Developer docs
API playgroundTry for free, no card

Search company profiles

Recordati Rare Diseases

Full company profile

uuid000a536

Namestring
Recordati Rare Diseases
Legal namestring
Recordati AG, Rare Diseases Branch
Company typeenum
Public
Founded yearint
1926
Descriptiontext

Recordati Rare Diseases is a specialty pharmaceutical business unit within the publicly traded Recordati S.p.A. group (XMIL: REC), dedicated to developing, manufacturing, and commercialising orphan drugs for rare diseases across three core therapeutic franchises: endocrinology (Cushing's syndrome, acromegaly — including Isturisa and Signifor LAR), oncology-hematology (Castleman disease via Sylvant, cold agglutinin disease via Enjaymo, neuroblastoma via Qarziba, cutaneous T-cell lymphoma via Ledaga), and metabolic disorders (cystinosis, homocystinuria, Wilson's disease, hyperammonemia, phenylketonuria, acute hepatic porphyrias). The unit originated from Recordati's 2007 acquisition of Orphan Europe and was further expanded via the 2022 acquisition of EUSA Pharma and the 2024 acquisition of global rights to Enjaymo from Sanofi. It serves patients and healthcare professionals across approximately 150 countries, distributing through a dedicated 1,600 sq. m. specialist packaging and distribution centre in Paris that handles over 27,000 orders annually to 60+ countries, complemented by hospital pharmacies, specialty pharmacy networks, and direct country operations in the US, Canada, Brazil, Mexico, Colombia, Japan, China, South Korea, Australia, and across Europe.

The business model is anchored in pharmaceutical product sales (one-time licensing of in-house and acquired products) supplemented by licensing and supply agreements (e.g., Vazkepa from Amarin, 2025). Pricing is managed through national health technology assessment bodies and hospital/specialty pharmacy channels rather than direct list pricing, reflecting the orphan-drug reimbursement environment. Go-to-market combines enterprise field sales (highly trained Orphan Drug Specialists engaging healthcare professionals, payers, and regulators across the full patient-management lifecycle) with direct-to-patient advocacy through partnerships with more than a dozen patient organisations including Global Genes, NUCDF, CORD, MetabERN, and Acromegaly Canada. Competitive advantages rest on regulatory expertise in orphan drug designations and named-patient programs, dedicated rare-disease logistics infrastructure, and a 100-year parent-group brand heritage. The Paris distribution centre, combined with the manufacturing footprint of the broader Recordati Group (two chemical plants and seven manufacturing sites worldwide), provides capital-intensive operational depth that smaller competitors cannot easily replicate.

Short descriptiontext

Recordati Rare Diseases is a specialty pharmaceutical business unit within publicly traded Recordati S.p.A. (XMIL: REC) that develops, manufactures, and distributes orphan drugs across endocrinology, oncology-hematology, and metabolic rare disease franchises to patients and healthcare professionals in approximately 150 countries worldwide.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
251–500
akta.pro rankint
HeadquartersMilan, Italy
HQ citystring
Milan
HQ countrystring
Italy
HQ regionstring
Europe
Markets served

Serves global market

Offices4 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
orphan drug pharmaceuticals, rare disease treatments, specialty pharmaceuticals, endocrinology oncology metabolic therapies, biopharmaceutical manufacturing
Industry4 codes
1Rare Oncology & Hematologic Malignancy Therapies
CodeHLAIAIACPrimaryYes
2Rare Endocrine & Growth Disorder Therapies
CodeHLAIAIAJPrimaryNo
3Rare Immunology, Autoimmune & Autoinflammatory Therapies
CodeHLAIAIAEPrimaryNo
4Genetic & Genomic Rare Disease Therapeutics
CodeHLAIAIAAPrimaryNo
NAICS code2 codes
  • Pharmaceutical and Medicine Manufacturing3254
  • Biological Product (except Diagnostic) Manufacturing325414
SIC code2 codes
  • Pharmaceutical Preparations2834
  • Biological Products, (No Disgnostic Substances)2836
Product category
Rare Disease Pharmaceuticals
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model2 records
1Pharmaceutical product sales
TypeOne Time License
Description

Sale of specialty and orphan drugs for rare diseases including treatments for endocrinology, oncology-hematology, and metabolic conditions. Products are distributed globally to hospitals, specialty pharmacies, and directly to patients.

recordatirarediseases.com
2Licensing and supply agreements
TypeLicensing Royalties
Description

Acquisition and licensing of global rights to treatments. Recent agreements include Enjaymo from Sanofi (2024) and Vazkepa from Amarin (2025)

recordatirarediseases.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 components5 values
Technology or R&D, Supply Chain, Operations, Marketing or Sales, Personnel
Pricing details1 tier
1Orphan drug specialty pharmaceuticals
ModelOtherBilling cadenceMulti-year contract
Notes

Pricing managed through HTA bodies, hospital pharmacies, and specialty distribution channels. Market reports indicate hospital pharmacies led distribution channels at 44.80% for carglumic acid market.

recordatirarediseases.com
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Recordati Rare Diseases develops, manufactures, and commercializes pharmaceutical products (orphan drugs) for the treatment of rare diseases. Its portfolio spans three core therapeutic areas—endocrinology, oncology-hematology, and metabolic disorders—and includes more than 20 branded specialty medicines (e.g., Sylvant, Isturisa, Signifor, Cystagon, Carbaglu, Enjaymo) sold globally to hospitals, specialty pharmacies, and through named-patient programs across roughly 60 countries.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • Presence in ~150 countries serving rare disease patients globally
+2 more records
Product overview1 text field

Recordati Rare Diseases is a pharmaceutical company specializing in orphan and rare disease medicines. The company operates a portfolio of specialty pharmaceutical products organized across three core therapeutic areas: Endocrinology (including Cushing's syndrome and acromegaly treatments like ISTURISA and SIGNIFOR), Oncology-Hematology (including treatments for Castleman disease, cold agglutinin disease, cutaneous T-cell lymphoma, neuroblastoma, and rare cancers), and Metabolic disorders (including treatments for cystinosis, homocystinuria, acute hepatic porphyrias, hyperammonemia, Wilson's disease, and phenylketonuria). The product portfolio includes both internally developed and acquired brands commercialized across approximately 60 countries worldwide.

Product and service1 record
1CARBAGLU (carglumic acid)
Scale indicator6 records

Each record includes

Type, Value, Description, Source

Partnership13 partners
Strategic tierCoreTypeOthers
Description

Leading rare disease advocacy organization whose mission is to build awareness, educate the global community, and provide critical connections and resources that equip advocates to become activists for their disease. Recordati provides support and engagement through this partnership.

Strategic tierCoreTypeOthers
Description

Dedicated to the identification, treatment and cure of urea cycle disorders. Partnership supports patient education and awareness for hyperammonemia and related metabolic conditions.

Strategic tierCoreTypeOthers
Description

Canada's national network for organizations representing all those with rare disorders. CORD provides strong common voice to advocate for health policy and healthcare system that works for rare disease patients.

Strategic tierMinorTypeOthers
Description

Canadian permanent national body for coordination of management of inherited metabolic disorders.

5International Porphyria Network
Strategic tierCoreTypeOthers
Description

Worldwide network providing support and information for patients with porphyria and their families, supporting acute hepatic porphyria treatment awareness.

recordatirarediseases.com
Strategic tierCoreTypeOthers
Description

Patient organization network supporting nephropathic cystinosis awareness and treatment access across Europe.

7E-HOD (European Network for Homocystinurias)
Strategic tierMinorTypeOthers
Description

European Network and Registry for Homocystinurias and Methylation Defects supporting diagnosis and treatment awareness.

recordatirarediseases.com
Strategic tierCoreTypeOthers
Description

European Reference Network for Hereditary Metabolic Disorders supporting rare metabolic disease communities.

Strategic tierMinorTypeOthers
Description

Not-for-profit organization established in 2019 to bring together Canadians whose lives touched by acromegaly, raising awareness through education and providing support network.

Strategic tierMinorTypeOthers
Description

Community organization helping people talk about and cope with lymphoma, the fifth most common cancer in Canada.

Strategic tierCoreTypeOthers
Description

Not-for-profit corporate foundation operating independently from business, organizing training on rare diseases to improve diagnosis and spread therapeutic knowledge. Has delivered over 75 courses to over 3,000 healthcare professionals.

12Arrigo Prize
Strategic tierMinorTypeOthers
Description

International recognition prize established in 2000 in memory of Arrigo Recordati to promote scientific research, currently dedicated to paediatric oncology (sarcomas).

recordatirarediseases.com
13Scientific societies partnerships
Strategic tierCoreTypeStrategic or Co-development Partner
Description

Strong and unique partnership with international scientific societies supporting rare disease research, education, and treatment advancement.

recordatirarediseases.com
Recent move12 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Global pharmaceutical company with established rare disease unit (Genzyme) in rare hematology, lysosomal storage disorders, and oncology. Recently divested Enjaymo to Recordati; ongoing competitor in adjacent rare hematology indications.

TypeDirect peer
Description

Pure-play rare disease unit within AstraZeneca specializing in hematology, neurology, and metabolic disorders. Competes head-to-head with Recordati Rare Diseases in cold agglutinin disease (Enjaymo vs. Alexion assets) and similar ultra-rare hematology indications.

TypeRegional player
Description

Italian-headquartered specialty pharmaceutical company with rare disease focus (Chiesi Global Rare Diseases). Geographic overlap in EMEA and comparable therapeutic mix in inherited metabolic disorders. Multiple Recordati Rare Diseases leaders previously held roles at Chiesi.

TypeBroad incumbent
Description

Global pharmaceutical major with multiple rare disease assets across hematology and oncology. Senior Recordati Rare Diseases leadership previously held roles at Novartis Oncology, indicating direct talent overlap and competitive landscape.

TypeBroad incumbent
Description

Global biotechnology company with rare disease presence including hematology and metabolic franchises. Recently partnered with Recordati Rare Diseases via Vazkepa licensing deal (2025), reflecting both competitive and partnering dynamics.

TypeDirect peer
Description

Rare disease-focused commercial-stage company with strong cystic fibrosis franchise overlapping with Recordati Rare Diseases' metabolic portfolio (VEDROP for cystic fibrosis-related vitamin E deficiency).

TypeDirect peer
Description

Dedicated rare disease pharmaceutical company with overlapping focus in hematology, immunology, and specialty metabolic conditions. Most directly comparable European orphan-drug peer with similar go-to-market model and patient-centric distribution approach.

TypeBroad incumbent
Description

Global pharmaceutical major with substantial rare disease franchise following Shire acquisition. Competes in hereditary angioedema, rare hematology, and metabolic diseases; larger portfolio and broader commercial reach than Recordati Rare Diseases.

TypeDirect peer
Description

Clinical and commercial rare disease company developing and commercializing therapies for rare and ultra-rare genetic diseases — directly comparable patient populations and regulatory pathways.

TypeDirect peer
Description

Specialty biotech focused exclusively on rare diseases across endocrinology, hematology, and inherited metabolic disorders. Highly comparable therapeutic mix and reliance on orphan drug exclusivity economics.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 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

Segment3 records

Each record includes

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

Ideal customer profile4 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
Profiles13 records

Each record includes

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

Subsidiaries2 records

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 →

Recordati Rare Diseases

Rare Disease Pharmaceuticalsrecordatirarediseases.com

Recordati Rare Diseases is a specialty pharmaceutical business unit within publicly traded Recordati S.p.A. (XMIL: REC) that develops, manufactures, and distributes orphan drugs across endocrinology, oncology-hematology, and metabolic rare disease franchises to patients and healthcare professionals in approximately 150 countries worldwide.

What Recordati Rare Diseases does

Recordati Rare Diseases is a specialty pharmaceutical business unit within the publicly traded Recordati S.p.A. group (XMIL: REC), dedicated to developing, manufacturing, and commercialising orphan drugs for rare diseases across three core therapeutic franchises: endocrinology (Cushing's syndrome, acromegaly — including Isturisa and Signifor LAR), oncology-hematology (Castleman disease via Sylvant, cold agglutinin disease via Enjaymo, neuroblastoma via Qarziba, cutaneous T-cell lymphoma via Ledaga), and metabolic disorders (cystinosis, homocystinuria, Wilson's disease, hyperammonemia, phenylketonuria, acute hepatic porphyrias). The unit originated from Recordati's 2007 acquisition of Orphan Europe and was further expanded via the 2022 acquisition of EUSA Pharma and the 2024 acquisition of global rights to Enjaymo from Sanofi. It serves patients and healthcare professionals across approximately 150 countries, distributing through a dedicated 1,600 sq. m. specialist packaging and distribution centre in Paris that handles over 27,000 orders annually to 60+ countries, complemented by hospital pharmacies, specialty pharmacy networks, and direct country operations in the US, Canada, Brazil, Mexico, Colombia, Japan, China, South Korea, Australia, and across Europe.

The business model is anchored in pharmaceutical product sales (one-time licensing of in-house and acquired products) supplemented by licensing and supply agreements (e.g., Vazkepa from Amarin, 2025). Pricing is managed through national health technology assessment bodies and hospital/specialty pharmacy channels rather than direct list pricing, reflecting the orphan-drug reimbursement environment. Go-to-market combines enterprise field sales (highly trained Orphan Drug Specialists engaging healthcare professionals, payers, and regulators across the full patient-management lifecycle) with direct-to-patient advocacy through partnerships with more than a dozen patient organisations including Global Genes, NUCDF, CORD, MetabERN, and Acromegaly Canada. Competitive advantages rest on regulatory expertise in orphan drug designations and named-patient programs, dedicated rare-disease logistics infrastructure, and a 100-year parent-group brand heritage. The Paris distribution centre, combined with the manufacturing footprint of the broader Recordati Group (two chemical plants and seven manufacturing sites worldwide), provides capital-intensive operational depth that smaller competitors cannot easily replicate.

Recordati Rare Diseases firmographics

Firmographics
Name
Recordati Rare Diseases
Legal name
Recordati AG, Rare Diseases Branch
Website
https://recordatirarediseases.com
Company type
Public
Founded year
1926
Operating status
Operating
Headcount range
251–500 employees
Short description
Recordati Rare Diseases is a specialty pharmaceutical business unit within publicly traded Recordati S.p.A. (XMIL: REC) that develops, manufactures, and distributes orphan drugs across endocrinology, oncology-hematology, and metabolic rare disease franchises to patients and healthcare professionals in approximately 150 countries worldwide.
Ownership category
akta.pro rank

Recordati Rare Diseases industry classification

Industry
Product category
Rare Disease Pharmaceuticals
NAICS
Pharmaceutical and Medicine Manufacturing (3254), Biological Product (except Diagnostic) Manufacturing (325414)
SIC
Pharmaceutical Preparations (2834), Biological Products, (No Disgnostic Substances) (2836)
akta.pro primary industry
Rare Oncology & Hematologic Malignancy Therapies (HLAIAIAC)
akta.pro secondary industries
Rare Endocrine & Growth Disorder Therapies (HLAIAIAJ), Rare Immunology, Autoimmune & Autoinflammatory Therapies (HLAIAIAE), Genetic & Genomic Rare Disease Therapeutics (HLAIAIAA)

Keywords

  • Orphan drug pharmaceuticals
  • Rare disease treatments
  • Specialty pharmaceuticals
  • Endocrinology oncology metabolic therapies
  • Biopharmaceutical manufacturing

Where Recordati Rare Diseases is headquartered

Location

Headquarters

HQ city
Milan
HQ country
Italy
HQ region
Europe

Offices4 records

Markets served

Recordati Rare Diseases business model

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

Revenue model

  1. Pharmaceutical product sales: Sale of specialty and orphan drugs for rare diseases including treatments for endocrinology, oncology-hematology, and metabolic conditions. Products are distributed globally to hospitals, specialty pharmacies, and directly to patients.
  2. Licensing and supply agreements: Acquisition and licensing of global rights to treatments. Recent agreements include Enjaymo from Sanofi (2024) and Vazkepa from Amarin (2025)

Pricing tiers

ModelBillingPrice
OtherMulti-year contractOrphan drug specialty pharmaceuticals

Go-to-market motion2 records

Distribution channels4 records

Marketing channels5 records

Recordati Rare Diseases product offering

Product offering

Core offering

Recordati Rare Diseases develops, manufactures, and commercializes pharmaceutical products (orphan drugs) for the treatment of rare diseases. Its portfolio spans three core therapeutic areas—endocrinology, oncology-hematology, and metabolic disorders—and includes more than 20 branded specialty medicines (e.g., Sylvant, Isturisa, Signifor, Cystagon, Carbaglu, Enjaymo) sold globally to hospitals, specialty pharmacies, and through named-patient programs across roughly 60 countries.

Product overview

Recordati Rare Diseases is a pharmaceutical company specializing in orphan and rare disease medicines. The company operates a portfolio of specialty pharmaceutical products organized across three core therapeutic areas: Endocrinology (including Cushing's syndrome and acromegaly treatments like ISTURISA and SIGNIFOR), Oncology-Hematology (including treatments for Castleman disease, cold agglutinin disease, cutaneous T-cell lymphoma, neuroblastoma, and rare cancers), and Metabolic disorders (including treatments for cystinosis, homocystinuria, acute hepatic porphyrias, hyperammonemia, Wilson's disease, and phenylketonuria). The product portfolio includes both internally developed and acquired brands commercialized across approximately 60 countries worldwide.

Differentiator

Problem solved

Functional benefit

Products and services

  • CARBAGLU (carglumic acid)

Quantifiable outcome

  • Presence in ~150 countries serving rare disease patients globally
  • +2 more outcomes

Companies that use Recordati Rare Diseases

Customer profile

Named customers2 records

Segments3 records

Ideal customer profiles4 records

Recordati Rare Diseases technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

Recordati Rare Diseases partnerships and signals

Strategic signal

Partnerships

13 partnerships are on record, tiered core and minor.

  • Global GenescoreOthersLeading rare disease advocacy organization whose mission is to build awareness, educate the global community, and provide critical connections and resources that equip advocates to become activists for their disease. Recordati provides support and engagement through this partnership.
  • National Urea Cycle Disorders Foundation (NUCDF)coreOthersDedicated to the identification, treatment and cure of urea cycle disorders. Partnership supports patient education and awareness for hyperammonemia and related metabolic conditions.
  • Canadian Organization for Rare Disorders (CORD)coreOthersCanada's national network for organizations representing all those with rare disorders. CORD provides strong common voice to advocate for health policy and healthcare system that works for rare disease patients.
  • The Garrod AssociationminorOthersCanadian permanent national body for coordination of management of inherited metabolic disorders.
  • International Porphyria NetworkcoreOthersWorldwide network providing support and information for patients with porphyria and their families, supporting acute hepatic porphyria treatment awareness.
  • Cystinosis Network EuropecoreOthersPatient organization network supporting nephropathic cystinosis awareness and treatment access across Europe.
  • E-HOD (European Network for Homocystinurias)minorOthersEuropean Network and Registry for Homocystinurias and Methylation Defects supporting diagnosis and treatment awareness.
  • MetabERN (European Reference Network)coreOthersEuropean Reference Network for Hereditary Metabolic Disorders supporting rare metabolic disease communities.
  • Acromegaly CanadaminorOthersNot-for-profit organization established in 2019 to bring together Canadians whose lives touched by acromegaly, raising awareness through education and providing support network.
  • Lymphoma CanadaminorOthersCommunity organization helping people talk about and cope with lymphoma, the fifth most common cancer in Canada.
  • Recordati Rare Diseases FoundationcoreOthersNot-for-profit corporate foundation operating independently from business, organizing training on rare diseases to improve diagnosis and spread therapeutic knowledge. Has delivered over 75 courses to over 3,000 healthcare professionals.
  • Arrigo PrizeminorOthersInternational recognition prize established in 2000 in memory of Arrigo Recordati to promote scientific research, currently dedicated to paediatric oncology (sarcomas).
  • Scientific societies partnershipscoreStrategic or Co-development PartnerStrong and unique partnership with international scientific societies supporting rare disease research, education, and treatment advancement.

Scale indicators6 records

Recent moves12 records

Expansion highlights6 records

Recordati Rare Diseases competitors and assessment

Company assessment

Broad incumbents

  • Sanofi (Genzyme Rare Diseases): Global pharmaceutical company with established rare disease unit (Genzyme) in rare hematology, lysosomal storage disorders, and oncology. Recently divested Enjaymo to Recordati; ongoing competitor in adjacent rare hematology indications.
  • Novartis (Rare Disease franchises): Global pharmaceutical major with multiple rare disease assets across hematology and oncology. Senior Recordati Rare Diseases leadership previously held roles at Novartis Oncology, indicating direct talent overlap and competitive landscape.
  • Amgen: Global biotechnology company with rare disease presence including hematology and metabolic franchises. Recently partnered with Recordati Rare Diseases via Vazkepa licensing deal (2025), reflecting both competitive and partnering dynamics.
  • Takeda (Shire Rare Disease): Global pharmaceutical major with substantial rare disease franchise following Shire acquisition. Competes in hereditary angioedema, rare hematology, and metabolic diseases; larger portfolio and broader commercial reach than Recordati Rare Diseases.

Direct peers

  • Alexion (AstraZeneca Rare Disease): Pure-play rare disease unit within AstraZeneca specializing in hematology, neurology, and metabolic disorders. Competes head-to-head with Recordati Rare Diseases in cold agglutinin disease (Enjaymo vs. Alexion assets) and similar ultra-rare hematology indications.
  • Vertex Pharmaceuticals: Rare disease-focused commercial-stage company with strong cystic fibrosis franchise overlapping with Recordati Rare Diseases' metabolic portfolio (VEDROP for cystic fibrosis-related vitamin E deficiency).
  • Sobi (Swedish Orphan Biovitrum): Dedicated rare disease pharmaceutical company with overlapping focus in hematology, immunology, and specialty metabolic conditions. Most directly comparable European orphan-drug peer with similar go-to-market model and patient-centric distribution approach.
  • Ultragenyx Pharmaceutical: Clinical and commercial rare disease company developing and commercializing therapies for rare and ultra-rare genetic diseases — directly comparable patient populations and regulatory pathways.
  • BioMarin Pharmaceutical: Specialty biotech focused exclusively on rare diseases across endocrinology, hematology, and inherited metabolic disorders. Highly comparable therapeutic mix and reliance on orphan drug exclusivity economics.

Regional players

  • Chiesi Farmaceutici: Italian-headquartered specialty pharmaceutical company with rare disease focus (Chiesi Global Rare Diseases). Geographic overlap in EMEA and comparable therapeutic mix in inherited metabolic disorders. Multiple Recordati Rare Diseases leaders previously held roles at Chiesi.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat5 records

Key risks6 records

Key highlights7 records

Customer concentration

Recordati Rare Diseases social profiles

Digital presence

Recordati Rare Diseases financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Recordati Rare Diseases leadership team

Management profile

Number of profiles

Profiles13 records

Recordati Rare Diseases subsidiaries and ownership

Company hierarchy

Subsidiaries2 records

Recordati Rare Diseases funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

Recordati Rare Diseases 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 Recordati Rare Diseases

What does Recordati Rare Diseases do?

Recordati Rare Diseases develops, manufactures, and commercializes pharmaceutical products (orphan drugs) for the treatment of rare diseases. Its portfolio spans three core therapeutic areas—endocrinology, oncology-hematology, and metabolic disorders—and includes more than 20 branded specialty medicines (e.g., Sylvant, Isturisa, Signifor, Cystagon, Carbaglu, Enjaymo) sold globally to hospitals, specialty pharmacies, and through named-patient programs across roughly 60 countries.

Is Recordati Rare Diseases a public or private company?

Recordati Rare Diseases is a public company. It is classified as corporate owned and is currently operating.

When was Recordati Rare Diseases founded?

Recordati Rare Diseases was founded in 1926. It employs 251 to 500 people.

Where is Recordati Rare Diseases based?

Recordati Rare Diseases is headquartered in Milan, Italy, in the Europe region.

How does Recordati Rare Diseases make money?

Two revenue lines are on record. Pharmaceutical product sales are the primary driver. The others are licensing and supply agreements.

Who are Recordati Rare Diseases's main competitors?

Broad incumbents on record are Sanofi (Genzyme Rare Diseases), Novartis (Rare Disease franchises), Amgen and Takeda (Shire Rare Disease). Direct peers are Alexion (AstraZeneca Rare Disease), Vertex Pharmaceuticals, Sobi (Swedish Orphan Biovitrum), Ultragenyx Pharmaceutical and BioMarin Pharmaceutical. Chiesi Farmaceutici is listed as a regional player.

Does Recordati Rare Diseases have an API?

No public API is recorded for Recordati Rare Diseases.

What industry is Recordati Rare Diseases in?

Recordati Rare Diseases's product category is Rare Disease Pharmaceuticals. Its primary akta.pro industry code is HLAIAIAC, Rare Oncology & Hematologic Malignancy Therapies, with a secondary code of HLAIAIAJ, Rare Endocrine & Growth Disorder Therapies. Its NAICS code is 3254 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
Mexico Business NewsThe Critical Role of Multidisciplinary Care in Rare DiseasesMultidisciplinary care is essential for rare diseases, which affect 300 million people and often require coordinated specialists. Examples include mucopolysaccharidoses, Gaucher disease, and Fabry disease, where team-based management improves outcomes. The article notes Mexico faces challenges in specialist availability and fragmented care.GlobeNewswireSylvant (Siltuximab: Recordati Rare Diseases) Market Research Report 2026: Increasing Adoption of Targeted Il-6 Inhibitor Therapies and Growing Use in Rare Immunological Disorders - Forecast to 2035ResearchAndMarkets.com published a market research report on the Sylvant (siltuximab) market projecting growth through 2035, driven by increased diagnosis of multicentric Castleman disease (MCD), improved awareness of cytokine-driven disorders, and advances in monoclonal antibody development. The report notes that in 2024 the European Commission approved Sylvant for treating MCD, while North America dominated the market in 2025 with Asia-Pacific projected to grow rapidly. The analysis identifies key trends including targeted IL-6 inhibitor therapies, expanded use in rare immunological disorders, and precision medicine approaches leveraging patient-specific genetic data.PR NewswireRecordati Rare Diseases Showcases Real-World Evidence Studies That Advance Understanding of Castleman Disease (CD) at the American Society of Hematology (ASH) Annual MeetingRecordati Rare Diseases announced the presentation of four new studies on Castleman disease at the 67th American Society of Hematology Annual Meeting in Orlando. The research highlighted an AI-driven histopathology grading model, a real-world analysis showing significantly higher morbidity and healthcare costs for idiopathic multicentric CD patients, and data on pediatric disease severity and treatment response to siltuximab. These findings aim to advance the understanding and diagnosis of this rare immune system disorder.PR NewswireRecordati Rare Diseases to Share New Data at the American Society of Hematology (ASH) MeetingRecordati Rare Diseases Inc. announced it will present nine poster presentations at the 67th American Society of Hematology Annual Meeting in Orlando, Florida, December 6-9, 2025, highlighting advances in treatments for rare hematologic disorders including Castleman disease, cold agglutinin disease, and CAR T-cell therapy complications. The presentations will feature research on an AI model for Castleman disease diagnosis, real-world safety data for sutimlimab, and evaluations of siltuximab for cytokine release syndrome. The data showcase Recordati's ongoing commitment to advancing care for rare hematologic conditions, with presentations including both company-sponsored and independent investigator-sponsored studies.PR NewswireRECORDATI RARE DISEASES ANNOUNCES PUBLICATION OF LONG-TERM OUTCOMES FROM THE EXTENSION TO THE PHASE III LINC 3 STUDY OF ISTURISA® (OSILODROSTAT) IN PATIENTS WITH CUSHING'S DISEASE IN THE EUROPEAN JOURRecordati Rare Diseases Inc. announced the publication of long-term outcomes from the open-label extension phase of the Phase III LINC 3 study of ISTURISA (osilodrostat) in The European Journal of Endocrinology, with 106 of 113 patients completing the extension receiving continued treatment for a median duration of 130 weeks. Key findings showed sustained efficacy, with 81.1% of patients maintaining mean urinary free cortisol at or below the upper limit of normal at week 72, alongside maintained or improved cardiovascular, metabolic, and quality-of-life parameters. The drug was generally well tolerated with no unexpected adverse events reported during the extension phase.PR NewswireRecordati Rare Diseases Announces Availability of CYSTADROPS® (Cysteamine Ophthalmic Solution) 0.37% in the U.S.Recordati Rare Diseases Inc. announced that CYSTADROPS (cysteamine ophthalmic solution) 0.37% is now available for prescription and distribution across the United States, providing a new treatment option for corneal cystine crystal deposits in patients with cystinosis. The drug is the first and only FDA-approved cysteamine eye drop formulation with four-times-daily dosing, supported by clinical trial data showing a 40 percent reduction in corneal crystal density at 90 days and a 30 percent decrease maintained over a five-year period. CYSTADROPS is available exclusively through Anovo specialty pharmacy, which will provide patient support services including insurance benefit investigations and financial aid resources.PR NewswireU.S. FDA Approves CYSTADROPS® (Cysteamine Ophthalmic Solution) 0.37%, A New Practical Treatment Option for the Ocular Manifestations of CystinosisThe U.S. Food and Drug Administration has approved CYSTADROPS® (cysteamine ophthalmic solution) 0.37%, a new viscous eye drop treatment for corneal cystine crystal deposits in patients with cystinosis, developed by Recordati Rare Diseases Inc. Clinical trials demonstrated a 40% reduction in corneal crystal density at 90 days and a sustained 30% reduction over five years, with the product offering practical four-times-daily dosing as the first and only FDA-approved cysteamine eye drop formulation. The approval addresses a significant unmet need for the approximately 600 cystinosis patients in the U.S. who previously faced limited practical treatment options for ocular manifestations of the rare genetic disorder.GlobeNewswireRecordati Rare Diseases now holds Isturisa® European MARecordati Rare Diseases became the European Marketing Authorization holder of Isturisa (osilodrostat) for adult patients with Cushing's syndrome, covering all EU member states plus the UK, Norway, Iceland, and Liechtenstein. The company expects commercialization to begin in Q3 2020.PR NewswireRecordati: Isturisa® (Osilodrostat) Approved In The U.S.Recordati Rare Diseases Inc. announced that the U.S. FDA has approved Isturisa (osilodrostat) for the treatment of patients with Cushing's disease who are not candidates for or have failed pituitary surgery. The approval grants the drug orphan status, providing seven years of market exclusivity, and confirms its efficacy in normalizing cortisol levels in a significant portion of adult patients. Recordati expects the therapy to become commercially available in the U.S. during the second or third quarter of 2020.PR NewswireRecordati Rare Diseases, Inc. Announces Transfer of U.S. Marketing Rights to SIGNIFOR® (pasireotide) Injection and SIGNIFOR LAR® (pasireotide) for Injectable SuspensionRecordati Rare Diseases, Inc. announced the transfer of U.S. marketing rights for SIGNIFOR (pasireotide) injection and SIGNIFOR LAR (pasireotide) injectable suspension, two FDA-approved medications for Cushing's disease and acromegaly. The products will be marketed through Recordati Rare Diseases' newly established Endocrinology franchise with uninterrupted supply to patients and healthcare providers. Both medications are somatostatin analogs indicated for rare endocrine disorders where pituitary surgery is not an option or has not been curative.