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Chiesi

Full company profile

uuid0005wf8

Namestring
Chiesi
Legal namestring
Chiesi Limited
Websiteurl
chiesi.uk.com
Company typeenum
Private
Founded yearint
1935
Short descriptiontext

Chiesi is a privately held, family-owned global pharmaceutical group founded in 1935 that develops, manufactures, and commercializes prescription therapies across respiratory health, rare diseases, and specialty care (neonatology and transplantation) across 31 global affiliates and 7 R&D centers.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
251–500
akta.pro rankint
HeadquartersManchester, United Kingdom
HQ citystring
Manchester
HQ countrystring
United Kingdom
HQ regionstring
Europe
Markets served

Serves global market

Offices8 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
respiratory pharmaceuticals, rare disease therapies, neonatal care medicines, inhaled asthma treatments, enzyme replacement therapy
Industry3 codes
1Respiratory & Allergy Pharmaceuticals
CodeHLAIAAAHPrimaryYes
2Pulmonology & Allergy Specialty Pharmaceuticals
CodeHLAIACAFPrimaryNo
3Nebulizers & Aerosol Drug Delivery Systems
CodeHLAHAIAJPrimaryNo
NAICS code2 codes
  • Biological Product (except Diagnostic) Manufacturing325414
  • Medicinal and Botanical Manufacturing325411
SIC code2 codes
  • Biological Products, (No Disgnostic Substances)2836
  • Medicinal Chemicals & Botanical Products2833
Product category
Specialty Pharmaceuticals
Social media profiles2 records
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model2 records
1Pharmaceutical Product Sales
TypeOne Time License
Description

Chiesi generates revenue through development, manufacturing, and sale of prescription pharmaceutical products in respiratory health, rare diseases, and specialty care including neonatology and organ transplantation. Products are sold directly to healthcare systems, hospitals, pharmacies, and through NHS procurement.

fiercepharma.com
2Rare Disease Portfolio Revenue
TypeOne Time License
Description

Revenue from rare disease treatments including Elfabrio ($49 million in 2025 sales), EKTERLY/sebetralstat ($49.1 million in 2025 following US launch), and lomitapide. Strategic goal to reach €6 billion in revenue by 2030.

biospace.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

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

Cost components6 values
Technology or R&D, Personnel, Operations, Supply Chain, Marketing or Sales, Infrastructure
Pricing details1 tier
1Prescription pharmaceutical products - pricing determined through NHS and regulatory negotiations
ModelOtherBilling cadenceMulti-year contract
Notes

Products available through prescription only. NHS pricing negotiated through framework agreements. Patient access programs and support available.

chiesi.uk.com
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 record
1Chiesi Global Rare Diseases
Description

Business unit delivering innovative therapies and solutions for people living with rare diseases including Fabry disease, cystinosis, lipodystrophy, and hereditary angioedema.

chiesi.uk.com
Core offering1 text field

Chiesi develops, manufactures, and commercializes prescription pharmaceutical products across three core therapeutic franchises: Air (respiratory health including asthma and COPD treatments delivered via pMDIs, DPIs, and nebulizers), Rare (therapies for rare and ultra-rare diseases including Fabry disease, HoFH, hereditary angioedema, lipodystrophy, cystinosis, and LHON), and Care (specialty products for neonatology and organ transplantation). The company also operates digital health initiatives including AI-powered vocal biomarker pilots and the Carbon Minimal Inhaler program targeting 90% carbon footprint reduction in respiratory treatments.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 5 values shown
  • Reduces carbon footprint of pMDIs by up to 90% compared to current HFA-134a inhalers
+4 more records
Product overview1 text field

Chiesi is a research-oriented international biopharmaceutical group with a diversified portfolio organized around three core disease areas: Air (respiratory health including asthma and COPD), Rare (rare and ultra-rare diseases), and Care (specialty care including neonatology and organ transplantation). The company operates both a core pharmaceutical portfolio and a dedicated Chiesi Global Rare Diseases business unit. The respiratory portfolio includes inhaled therapies delivered via multiple device formats: pMDI inhalers (Clenil Modulite, Fostair pMDI, Trimbow pMDI), dry powder inhalers (Fostair NEXThaler, Trimbow NEXThaler, Atimos Modulite), and nebulized antibiotics (Bramitob, Quinsair). The rare disease portfolio spans enzyme replacement therapies (Elfabrio for Fabry disease, Lamzede for alpha-mannosidosis), oral therapies (LOJUXTA for HoFH, Myalepta for lipodystrophy, Procysbi for cystinosis, Raxone for LHON), and acquired products (EKTERLY for hereditary angioedema). Specialty care includes neonatal products (Curosurf surfactant, Peyona caffeine), transplant immunosuppression (Envarsus tacrolimus), and supporting therapies across cardiovascular, hematology, and dermatology. Chiesi also operates digital health initiatives including the Carbon Minimal Inhaler program targeting 90% carbon footprint reduction, Salesforce-based commercial operations platforms, and AI-powered diagnostic technologies.

Product and service24 records
1Clenil Modulite
CategoryRespiratory pharmaceuticals
Description

Pressurized metered dose inhaler (pMDI) containing beclometasone in 50mcg, 100mcg, 200mcg, and 250mcg strengths for asthma management. Chiesi's first carbon minimal inhaler candidate, with the HFA-152a formulation submitted to MHRA targeting up to 90% carbon footprint reduction.

2Fostair NEXThaler
CategoryRespiratory pharmaceuticals
Description

Dry powder inhaler combining beclometasone and formoterol in 100/6 and 200/6 dose strengths for asthma and COPD management.

3Fostair pMDI
CategoryRespiratory pharmaceuticals
Description

Pressurized metered dose inhaler combining beclometasone and formoterol in 100/6 and 200/6 dose strengths for respiratory disease treatment.

4Trimbow
CategoryRespiratory pharmaceuticals
Description

Triple combination therapy inhaler containing beclometasone, formoterol, and glycopyrronium available in multiple strengths and delivery formats (NEXThaler DPI and pMDI) for COPD management.

5Atimos Modulite
CategoryRespiratory pharmaceuticals
Description

Breath-actuated breath-coordinated modulit inhaler containing formoterol as a long-acting bronchodilator for asthma and COPD.

6Elfabrio (pegunigalsidase alfa)
CategoryRare disease enzyme replacement therapy
Description

PEGylated enzyme replacement therapy for adult patients with Fabry disease. Plant cell culture-expressed recombinant alpha-galactosidase A enzyme with stabilized pharmacokinetics. Approved with standard 1mg/kg every-two-weeks dosing and additional 2mg/kg every-four-weeks regimen for ERT-stable patients, reducing infusion frequency from 26 to 13 annually.

7LOJUXTA (lomitapide)
CategoryRare disease lipid-lowering therapy
Description

Microsomal triglyceride transfer protein inhibitor for Homozygous Familial Hypercholesterolaemia (HoFH). Originally approved for adults in 2013, with European Commission approval extended in June 2026 to include children 5 years and older.

8Myalepta (metreleptin)
CategoryRare disease metabolic therapy
Description

Recombinant human leptin analog for treatment of lipodystrophy. Chiesi Global Rare Diseases presented metreleptin research at ENDO 2026 across generalized and partial lipodystrophy, including combination therapy with GLP-1 receptor agonists.

9EKTERLY (sebetralstat)
CategoryRare disease oral therapy
Description

First and only oral, on-demand plasma kallikrein inhibitor for acute hereditary angioedema (HAE) attacks in patients 12 years and older. Acquired through Chiesi's $1.9 billion acquisition of KalVista Pharmaceuticals in June 2026. Approved in US, UK, EU, Japan, Australia, Switzerland, and Singapore. Generated $49 million in 2025 sales.

10Lamzede (velmanase alfa)
CategoryRare disease enzyme replacement therapy
Description

Recombinant human alpha-mannosidase enzyme replacement therapy for alpha-mannosidosis, a rare lysosomal storage disorder.

11Procysbi (mercaptamine bitartrate)
CategoryRare disease metabolic therapy
Description

Delayed-release cysteamine bitartrate formulation for nephropathic cystinosis, reducing cystine accumulation in lysosomes.

12Raxone (idebenone)
CategoryRare disease ophthalmology therapy
Description

Synthetic short-chain coenzyme Q10 analog for Leber hereditary optic neuropathy (LHON). Received Complete Response Letter from FDA regarding New Drug Application.

13Curosurf (poractant alfa)
CategoryNeonatal care pharmaceutical
Description

Natural porcine pulmonary surfactant for treatment of respiratory distress syndrome in premature infants.

14Peyona (caffeine citrate)
CategoryNeonatal care pharmaceutical
Description

Caffeine citrate solution for primary apnea of premature newborns.

15Envarsus (tacrolimus monohydrate)
CategoryTransplant immunosuppression therapy
Description

Once-daily tacrolimus formulation for immunosuppression in kidney and liver transplant recipients.

16Bramitob (tobramycin)
CategoryCystic fibrosis inhaled antibiotic
Description

Inhaled tobramycin solution for Pseudomonas aeruginosa infection management in cystic fibrosis patients.

17Quinsair (levofloxacin)
CategoryCystic fibrosis inhaled antibiotic
Description

Inhaled levofloxacin for chronic Pseudomonas aeruginosa lung infections in cystic fibrosis patients.

18Ferriprox (deferiprone)
CategoryHematology iron chelation therapy
Description

Oral iron chelator for treatment of iron overload in thalassemia and other transfusion-dependent anemias.

19Filsuvez Gel
CategoryRare disease dermatology therapy
Description

Topical gel containing birch bark extract for junctional and dystrophic epidermolysis bullosa.

20Kengrexal (cangrelor)
CategoryCardiovascular pharmaceutical
Description

Intravenous P2Y12 platelet receptor antagonist for percutaneous coronary intervention.

21Cardioplen XL (felodipine)
CategoryCardiovascular pharmaceutical
Description

Extended-release calcium channel blocker for hypertension and angina in 2.5mg, 5mg, and 10mg strengths.

22Monomax XL (isosorbide mononitrate)
CategoryCardiovascular pharmaceutical
Description

Extended-release nitrate for prevention of angina pectoris.

23Clipper (budesonide)
CategoryGastroenterology pharmaceutical
Description

Budesonide formulation for inflammatory bowel conditions.

24Natecal D3
CategoryNutritional supplement
Description

Calcium carbonate and cholecalciferol combination for calcium deficiency.

Scale indicator9 records

Each record includes

Type, Value, Description, Source

Partnership8 partners
Strategic tierCoreTypeOthersAnnounced on2026-04-29
Description

Acquisition completed June 11, 2026 for $1.9 billion ($27 per share), making KalVista a wholly owned subsidiary. Acquisition adds EKTERLY (sebetralstat), first oral on-demand treatment for hereditary angioedema, to Chiesi's rare disease portfolio. Approximately 77.8% of shares tendered.

Strategic tierMajorTypeTechnology or IntegrationAnnounced on2026-04-20
Description

Chiesi selected Salesforce Agentforce Life Sciences platform to transform commercial operations, serving 3,300 users with unified data management through Data 360, AI-assisted field team support, and scalable commercial operations management. Partnership supports digital transformation amid geopolitical, regulatory, and supply chain pressures.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-03-18
Description

£10 million Respiratory Transformation Partnership co-funded by NHS England and four pharmaceutical companies (AstraZeneca, Chiesi, GSK, Sanofi) to transform asthma and COPD care by shifting treatment from hospitals to local communities. Partnership uses data and digital tools to improve diagnosis and expand access to biologic medicines.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-03-11
Description

Expanded partnership to increase pMDI manufacturing capacity at Bespak's Holmes Chapel site supporting Chiesi's Carbon Minimal Inhaler program. Partnership aims to reduce carbon footprint of pMDIs by up to 90% through transition to low GWP propellants. Reinforces both companies' sustainability commitments with Chiesi targeting Net Zero by 2035 and Bespak holding SBTi-validated decarbonization targets.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Global partnership for development and commercialization of pegunigalsidase alfa (Elfabrio) for Fabry disease. Chiesi received $25 million milestone payment following EC approval of E4W dosing regimen. Protalix manufactures using proprietary plant cell-based expression system ProCellEx.

Strategic tierMinorTypeStrategic or Co-development Partner
Description

Six-month clinical pilot with Rome-based digital health startup to explore AI-powered vocal biomarker technology for early detection of COPD and chronic respiratory diseases via smartphone voice recordings.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Global collaboration with Gossamer Bio for joint development of seralutinib in pulmonary arterial hypertension. Phase 3 PROSERA study completed with +13.3m improvement in Six-Minute Walk Distance at Week 24. Discussions with FDA ongoing for potential NDA submission.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Multiple collaborative working projects with NHS trusts including Manchester University NHS Foundation Trust (PIONEER post-transplant project), Hull University Teaching Hospitals (FRONTIER COPD diagnosis), Wirral Primary Care Collaborative (COMET), Health Innovation Manchester (MISSION), and Academic Health Science Network (NTEC neonatal project).

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight7 records

Each record includes

Type, Description

Market position
Competitive moat5 records

Each record includes

Type, Details

Key risks1 record

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers3 records

Each record includes

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

Segment4 records

Each record includes

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

Ideal customer profile3 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 capability2 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles12 records

Each record includes

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

Subsidiaries4 records

Each record includes

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

Compliance5 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

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

M&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 →

Chiesi

Specialty Pharmaceuticalschiesi.uk.com

Chiesi is a privately held, family-owned global pharmaceutical group founded in 1935 that develops, manufactures, and commercializes prescription therapies across respiratory health, rare diseases, and specialty care (neonatology and transplantation) across 31 global affiliates and 7 R&D centers.

Chiesi firmographics

Firmographics
Name
Chiesi
Legal name
Chiesi Limited
Website
https://chiesi.uk.com
Company type
Private
Founded year
1935
Operating status
Operating
Headcount range
251–500 employees
Short description
Chiesi is a privately held, family-owned global pharmaceutical group founded in 1935 that develops, manufactures, and commercializes prescription therapies across respiratory health, rare diseases, and specialty care (neonatology and transplantation) across 31 global affiliates and 7 R&D centers.
Ownership category
akta.pro rank

Chiesi industry classification

Industry
Product category
Specialty Pharmaceuticals
NAICS
Biological Product (except Diagnostic) Manufacturing (325414), Medicinal and Botanical Manufacturing (325411)
SIC
Biological Products, (No Disgnostic Substances) (2836), Medicinal Chemicals & Botanical Products (2833)
akta.pro primary industry
Respiratory & Allergy Pharmaceuticals (HLAIAAAH)
akta.pro secondary industries
Pulmonology & Allergy Specialty Pharmaceuticals (HLAIACAF), Nebulizers & Aerosol Drug Delivery Systems (HLAHAIAJ)

Keywords

  • Respiratory pharmaceuticals
  • Rare disease therapies
  • Neonatal care medicines
  • Inhaled asthma treatments
  • Enzyme replacement therapy

Where Chiesi is headquartered

Location

Headquarters

HQ city
Manchester
HQ country
United Kingdom
HQ region
Europe

Offices8 records

Markets served

Chiesi business model

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

Revenue model

  1. Pharmaceutical Product Sales: Chiesi generates revenue through development, manufacturing, and sale of prescription pharmaceutical products in respiratory health, rare diseases, and specialty care including neonatology and organ transplantation. Products are sold directly to healthcare systems, hospitals, pharmacies, and through NHS procurement.
  2. Rare Disease Portfolio Revenue: Revenue from rare disease treatments including Elfabrio ($49 million in 2025 sales), EKTERLY/sebetralstat ($49.1 million in 2025 following US launch), and lomitapide. Strategic goal to reach €6 billion in revenue by 2030.

Pricing tiers

ModelBillingPrice
OtherMulti-year contractPrescription pharmaceutical products - pricing determined through NHS and regulatory negotiations

Go-to-market motion2 records

Distribution channels3 records

Marketing channels5 records

Chiesi product offering

Product offering

Core offering

Chiesi develops, manufactures, and commercializes prescription pharmaceutical products across three core therapeutic franchises: Air (respiratory health including asthma and COPD treatments delivered via pMDIs, DPIs, and nebulizers), Rare (therapies for rare and ultra-rare diseases including Fabry disease, HoFH, hereditary angioedema, lipodystrophy, cystinosis, and LHON), and Care (specialty products for neonatology and organ transplantation). The company also operates digital health initiatives including AI-powered vocal biomarker pilots and the Carbon Minimal Inhaler program targeting 90% carbon footprint reduction in respiratory treatments.

Product overview

Chiesi is a research-oriented international biopharmaceutical group with a diversified portfolio organized around three core disease areas: Air (respiratory health including asthma and COPD), Rare (rare and ultra-rare diseases), and Care (specialty care including neonatology and organ transplantation). The company operates both a core pharmaceutical portfolio and a dedicated Chiesi Global Rare Diseases business unit. The respiratory portfolio includes inhaled therapies delivered via multiple device formats: pMDI inhalers (Clenil Modulite, Fostair pMDI, Trimbow pMDI), dry powder inhalers (Fostair NEXThaler, Trimbow NEXThaler, Atimos Modulite), and nebulized antibiotics (Bramitob, Quinsair). The rare disease portfolio spans enzyme replacement therapies (Elfabrio for Fabry disease, Lamzede for alpha-mannosidosis), oral therapies (LOJUXTA for HoFH, Myalepta for lipodystrophy, Procysbi for cystinosis, Raxone for LHON), and acquired products (EKTERLY for hereditary angioedema). Specialty care includes neonatal products (Curosurf surfactant, Peyona caffeine), transplant immunosuppression (Envarsus tacrolimus), and supporting therapies across cardiovascular, hematology, and dermatology. Chiesi also operates digital health initiatives including the Carbon Minimal Inhaler program targeting 90% carbon footprint reduction, Salesforce-based commercial operations platforms, and AI-powered diagnostic technologies.

Differentiator

Problem solved

Functional benefit

Brands

  • Chiesi Global Rare Diseases: Business unit delivering innovative therapies and solutions for people living with rare diseases including Fabry disease, cystinosis, lipodystrophy, and hereditary angioedema.

Products and services

  • Clenil Modulite Pressurized metered dose inhaler (pMDI) containing beclometasone in 50mcg, 100mcg, 200mcg, and 250mcg strengths for asthma management. Chiesi's first carbon minimal inhaler candidate, with the HFA-152a formulation submitted to MHRA targeting up to 90% carbon footprint reduction.
  • Fostair NEXThaler Dry powder inhaler combining beclometasone and formoterol in 100/6 and 200/6 dose strengths for asthma and COPD management.
  • Fostair pMDI Pressurized metered dose inhaler combining beclometasone and formoterol in 100/6 and 200/6 dose strengths for respiratory disease treatment.
  • Trimbow Triple combination therapy inhaler containing beclometasone, formoterol, and glycopyrronium available in multiple strengths and delivery formats (NEXThaler DPI and pMDI) for COPD management.
  • Atimos Modulite Breath-actuated breath-coordinated modulit inhaler containing formoterol as a long-acting bronchodilator for asthma and COPD.
  • Elfabrio (pegunigalsidase alfa) PEGylated enzyme replacement therapy for adult patients with Fabry disease. Plant cell culture-expressed recombinant alpha-galactosidase A enzyme with stabilized pharmacokinetics. Approved with standard 1mg/kg every-two-weeks dosing and additional 2mg/kg every-four-weeks regimen for ERT-stable patients, reducing infusion frequency from 26 to 13 annually.
  • LOJUXTA (lomitapide) Microsomal triglyceride transfer protein inhibitor for Homozygous Familial Hypercholesterolaemia (HoFH). Originally approved for adults in 2013, with European Commission approval extended in June 2026 to include children 5 years and older.
  • Myalepta (metreleptin) Recombinant human leptin analog for treatment of lipodystrophy. Chiesi Global Rare Diseases presented metreleptin research at ENDO 2026 across generalized and partial lipodystrophy, including combination therapy with GLP-1 receptor agonists.
  • EKTERLY (sebetralstat) First and only oral, on-demand plasma kallikrein inhibitor for acute hereditary angioedema (HAE) attacks in patients 12 years and older. Acquired through Chiesi's $1.9 billion acquisition of KalVista Pharmaceuticals in June 2026. Approved in US, UK, EU, Japan, Australia, Switzerland, and Singapore. Generated $49 million in 2025 sales.
  • Lamzede (velmanase alfa) Recombinant human alpha-mannosidase enzyme replacement therapy for alpha-mannosidosis, a rare lysosomal storage disorder.
  • Procysbi (mercaptamine bitartrate) Delayed-release cysteamine bitartrate formulation for nephropathic cystinosis, reducing cystine accumulation in lysosomes.
  • Raxone (idebenone) Synthetic short-chain coenzyme Q10 analog for Leber hereditary optic neuropathy (LHON). Received Complete Response Letter from FDA regarding New Drug Application.
  • Curosurf (poractant alfa) Natural porcine pulmonary surfactant for treatment of respiratory distress syndrome in premature infants.
  • Peyona (caffeine citrate) Caffeine citrate solution for primary apnea of premature newborns.
  • Envarsus (tacrolimus monohydrate) Once-daily tacrolimus formulation for immunosuppression in kidney and liver transplant recipients.
  • Bramitob (tobramycin) Inhaled tobramycin solution for Pseudomonas aeruginosa infection management in cystic fibrosis patients.
  • Quinsair (levofloxacin) Inhaled levofloxacin for chronic Pseudomonas aeruginosa lung infections in cystic fibrosis patients.
  • Ferriprox (deferiprone) Oral iron chelator for treatment of iron overload in thalassemia and other transfusion-dependent anemias.
  • Filsuvez Gel Topical gel containing birch bark extract for junctional and dystrophic epidermolysis bullosa.
  • Kengrexal (cangrelor) Intravenous P2Y12 platelet receptor antagonist for percutaneous coronary intervention.
  • Cardioplen XL (felodipine) Extended-release calcium channel blocker for hypertension and angina in 2.5mg, 5mg, and 10mg strengths.
  • Monomax XL (isosorbide mononitrate) Extended-release nitrate for prevention of angina pectoris.
  • Clipper (budesonide) Budesonide formulation for inflammatory bowel conditions.
  • Natecal D3 Calcium carbonate and cholecalciferol combination for calcium deficiency.

Quantifiable outcome

  • Reduces carbon footprint of pMDIs by up to 90% compared to current HFA-134a inhalers
  • +4 more outcomes

Companies that use Chiesi

Customer profile

Named customers3 records

Segments4 records

Ideal customer profiles3 records

Chiesi technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

AI capability2 records

Feature3 records

Chiesi partnerships and signals

Strategic signal

Partnerships

Eight partnerships are on record, tiered core, major and minor.

  • KalVista PharmaceuticalscoreOthers · 29 April 2026Acquisition completed June 11, 2026 for $1.9 billion ($27 per share), making KalVista a wholly owned subsidiary. Acquisition adds EKTERLY (sebetralstat), first oral on-demand treatment for hereditary angioedema, to Chiesi's rare disease portfolio. Approximately 77.8% of shares tendered.
  • SalesforcemajorTechnology or Integration · 20 April 2026Chiesi selected Salesforce Agentforce Life Sciences platform to transform commercial operations, serving 3,300 users with unified data management through Data 360, AI-assisted field team support, and scalable commercial operations management. Partnership supports digital transformation amid geopolitical, regulatory, and supply chain pressures.
  • NHS EnglandcoreStrategic or Co-development Partner · 18 March 2026£10 million Respiratory Transformation Partnership co-funded by NHS England and four pharmaceutical companies (AstraZeneca, Chiesi, GSK, Sanofi) to transform asthma and COPD care by shifting treatment from hospitals to local communities. Partnership uses data and digital tools to improve diagnosis and expand access to biologic medicines.
  • BespakcoreStrategic or Co-development Partner · 11 March 2026Expanded partnership to increase pMDI manufacturing capacity at Bespak's Holmes Chapel site supporting Chiesi's Carbon Minimal Inhaler program. Partnership aims to reduce carbon footprint of pMDIs by up to 90% through transition to low GWP propellants. Reinforces both companies' sustainability commitments with Chiesi targeting Net Zero by 2035 and Bespak holding SBTi-validated decarbonization targets.
  • Protalix BioTherapeuticscoreStrategic or Co-development PartnerGlobal partnership for development and commercialization of pegunigalsidase alfa (Elfabrio) for Fabry disease. Chiesi received $25 million milestone payment following EC approval of E4W dosing regimen. Protalix manufactures using proprietary plant cell-based expression system ProCellEx.
  • VoiceMedminorStrategic or Co-development PartnerSix-month clinical pilot with Rome-based digital health startup to explore AI-powered vocal biomarker technology for early detection of COPD and chronic respiratory diseases via smartphone voice recordings.
  • Gossamer BiocoreStrategic or Co-development PartnerGlobal collaboration with Gossamer Bio for joint development of seralutinib in pulmonary arterial hypertension. Phase 3 PROSERA study completed with +13.3m improvement in Six-Minute Walk Distance at Week 24. Discussions with FDA ongoing for potential NDA submission.
  • NHS Trusts (Multiple)coreStrategic or Co-development PartnerMultiple collaborative working projects with NHS trusts including Manchester University NHS Foundation Trust (PIONEER post-transplant project), Hull University Teaching Hospitals (FRONTIER COPD diagnosis), Wirral Primary Care Collaborative (COMET), Health Innovation Manchester (MISSION), and Academic Health Science Network (NTEC neonatal project).

Scale indicators9 records

Recent moves7 records

Expansion highlights7 records

Chiesi competitors and assessment

Company assessment

Market position

Competitive moat5 records

Key risks1 record

Key highlights6 records

Customer concentration

Chiesi social profiles

Digital presence

Chiesi compliance and trust

Trust signal

Compliance5 records

Chiesi financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Chiesi leadership team

Management profile

Number of profiles

Profiles12 records

Chiesi subsidiaries and ownership

Company hierarchy

Subsidiaries4 records

Chiesi funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

Chiesi 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 Chiesi

What does Chiesi do?

Chiesi develops, manufactures, and commercializes prescription pharmaceutical products across three core therapeutic franchises: Air (respiratory health including asthma and COPD treatments delivered via pMDIs, DPIs, and nebulizers), Rare (therapies for rare and ultra-rare diseases including Fabry disease, HoFH, hereditary angioedema, lipodystrophy, cystinosis, and LHON), and Care (specialty products for neonatology and organ transplantation). The company also operates digital health initiatives including AI-powered vocal biomarker pilots and the Carbon Minimal Inhaler program targeting 90% carbon footprint reduction in respiratory treatments.

Is Chiesi a public or private company?

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

When was Chiesi founded?

Chiesi was founded in 1935. It employs 251 to 500 people.

Where is Chiesi based?

Chiesi is headquartered in Manchester, United Kingdom, in the Europe region.

How does Chiesi make money?

Two revenue lines are on record. Pharmaceutical Product Sales are the primary driver. The others are rare Disease Portfolio Revenue.

Does Chiesi have an API?

No public API is recorded for Chiesi.

What industry is Chiesi in?

Chiesi's product category is Specialty Pharmaceuticals. Its primary akta.pro industry code is HLAIAAAH, Respiratory & Allergy Pharmaceuticals, with a secondary code of HLAIACAF, Pulmonology & Allergy Specialty Pharmaceuticals. Its NAICS code is 325414 and its SIC code is 2836.

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FinancialContent Business PageChiesi Group Delivers Solid H1 2026 Performance, Combining Growth, Continued Investment in Innovation and Positive Economic Impact Across CommunitiesChiesi Group reported H1 2026 revenues of €1.89 billion, up 3.6% at constant exchange rates, driven by rare diseases and inhaled triple therapy growth. The company invested €426 million in R&D (22.5% of sales) and completed the KalVista Pharmaceuticals acquisition. Its Economic Footprint study shows €6 billion GDP impact and 56,488 jobs supported.BioSpaceGossamer Bio Announces Second Quarter 2026 Financial Results and Provides Business UpdateGossamer Bio reported Q2 2026 net income of $16.9 million and $57.0 million in cash, with R&D expenses down to $26.4 million. The company plans to submit an NDA for seralutinib in PAH in September 2026 after a productive FDA meeting, and reacquired worldwide rights from Chiesi for a $5 million payment.GlobeNewswirePatient and Dermatologist Raise Awareness of Epidermolysis Bullosa With YourUpdateTVPatient Henry DeAngelis and dermatologist Dr. Lisa Swanson joined Chiesi Global Rare Diseases in a media tour to raise awareness of epidermolysis bullosa (EB). About 200 children are born with EB annually in the U.S., and 3,800 people live with it. Since 2023, several FDA-approved treatments have been available.pharmaphorumUK postcode lottery ends for 'life-changing' cystinosis drugNHS England approved routine commissioning of Chiesi's Procysbi for cystinosis patients in England, ending the postcode lottery. The drug, taken every 12 hours, is more convenient than Cystagon, and about 150 of the UK's 200 diagnosed cases are expected to be eligible. The decision follows over three years of campaigning by patient groups.The Pharma LetterNHS England backs Procysbi for ultra-rare nephropathic cystinosisNHS England has recommended Procysbi (mercaptamine bitartrate gastro-resistant hard capsules) for routine commissioning for eligible patients aged one year and above with nephropathic cystinosis, according to Italian drugmaker Chiesi. The decision grants patients access to a twice-daily cystine-depleting therapy option, offering a more convenient dosing regimen compared to the currently commissioned four-times-daily immediate-release formulation.GossamerbioGossamer Bio Announces FDA Regulatory Update and Reacquisition of Worldwide Rights Related to Seralutinib and Provides a Business UpdateGossamer Bio announced FDA meeting minutes support a September 2026 NDA submission for seralutinib in PAH, and reacquired worldwide rights from Chiesi. The company also approved a convertible note exchange and reverse stock split, with cash totaling about $57 million as of June 30, 2026.PharmafileMHRA approves first lower-carbon beclometasone inhalers for asthmaThe MHRA approved the world's first pressurised metered dose inhalers using a lower-carbon propellant for asthma maintenance. The reformulated Clenil Modulite inhalers, containing beclometasone dipropionate, will be available in the UK later this year. The regulator said the new inhalers perform comparably to existing products.PR Newswire APACNSG Bio Accelerates Breakthrough Biotech Innovation in SingaporeNSG Bio has launched the NSG Bio Tomorrow initiative in partnership with Chiesi Group to support early-stage biotech startups developing solutions for respiratory and neonatal care. The initiative, called The Impulse, will provide one selected startup with one year of NSG Bio membership and dedicated laboratory access at NSG Bio Singapore. Applications open on 22 July 2026, with finalists presenting at a virtual pitch event before the selected startup is announced.The Pharma LetterMHRA approves Chiesi's carbon minimal inhaler - a world firstThe UK Medicines and Healthcare products Regulatory Agency (MHRA) approved Chiesi's Clenil Modulite inhaler formulated with next-generation propellant HFA-152a, which is non-PFAS and has low global warming potential. This authorization marks the world's first approval of pressurised metered dose inhalers using this propellant technology. The propellant delivers the inhaled dose but is not itself an active medicine.Mirage NewsMHRA OKs World's First Low-Carbon Asthma InhalersThe MHRA has approved new versions of Clenil Modulite 100 and 200 microgram inhalers using next-generation propellant HFA-152a, marking the world's first authorisation of pressurised metered-dose inhalers with this technology. The approval was granted on 21 July 2026 to Chiesi Limited, and the new low-carbon inhalers will be available in the UK later in 2026. The propellant is designed to reduce environmental impact while maintaining the same active ingredient (beclometasone dipropionate), recommended doses, and therapeutic indications as the current versions.