER, and the University of Barcelona focused on renal lithiasis and cystinuria. The pipeline comprises AVA2206, a natural thiolhistidine antioxidant in late preclinical development for cystinuria, which has received Orphan Drug Designation from both the EMA and US FDA, and AVA2065, a companion diagnostic biomarker validated in preclinical models. Intellectual property includes registered trademarks (XOANACYL®, AVEROA) and formulation patents held by senior staff (four patents, three granted in EU, US, and Japan, held by the COO; two additional formulation patents by the Pharmaceutical Development Manager).

The business model combines in-licensing of late-stage assets with strong therapeutic and commercial fit, internal development leveraging regulatory expertise (including repositioning in new indications and pursuing orphan designation), and a planned network of commercial partners and distributors across licensed territories. The go-to-market targets European, UK, Swiss, and Turkish markets for XOANACYL®, with revenue mechanics based on product sales through this partner network. Averoa operates with a lean team of 1-10 employees and is led by an experienced management group including Dr. Luc-André Granier (President & CEO; co-founder of Advicenne and Panntherapi and the lead on the duloxetine/Cymbalta FDA approval in 2004), Sarah Delbaere (CFO; supported Advicenne's IPO on Euronext), Caroline Roussel-Maupetit (COO), Scott Donald (Business Development Director), and senior regulatory and clinical advisors. Share capital is stated at €1,329,799; no institutional funding rounds, revenue figures, or ownership structure beyond founder control are publicly disclosed.

Averoa firmographics

Firmographics
Name
Averoa
Legal name
AVEROA SAS
Website
https://averoa-pharma.org
Company type
Private
Founded year
2021
Operating status
Operating
Headcount range
1–10 employees
Short description
Averoa is a private French biopharmaceutical company developing therapies for renal diseases, including XOANACYL® (approved in the EU and UK for iron deficiency anaemia and hyperphosphatemia in CKD) and a pipeline of orphan-designated candidates for cystinuria and renal lithiasis.
Ownership category
akta.pro rank

Averoa industry classification

Industry
Product category
Renal Therapeutics / Nephrology Pharmaceuticals
NAICS
Pharmaceutical and Medicine Manufacturing (3254), Scientific Research and Development Services (5417)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
Nephrology & Urology Specialty Pharmaceuticals (HLAIACAH)
akta.pro secondary industry
Rare Renal & Nephrology Disorder Therapies (HLAIAIAI)

Keywords

  • Renal disease therapeutics
  • Chronic kidney disease
  • Biopharmaceutical products
  • Renal lithiasis treatment
  • Prescription pharmaceuticals

Where Averoa is headquartered

Location

Headquarters

HQ city
Meylan
HQ country
France
HQ region
Europe

Offices2 records

Markets served

Averoa business model

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

Revenue model

  1. Product Sales - XOANACYL: Sales of FDA/EMA approved oral therapy XOANACYL (Ferric Citrate) for chronic kidney disease patients with iron deficiency and hyperphosphatemia. Licensed from Akebia Therapeutics and already marketed in US (Auryxia) and Japan (Riona).
  2. Licensing and Commercialization Rights: Averoa develops and commercializes in-licensed products in Europe, UK, Switzerland, and Turkey. The company builds portfolio through in-licensing late-stage drugs and develops network of commercial partners and distributors.

Go-to-market motion2 records

Distribution channels1 record

Marketing channels3 records

Averoa product offering

Product offering

Core offering

Averoa is a biopharmaceutical company that develops and commercializes prescription therapeutics for renal diseases. Its lead product XOANACYL (Ferric Citrate Coordination Complex) is an oral therapy approved in the EU and UK for treating iron deficiency anemia and hyperphosphatemia in adult chronic kidney disease (CKD) patients. The pipeline includes AVA2206 (Orphan Drug Designation from EMA and FDA) and AVA2065 (companion diagnostic biomarker) for renal lithiasis and cystinuria under the LUCIOL project.

Product overview

Averoa is a biopharmaceutical company dedicated to developing innovative medicines for nephrology. Their portfolio consists of XOANACYL® (AVA1014), an approved oral therapy for iron deficiency anemia and hyperphosphatemia in CKD patients, and the LUCIOL project pipeline featuring AVA2206 (a novel antioxidant treatment for renal lithiasis in late preclinical stage with Orphan Drug Designation) paired with AVA2065 (a companion biomarker diagnostic for cystinuria). The approved product and pipeline candidates address distinct therapeutic areas within renal diseases.

Differentiator

Problem solved

Functional benefit

Brands

  • XOANACYL® (AVA1014): Ferric Citrate Coordination Complex - oral therapy for treating iron deficiency and elevated serum phosphorus in CKD patients. Received European Marketing Authorisation on June 11, 2025 and UK MHRA Marketing Authorisation on October 30, 2025.
  • AVA2206 (LUCIOL project)
  • AVA2065

Products and services

  • XOANACYL (AVA1014) XOANACYL (Ferric Citrate Coordination Complex) is an oral therapy for treating iron deficiency anemia and elevated serum phosphorus (hyperphosphatemia) in adult patients with Chronic Kidney Disease (CKD). It is the only treatment approved in Europe and the UK for these concomitant complications in adult CKD patients.
  • AVA2206 AVA2206 is a natural thiolhistidine antioxidant in late preclinical development for treating renal lithiasis, specifically cystinuria. It targets the early process of crystallization to prevent stone formation and has received Orphan Drug Designation from both the EMA and US FDA.
  • AVA2065 AVA2065 is a preclinical cystine lithiasis biomarker designed as a companion diagnostic test to predict stone formation and assess treatment response in cystinuria patients.

Quantifiable outcome

  • 50% recurrence rate at 5 years without intervention for renal lithiasis
  • +1 more outcomes

Companies that use Averoa

Customer profile

Segments3 records

Ideal customer profiles2 records

Averoa technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

Averoa partnerships and signals

Strategic signal

Partnerships

Four partnerships are on record, tiered core and secondary.

  • Akebia Therapeutics, Inc. (AKBA)coreOEM/ Whitelabel/ Licensing Partner · 1 December 2022Exclusive Licence agreement granting AVEROA rights to develop and commercialize AVA1014 (XOANACYL) in Europe, UK, Switzerland and Turkey. The product was licensed in December 2022. AVA1014 is already registered and marketed in the US under the brand name Auryxia and in Japan under Riona. Averoa revised the clinical package and regulatory strategy for European market needs, supported by 3 pivotal clinical studies performed by Keryx Biopharmaceuticals (a wholly owned subsidiary of Akebia).
  • IDIBELL (Institut d'Investigació Biomèdica de Bellvitge)coreStrategic or Co-development PartnerResearch collaboration and license agreement for development of a biomarker (AVA2065) and new treatment (AVA2206) for renal lithiasis. Collaboration also involves CIBER and University of Barcelona for development and exploitation in the field of kidney and/or metabolic diseases.
  • CIBER (Biomedical Research Networking Centres)secondaryStrategic or Co-development PartnerCollaboration partner alongside IDIBELL and University of Barcelona for the LUCIOL project developing AVA2206 and AVA2065 for renal lithiasis treatment and diagnosis.
  • University of BarcelonasecondaryStrategic or Co-development PartnerAcademic research partner in the LUCIOL project for development of AVA2206 treatment and AVA2065 biomarker for renal lithiasis in collaboration with IDIBELL and CIBER.

Scale indicators6 records

Recent moves6 records

Expansion highlights5 records

Averoa competitors and assessment

Company assessment

Emerging players

  • Ardelyx: Ardelyx commercializes tenapanor (Xphozah) for hyperphosphatemia in CKD patients on dialysis in the US. It is a focused emerging player in the same hyperphosphatemia indication that XOANACYL addresses, providing a benchmark for nephrology-focused commercial execution.
  • Chinook Therapeutics (acquired by Novartis): Chinook Therapeutics was a clinical-stage nephrology company developing treatments for rare kidney diseases (atrasentan, zigakibart) before its acquisition by Novartis in 2023. It represents a strategic exit benchmark for focused rare renal disease biotechs similar to Averoa's pipeline ambitions.
  • Travere Therapeutics: Travere Therapeutics is a rare disease-focused biopharmaceutical company with sparsentan (FILSPARI) approved for IgA nephropathy, a rare kidney disease. It is an emerging player in rare renal therapeutics with comparable orphan-drug commercialization strategies.

Broad incumbents

  • Galapagos NV: Belgian-Dutch biopharmaceutical company with historical focus on inflammation and fibrotic diseases including renal indications. While broader in scope, it provides a relevant European mid-cap benchmark for specialty pharma commercial strategy and capital markets positioning.
  • Pharming Group: Dutch specialty pharma company commercializing treatments for rare diseases including renal and immunological conditions. It is a relevant European listed comparable for a small-cap specialty pharma scaling through European commercial infrastructure.
  • Vifor Pharma (CSL Vifor): Vifor Pharma is a global leader in iron deficiency and nephrology, with products such as Ferinject/Injectafer (IV iron) and a broad renal portfolio. It is a broad incumbent in Averoa's therapeutic categories and represents the dominant established competitor in CKD iron deficiency management across Europe.

Direct peers

  • Shield Therapeutics: Shield Therapeutics developed ferric maltol (Accrufer/Feraccru), an oral iron therapy targeting iron deficiency. It shares Averoa's oral iron deficiency therapeutic angle and European commercialization focus, making it a directly comparable specialty pharma peer in adjacent nephrology/iron markets.
  • Advicenne: French specialty pharma company founded by Averoa CEO Dr Luc-André Granier, focused on rare renal diseases and nephrology therapeutics including treatments for distal renal tubular acidosis. It is a direct peer sharing founder DNA, therapeutic focus on nephrology, and European commercialization orientation.
  • Akebia Therapeutics: Akebia developed and markets ferric citrate (Auryxia) in the US for CKD patients with iron deficiency anemia and hyperphosphatemia. It is Averoa's licensor and the originator of XOANACYL, making it the most directly comparable peer with an overlapping product in the same indication.

Others

  • Dicerna Pharmaceuticals (acquired by Novo Nordisk): While focused on RNAi therapeutics rather than nephrology, Dicerna was acquired by Novo Nordisk in 2021 and represents a strategic acquirer profile that has historically targeted renal and rare disease biotech assets, making it relevant for understanding potential exit pathways for Averoa.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks7 records

Key highlights7 records

Customer concentration

Averoa social profiles

Digital presence

Averoa financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Averoa leadership team

Management profile

Number of profiles

Profiles7 records

Averoa funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

Averoa 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 Averoa

What does Averoa do?

Averoa is a biopharmaceutical company that develops and commercializes prescription therapeutics for renal diseases. Its lead product XOANACYL (Ferric Citrate Coordination Complex) is an oral therapy approved in the EU and UK for treating iron deficiency anemia and hyperphosphatemia in adult chronic kidney disease (CKD) patients. The pipeline includes AVA2206 (Orphan Drug Designation from EMA and FDA) and AVA2065 (companion diagnostic biomarker) for renal lithiasis and cystinuria under the LUCIOL project.

Is Averoa a public or private company?

Averoa is a private company. It is classified as founder individual operated bootstrapped and is currently operating.

When was Averoa founded?

Averoa was founded in 2021. It employs 1 to 10 people.

Where is Averoa based?

Averoa is headquartered in Meylan, France, in the Europe region.

How does Averoa make money?

Two revenue lines are on record. Product Sales - XOANACYL is the primary driver. The others are licensing and Commercialization Rights.

Who are Averoa's main competitors?

Emerging players on record are Ardelyx, Chinook Therapeutics (acquired by Novartis) and Travere Therapeutics. Broad incumbents are Galapagos NV, Pharming Group and Vifor Pharma (CSL Vifor). Direct peers are Shield Therapeutics, Advicenne and Akebia Therapeutics. Dicerna Pharmaceuticals (acquired by Novo Nordisk) is listed as an others.

Does Averoa have an API?

No public API is recorded for Averoa.

What industry is Averoa in?

Averoa's product category is Renal Therapeutics / Nephrology Pharmaceuticals. Its primary akta.pro industry code is HLAIACAH, Nephrology & Urology Specialty Pharmaceuticals, with a secondary code of HLAIAIAI, Rare Renal & Nephrology Disorder Therapies. Its NAICS code is 3254 and its SIC code is 2834.

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Live signals
GlobeNewswireAVEROA Receives UK MHRA Approval for XOANACYL®, an Oral Therapy Targeting Key Complications of Chronic Kidney Disease (CKD)The UK MHRA granted marketing authorization for XOANACYL, an oral therapy for CKD complications, under the International Recognition Procedure. The drug addresses iron deficiency and elevated serum phosphorus in a single formulation, with over 3 million UK CKD patients and 10 million in Europe. Averoa is now engaging partners to accelerate European market access.GlobeNewswireAVEROA Receives UK MHRA Approval for XOANACYL®, an Oral Therapy Targeting Key Complications of Chronic Kidney Disease (CKD)Averoa received UK MHRA approval for XOANACYL, an oral therapy for CKD complications, after European approval in June 2025. The drug is the only approved treatment in Europe targeting both iron deficiency and elevated serum phosphorus in CKD patients.GlobeNewswireAVEROA receives European marketing authorization for XOANACYL®, an Oral Therapy for Chronic Kidney Disease (CKD)The European Commission granted marketing authorization for Averoa's XOANACYL, an oral therapy for iron deficiency and hyperphosphatemia in chronic kidney disease. The approval follows a positive CHMP opinion and data from three Akebia trials. Averoa has submitted the application to the UK MHRA under the International Recognition Procedure.GlobeNewswireAkebia Therapeutics Announces Positive Opinion of European Medicines Agency for XOANACYL®, an Oral Therapy for Chronic Kidney Disease Licensed to AveroaAkebia Therapeutics announced the EMA's CHMP adopted a positive opinion for XOANACYL, an oral therapy for elevated serum phosphorous and iron deficiency in adult CKD patients. Averoa, which licensed the rights, will have the European Commission review the recommendation, with a final decision expected in about two months.GlobeNewswireAVEROA Receives Positive Opinion from the European Medicines Agency for XOANACYL®, an Oral Therapy for Chronic Kidney Disease (CKD)Averoa received a positive opinion from the EMA's CHMP for XOANACYL, an oral therapy for chronic kidney disease. The final EU approval is expected by June 2025, with a UK submission via MHRA's international recognition procedure. Averoa is seeking strategic commercial partners to bring the therapy to market.GlobeNewswireAVEROA Submits Marketing Authorisation Application to the European Medicines Agency Seeking Approval of AVA1014 for Treating Complications Associated with Chronic Kidney DiseaseAveroa submitted a marketing authorisation application to the EMA for AVA1014, an oral iron-based compound for chronic kidney disease complications. The application is supported by three pivotal clinical studies from Akebia, with a decision expected in 2025 under the centralised procedure.