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SERB Pharmaceuticals

Full company profile

uuid0005v2a

Namestring
SERB Pharmaceuticals
Legal namestring
SERB S.à.r.l.
Websiteurl
serb.com
Company typeenum
Private
Founded yearint
1951
Descriptiontext

SERB Pharmaceuticals is a global specialty pharmaceutical company headquartered in Luxembourg with origins dating to 1951 in Paris (as Société d'Études et de Recherches Biologiques). Following Charterhouse Capital Partners' acquisition of a majority stake in September 2017, with co-sponsorship from Partners Group and Merieux Equity Partners, the company executed a series of transformative acquisitions — Veriton Pharma (2020), BTG Specialty Pharmaceuticals (2021), Xermelo ex-US/Japan rights from Ipsen (2022), Vistogard and Xuriden from Wellstat (2023), RSDL from Emergent BioSolutions (2024), Aurlumyn from CiVi Biopharma (2024), and Y-mAbs Therapeutics (2025) — building a portfolio of 70+ medicines focused on three franchises: rare diseases (oncology, neurology, metabolic), emergency and critical care, and CBRN medical countermeasures. The company operates a hybrid manufacturing model anchored by a proprietary polyclonal antibody manufacturing platform (one of the few globally capable of commercial-scale production with 20+ years of process know-how and two FDA-approved products) combined with in-house facilities in Wales, Australia, Utah, and Mississippi, supplemented by European contract manufacturers.

SERB generates revenue primarily through direct sales of its specialty pharmaceutical products to hospitals, healthcare systems, first responders, and emergency preparedness agencies in 18 countries across the US, Europe, and the Middle East, with a distribution partner network extending reach to 80–100+ countries. Secondary revenue mechanics include licensing and acquisition-integration economics (e.g., the €115M Idefirix licensing deal with Hansa Biopharma), government and military procurement for CBRN products such as RSDL and potassium iodide, specialty pharmacy channels in the US (BioMatrix, Cardinal Health), and direct-to-consumer e-commerce for ThyroSafe. GTM motion combines enterprise field sales, regulatory and KOL engagement, patient association partnerships, and 24/7 medical information services. The company is structured under SERB S.à.r.l. (Luxembourg) as the parent holding entity, with operating subsidiaries including BTG International (US), Protherics UK Ltd, Veriton Pharma, Y-mAbs Therapeutics, and SERB GmbH / SERB SAS / SERB Sp. z.o.o. / SERB S.A. as regional market entities across Europe.

Short descriptiontext

SERB Pharmaceuticals is a global specialty pharmaceutical company supplying 70+ medicines for rare diseases, emergency care, and CBRN medical countermeasures to healthcare providers, governments, and first responders across 100+ countries through direct sales in 18 markets and a distribution partner network.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
501–1,000
akta.pro rankint
HeadquartersLuxembourg, Luxembourg
HQ citystring
Luxembourg
HQ countrystring
Luxembourg
HQ regionstring
Europe
Markets served

Serves global market

Offices13 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
specialty pharmaceuticals, emergency care medicines, rare disease treatments, medical countermeasures, antidote manufacturing
Industry5 codes
1Specialty Care Pharmaceuticals
CodeHLAIAAABPrimaryYes
2Neurology & CNS Specialty Pharmaceuticals
CodeHLAIACACPrimaryNo
3Endocrinology & Reproductive Health Pharmaceuticals (incl. Women’s Health)
CodeHLAIAAAJPrimaryNo
4Gastroenterology & Hepatology Pharmaceuticals
CodeHLAIAAAIPrimaryNo
5Immunology & Autoimmune Specialty Pharmaceuticals
CodeHLAIACABPrimaryNo
NAICS code3 codes
  • Pharmaceutical Preparation Manufacturing325412
  • Pharmaceutical and Medicine Manufacturing3254
  • Biological Product (except Diagnostic) Manufacturing325414
SIC code2 codes
  • Pharmaceutical Preparations2834
  • Biological Products, (No Disgnostic Substances)2836
Product category
Specialty Pharmaceuticals
GTM motion3 records

Each record includes

Type, Description, Source

Revenue model3 records
1Specialty Pharmaceutical Product Sales
TypeOne Time License
Description

SERB generates revenue through the sale of its portfolio of 70+ specialty pharmaceutical products covering rare diseases, rare emergency medicine, and medical countermeasures. Products are sold through direct sales teams in the US, Europe, and Middle East, and through distribution partners in 80+ countries worldwide.

serb.com
2Licensing and Acquisition Integration
TypeLicensing Royalties
Description

SERB grows through acquiring or licensing products (e.g., Idefirix licensing from Hansa Biopharma for €115M, Y-mAbs acquisition for ~$412M) and commercialising them through its integrated platform, generating revenue from product sales in new geographies.

prnewswire.com
3Medical Countermeasure Supply
TypeHardware Sales
Description

Supply of antidotes and medical countermeasures (CBRN) to hospitals, healthcare systems, first responders, emergency preparedness agencies, and non-profit organisations, often through government procurement contracts.

serb.com
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels6 records

Each record includes

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

Cost components6 values
Personnel, Operations, Supply Chain, Marketing or Sales, Technology or R&D, Infrastructure
Pricing details1 tier
1Epistatus 10mg pre-filled syringe NHS pricing
ModelOne time/ perpetual licenseBilling cadencePay-as-you-go
Notes

NHS price: £45.76 per single 10mg in 1mL pre-filled syringe. Distributed exclusively via Alliance Healthcare for community pharmacists; hospitals order directly from Veriton Pharma.

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

SERB Pharmaceuticals is a global specialty pharmaceutical company that develops, manufactures, and commercialises a portfolio of 70+ medicines focused on emergency care, rare diseases, and medical countermeasures (including CBRN preparedness). The company acquires, licenses, or in-licenses niche products from larger pharmaceutical companies and integrates them into its commercial platform, selling directly in 18 countries (US, Europe, Middle East) and through distribution partners in 80+ additional countries. Core product categories include antidotes, antivenoms, opioid overdose reversal agents, thyroid blocking agents, rare oncology, rare neurology, and rare metabolic disease therapies.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 5 values shown
  • 90% one-year graft failure-free survival rate in highly sensitised kidney transplant patients treated with Idefirix (imlifidase) in post-authorisation study of 51 patients across 22 centres in 11 EU and UK countries
+4 more records
Product overview1 text field

SERB Pharmaceuticals is a global specialty pharmaceutical company offering a diversified portfolio of over 70 essential medicines across critical care, rare diseases, and medical countermeasures. The company operates as a platform of specialized products rather than a unified software product. The portfolio includes antidotes (Voraxaze®, DigiFab®, CroFab®, Cyanokit®, Fomepizole), emergency medicines (Aurlumyn™, RSDL®, Narcan®, ThyroSafe®), rare disease treatments (Danyelza®, Xermelo®, Vistogard®, Xuriden®, Firdapse®), and neurological therapies (Epistatus®, Mysoline®, Xenazine®). The company serves healthcare providers in over 100 countries through direct sales in 18 countries, leveraging a fully integrated pharmaceutical platform covering acquisition, development, manufacturing, launch, and commercialization of specialist medicines.

Product and service25 records
1Voraxaze (glucarpidase)
CategoryAntidote - Methotrexate Toxicity
Description

Glucarpidase 1000 units/vial powder for solution for injection; an antidote for rescue therapy in high-dose methotrexate toxicity, reducing toxic plasma methotrexate concentrations in patients with delayed elimination. Indicated for adults and children with delayed methotrexate elimination or at risk of methotrexate toxicity.

2Danyelza (naxitamab-gqgk)
CategoryRare Oncology - Neuroblastoma
Description

Naxitamab-gqgk 40mg/10ml for oncology treatment, indicated in combination with GM-CSF for relapsed or refractory high-risk neuroblastoma in bone or bone marrow. Acquired through the Y-mAbs Therapeutics acquisition.

3Cyanokit (hydroxocobalamin)
CategoryAntidote - Cyanide Poisoning
Description

Hydroxocobalamin 5g powder for solution for infusion; an antidote for cyanide poisoning treatment.

4DigiFab (digoxin immune Fab)
CategoryAntidote - Digitalis Intoxication
Description

Digoxin immune Fab (ovine) 40 mg/vial lyophilized powder for solution for intravenous injection; antidote for life-threatening digitalis intoxication. First received European regulatory approval (Swissmedic) in 2010.

5CroFab (Crotalidae Polyvalent Immune Fab)
CategoryAntivenom
Description

Crotalidae Polyvalent Immune Fab (Ovine) 1gr/vial lyophilized powder for solution for intravenous injection; antivenom for pit viper envenomation.

6Aurlumyn (iloprost IV)
CategorySevere Frostbite Treatment
Description

Iloprost injection for intravenous use; a vasodilator and platelet aggregation inhibitor, the only FDA-approved treatment for severe frostbite to reduce the risk of digit amputations.

7RSDL (Reactive Skin Decontamination Lotion)
CategoryMedical Countermeasure - CBRN
Description

Medical device with DAM and KBDO pre-impregnated foam sponge applicator pad for skin decontamination; FDA-cleared device to remove or neutralize chemical warfare agents from the skin in one step.

8Vistogard (uridine triacetate)
CategoryAntidote - Chemotherapy Overdose
Description

Uridine triacetate 10g oral granules; emergency treatment for adult and pediatric patients following fluorouracil or capecitabine overdose.

9Xuriden (uridine triacetate)
CategoryRare Metabolic Disorder Treatment
Description

Uridine triacetate 2g; treatment for hereditary orotic aciduria (HOA) in adult and pediatric patients.

10Xermelo (telotristat ethyl)
CategoryRare Oncology - Carcinoid Syndrome
Description

Telotristat ethyl 250 mg; treatment for carcinoid syndrome diarrhoea in combination with somatostatin analogue therapy in adults inadequately controlled by SSA therapy.

11ThyroSafe (Potassium Iodide Tablets)
CategoryMedical Countermeasure - Radiation
Description

Potassium iodide tablets USP 130mg; thyroid blocking medicine for use in nuclear radiation emergencies to protect the thyroid gland from radioactive iodine uptake. Also available as Kaliumjodid SERB 65mg in Germany.

12Epistatus (midazolam oromucosal solution)
CategoryRare Neurological - Epilepsy
Description

Midazolam 2.5mg, 5mg, 7.5mg or 10mg oromucosal solution pre-filled syringe; anticonvulsant for treatment of prolonged acute convulsive seizures in children and adolescents aged 10 to less than 18 years.

13Firdapse (amifampridine)
CategoryRare Neurological Treatment
Description

Amifampridine 10mg; treatment for rare neurological conditions (Lambert-Eaton myasthenic syndrome). Licensed from BioMarin for Europe in 2019.

14Radiogardase (Prussian blue)
CategoryAntidote - Radioactive Contamination
Description

Prussian blue 500mg capsules; antidote for internal contamination with radioactive cesium and thallium. Licensed from Heyl Pharmaceuticals in 2013.

15Fomepizole SERB
CategoryAntidote - Toxic Alcohol Poisoning
Description

Fomepizole 5mg/ml concentrate for solution for infusion; antidote for ethylene glycol and methanol poisoning.

16Narcan (naloxone)
CategoryAntidote - Opioid Overdose
Description

Naloxone 0.4mg/ml; antidote and opioid antagonist for emergency reversal of opioid overdose.

17Gamma-OH (hydroxy-4 butyric acid)
CategoryGeneral Anaesthetic
Description

Hydroxy-4 butyric acid 200mg/ml solution for injection (IV); general anesthetic agent.

18Xenazine (tetrabenazine)
CategoryRare Neurological - Movement Disorders
Description

Tetrabenazine 25mg scored tablets; treatment for movement disorders including chorea associated with Huntington's disease.

19Mysoline (primidone)
CategoryRare Neurological - Antiepileptic
Description

Primidone 50mg or 250mg; antiepileptic for seizure management.

20Collatamp G
CategorySurgical Haemostatic Implant
Description

Collagen 2.8 mg/cm2 with gentamicin sulfate 2.0 mg/cm2 implant; collagen haemostatic agent with antimicrobial properties for surgical use.

21Custodiol (HTK solution)
CategoryOrgan Preservation Medical Device
Description

Solution HTK for organ and tissue procurement; medical device for organ preservation during transplant procedures.

22Toxogonin (obidoxime chloride)
CategoryAntidote - Organophosphate Poisoning
Description

Obidoxime chloride 250mg; cholinesterase reactivator for organophosphate poisoning treatment. Acquired from Merck in 2017.

23B.A.L. (dimercaprol)
CategoryAntidote - Heavy Metal Chelation
Description

Dimercaprol 200mg with Butacaine 1mg solution for I.M. injection; heavy metal chelator for arsenic, mercury, and gold poisoning.

24L-Thyroxine SERB
CategoryThyroid Hormone Therapy
Description

Levothyroxine sodium 200µg/ml solution for injection/infusion; thyroid hormone replacement therapy.

25Idefirix (imlifidase)
CategoryRare Disease - Transplant Desensitisation
Description

Imlifidase; a treatment for desensitisation of highly sensitised adult patients prior to kidney transplantation from deceased donors. Conditionally approved in EU, Norway, Liechtenstein, Iceland, and UK.

Scale indicator10 records

Each record includes

Type, Value, Description, Source

Partnership11 partners
Strategic tierCoreTypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2026-05-19
Description

Exclusive licensing agreement granting SERB development and commercialisation rights to Idefirix (imlifidase) for highly sensitised kidney transplant patients across EU, UK, Switzerland, Norway, Liechtenstein, Iceland, and MENA. Hansa receives €110M upfront plus €5M upon EMA filing acceptance. SERB assumes responsibility for PAES follow-up and paediatric study upon becoming MAH.

Strategic tierMinorTypeImplementation/ SI/ Consulting PartnerAnnounced on2026-05-19
Description

Rothschild & Co. acted as exclusive financial advisor and Freshfields as legal counsel to SERB for the Idefirix licensing agreement. Centerview Partners UK LLP and Morgan Lewis served equivalent roles for Hansa Biopharma.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-09-16
Description

SERB completed acquisition of Y-mAbs Therapeutics, a commercial-stage biopharma focused on antibody-based cancer therapeutics, for approximately $412M (all-cash, $8.60/share, ~105% premium). Y-mAbs became a wholly owned subsidiary of SERB and was delisted from Nasdaq. Key asset Danyelza (naxitamab-gqgk) strengthens SERB's rare oncology portfolio.

Strategic tierMinorTypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2024-10-21
Description

SERB acquired Aurlumyn (iloprost IV), the only FDA-approved treatment for severe frostbite in the US, from CiVi Biopharma. Aurlumyn received priority review and orphan drug designation, approved February 2024. SERB planned to make it available for the winter season following acquisition.

Strategic tierMinorTypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2024-07-31
Description

SERB acquired RSDL (Reactive Skin Decontamination Lotion) kit for approximately $75M upfront plus $5M milestone, including the leased manufacturing facility in Hattiesburg, Mississippi. RSDL is the only FDA-cleared device to remove/neutralise chemical warfare agents from skin, with 20 years of clinical data and 15M+ packets sold in 30+ countries.

Strategic tierMinorTypeImplementation/ SI/ Consulting PartnerAnnounced on2024-07-31
Description

Rothschild & Co acted as exclusive financial advisor and Freshfields as legal counsel to SERB for the RSDL acquisition.

Strategic tierMinorTypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2023-07-13
Description

SERB acquired Vistogard (uridine triacetate) for 5-FU/capecitabine overdose and Xuriden (uridine triacetate) for hereditary orotic aciduria from Wellstat Therapeutics. Products are commercially available in the US and distributed in Europe on named patient/compassionate use basis. SERB's BTG Pharmaceuticals entity sells products in the US.

Strategic tierMinorTypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2022-04-04
Description

SERB acquired rights from Ipsen to commercialise Xermelo (telotristat ethyl) for carcinoid syndrome diarrhoea outside the US and Japan. Countries with market authorisation include Europe, Switzerland, Great Britain, Canada, Israel, Australia, Saudi Arabia, Mexico, and Russia.

9EMA/CHMP (European Regulatory)
Strategic tierMinorTypeOthersAnnounced on2022-01-14
Description

European Medicines Agency Committee for Human Medicinal Products issued positive opinion leading to EU marketing authorisation for Voraxaze (glucarpidase) for high-dose methotrexate toxicity. Approved in all EU member states plus Iceland, Liechtenstein, and Norway.

serb.com
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2021-03-01
Description

SERB acquired BTG Specialty Pharmaceuticals (division of Boston Scientific) for an undisclosed amount, creating a global leader in critical care medicines. BTG brought US commercial presence, bio-manufacturing facilities in Wales, Australia, and Utah, and products including CroFab, Voraxaze, and DigiFab. The combined company had around 400 employees in 11 offices with direct presence across all major pharmaceutical markets.

Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2020-05-20
Description

SERB acquired Veriton Pharma, a private pharmaceutical company specialising in licensed and unlicensed medicines for patients with special requirements, headquartered in Weybridge, UK with offices in Middle East and Australia. Portfolio of 60+ specialised formulations supplying 25+ countries. Added direct commercial presence in UK, Middle East, and Australia.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight7 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Rare disease specialist within AstraZeneca, focused on complement-mediated and rare neurological/oncology indications. Comparable rare-disease positioning and US/EU commercial footprint.

TypeBroad incumbent
Description

Global specialty pharmaceutical company with branded and generic injectables, including hospital specialty products. Comparable in supplying critical-care injectables (antidotes, anaesthesia, hospital specialty) across multiple geographies.

TypeDirect peer
Description

European specialty pharmaceutical company focused on rare diseases across immunology, haematology, and specialty care. Comparable in business model — rare-disease franchise, European heritage, strong specialty commercial platform.

TypeBroad incumbent
Description

European specialty pharma in oncology, rare disease, and neuroscience. Previously owned Xermelo (now licensed to SERB); comparable product portfolio focus on specialty/rare indications and European commercial model.

TypeBroad incumbent
Description

Global specialty pharma focused on neuroscience and oncology, with several orphan/rare disease assets. Comparable commercial focus on specialty care, orphan drugs, and acquisition-driven growth.

TypeEmerging player
Description

Specialty pharma focused on non-opioid pain management and hospital-based therapeutics. Comparable in focusing on hospital-administered specialty products with limited competition and strong pricing power, though in different therapeutic categories.

TypeDirect peer
Description

Swedish biopharma developing imlifidase (Idefirix) for kidney transplantation and rare immunology indications. Direct transaction counterparty to SERB (May 2026, €115M licensing deal) and a direct comparator in the transplant desensitisation space.

TypeBroad incumbent
Description

Specialty pharma focused on iron deficiency, nephrology, and rare diseases. Comparable European specialty/rare disease commercial platform and overlap in transplant/nephrology patient segments with SERB's Idefirix.

TypeDirect peer
Description

US-based specialty pharma focused on CBRN medical countermeasures and antidotes. Directly comparable to SERB as the prior owner of RSDL (acquired by SERB in 2024) and a leading supplier to government stockpiling programs.

TypeBroad incumbent
Description

European specialty pharma with a dedicated rare disease business (Orphan Europe) and broad specialty care portfolio. Comparable mix of rare disease and specialty care products with European and US commercial presence.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses6 records

Each record includes

Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks7 records

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Headline, Details, Source

Key highlights7 records

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Headline, Details, Source

Customer concentration

Classification, Details

Named customers5 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
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature2 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles13 records

Each record includes

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

Subsidiaries12 records

Each record includes

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

Compliance1 record

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&A1 record

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 →

SERB Pharmaceuticals

Specialty Pharmaceuticalsserb.com

SERB Pharmaceuticals is a global specialty pharmaceutical company supplying 70+ medicines for rare diseases, emergency care, and CBRN medical countermeasures to healthcare providers, governments, and first responders across 100+ countries through direct sales in 18 markets and a distribution partner network.

What SERB Pharmaceuticals does

SERB Pharmaceuticals is a global specialty pharmaceutical company headquartered in Luxembourg with origins dating to 1951 in Paris (as Société d'Études et de Recherches Biologiques). Following Charterhouse Capital Partners' acquisition of a majority stake in September 2017, with co-sponsorship from Partners Group and Merieux Equity Partners, the company executed a series of transformative acquisitions — Veriton Pharma (2020), BTG Specialty Pharmaceuticals (2021), Xermelo ex-US/Japan rights from Ipsen (2022), Vistogard and Xuriden from Wellstat (2023), RSDL from Emergent BioSolutions (2024), Aurlumyn from CiVi Biopharma (2024), and Y-mAbs Therapeutics (2025) — building a portfolio of 70+ medicines focused on three franchises: rare diseases (oncology, neurology, metabolic), emergency and critical care, and CBRN medical countermeasures. The company operates a hybrid manufacturing model anchored by a proprietary polyclonal antibody manufacturing platform (one of the few globally capable of commercial-scale production with 20+ years of process know-how and two FDA-approved products) combined with in-house facilities in Wales, Australia, Utah, and Mississippi, supplemented by European contract manufacturers.

SERB generates revenue primarily through direct sales of its specialty pharmaceutical products to hospitals, healthcare systems, first responders, and emergency preparedness agencies in 18 countries across the US, Europe, and the Middle East, with a distribution partner network extending reach to 80–100+ countries. Secondary revenue mechanics include licensing and acquisition-integration economics (e.g., the €115M Idefirix licensing deal with Hansa Biopharma), government and military procurement for CBRN products such as RSDL and potassium iodide, specialty pharmacy channels in the US (BioMatrix, Cardinal Health), and direct-to-consumer e-commerce for ThyroSafe. GTM motion combines enterprise field sales, regulatory and KOL engagement, patient association partnerships, and 24/7 medical information services. The company is structured under SERB S.à.r.l. (Luxembourg) as the parent holding entity, with operating subsidiaries including BTG International (US), Protherics UK Ltd, Veriton Pharma, Y-mAbs Therapeutics, and SERB GmbH / SERB SAS / SERB Sp. z.o.o. / SERB S.A. as regional market entities across Europe.

SERB Pharmaceuticals firmographics

Firmographics
Name
SERB Pharmaceuticals
Legal name
SERB S.à.r.l.
Website
https://serb.com
Company type
Private
Founded year
1951
Operating status
Operating
Headcount range
501–1,000 employees
Short description
SERB Pharmaceuticals is a global specialty pharmaceutical company supplying 70+ medicines for rare diseases, emergency care, and CBRN medical countermeasures to healthcare providers, governments, and first responders across 100+ countries through direct sales in 18 markets and a distribution partner network.
Ownership category
akta.pro rank

SERB Pharmaceuticals industry classification

Industry
Product category
Specialty Pharmaceuticals
NAICS
Pharmaceutical Preparation Manufacturing (325412), 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
Specialty Care Pharmaceuticals (HLAIAAAB)
akta.pro secondary industries
Neurology & CNS Specialty Pharmaceuticals (HLAIACAC), Endocrinology & Reproductive Health Pharmaceuticals (incl. Women’s Health) (HLAIAAAJ), Gastroenterology & Hepatology Pharmaceuticals (HLAIAAAI), Immunology & Autoimmune Specialty Pharmaceuticals (HLAIACAB)

Keywords

  • Specialty pharmaceuticals
  • Emergency care medicines
  • Rare disease treatments
  • Medical countermeasures
  • Antidote manufacturing

Where SERB Pharmaceuticals is headquartered

Location

Headquarters

HQ city
Luxembourg
HQ country
Luxembourg
HQ region
Europe

Offices13 records

Markets served

SERB Pharmaceuticals business model

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

Revenue model

  1. Specialty Pharmaceutical Product Sales: SERB generates revenue through the sale of its portfolio of 70+ specialty pharmaceutical products covering rare diseases, rare emergency medicine, and medical countermeasures. Products are sold through direct sales teams in the US, Europe, and Middle East, and through distribution partners in 80+ countries worldwide.
  2. Licensing and Acquisition Integration: SERB grows through acquiring or licensing products (e.g., Idefirix licensing from Hansa Biopharma for €115M, Y-mAbs acquisition for ~$412M) and commercialising them through its integrated platform, generating revenue from product sales in new geographies.
  3. Medical Countermeasure Supply: Supply of antidotes and medical countermeasures (CBRN) to hospitals, healthcare systems, first responders, emergency preparedness agencies, and non-profit organisations, often through government procurement contracts.

Pricing tiers

ModelBillingPrice
One time/ perpetual licensePay-as-you-goEpistatus 10mg pre-filled syringe NHS pricing

Go-to-market motion3 records

Distribution channels6 records

Marketing channels6 records

SERB Pharmaceuticals product offering

Product offering

Core offering

SERB Pharmaceuticals is a global specialty pharmaceutical company that develops, manufactures, and commercialises a portfolio of 70+ medicines focused on emergency care, rare diseases, and medical countermeasures (including CBRN preparedness). The company acquires, licenses, or in-licenses niche products from larger pharmaceutical companies and integrates them into its commercial platform, selling directly in 18 countries (US, Europe, Middle East) and through distribution partners in 80+ additional countries. Core product categories include antidotes, antivenoms, opioid overdose reversal agents, thyroid blocking agents, rare oncology, rare neurology, and rare metabolic disease therapies.

Product overview

SERB Pharmaceuticals is a global specialty pharmaceutical company offering a diversified portfolio of over 70 essential medicines across critical care, rare diseases, and medical countermeasures. The company operates as a platform of specialized products rather than a unified software product. The portfolio includes antidotes (Voraxaze®, DigiFab®, CroFab®, Cyanokit®, Fomepizole), emergency medicines (Aurlumyn™, RSDL®, Narcan®, ThyroSafe®), rare disease treatments (Danyelza®, Xermelo®, Vistogard®, Xuriden®, Firdapse®), and neurological therapies (Epistatus®, Mysoline®, Xenazine®). The company serves healthcare providers in over 100 countries through direct sales in 18 countries, leveraging a fully integrated pharmaceutical platform covering acquisition, development, manufacturing, launch, and commercialization of specialist medicines.

Differentiator

Problem solved

Functional benefit

Products and services

  • Voraxaze (glucarpidase) Glucarpidase 1000 units/vial powder for solution for injection; an antidote for rescue therapy in high-dose methotrexate toxicity, reducing toxic plasma methotrexate concentrations in patients with delayed elimination. Indicated for adults and children with delayed methotrexate elimination or at risk of methotrexate toxicity.
  • Danyelza (naxitamab-gqgk) Naxitamab-gqgk 40mg/10ml for oncology treatment, indicated in combination with GM-CSF for relapsed or refractory high-risk neuroblastoma in bone or bone marrow. Acquired through the Y-mAbs Therapeutics acquisition.
  • Cyanokit (hydroxocobalamin) Hydroxocobalamin 5g powder for solution for infusion; an antidote for cyanide poisoning treatment.
  • DigiFab (digoxin immune Fab) Digoxin immune Fab (ovine) 40 mg/vial lyophilized powder for solution for intravenous injection; antidote for life-threatening digitalis intoxication. First received European regulatory approval (Swissmedic) in 2010.
  • CroFab (Crotalidae Polyvalent Immune Fab) Crotalidae Polyvalent Immune Fab (Ovine) 1gr/vial lyophilized powder for solution for intravenous injection; antivenom for pit viper envenomation.
  • Aurlumyn (iloprost IV) Iloprost injection for intravenous use; a vasodilator and platelet aggregation inhibitor, the only FDA-approved treatment for severe frostbite to reduce the risk of digit amputations.
  • RSDL (Reactive Skin Decontamination Lotion) Medical device with DAM and KBDO pre-impregnated foam sponge applicator pad for skin decontamination; FDA-cleared device to remove or neutralize chemical warfare agents from the skin in one step.
  • Vistogard (uridine triacetate) Uridine triacetate 10g oral granules; emergency treatment for adult and pediatric patients following fluorouracil or capecitabine overdose.
  • Xuriden (uridine triacetate) Uridine triacetate 2g; treatment for hereditary orotic aciduria (HOA) in adult and pediatric patients.
  • Xermelo (telotristat ethyl) Telotristat ethyl 250 mg; treatment for carcinoid syndrome diarrhoea in combination with somatostatin analogue therapy in adults inadequately controlled by SSA therapy.
  • ThyroSafe (Potassium Iodide Tablets) Potassium iodide tablets USP 130mg; thyroid blocking medicine for use in nuclear radiation emergencies to protect the thyroid gland from radioactive iodine uptake. Also available as Kaliumjodid SERB 65mg in Germany.
  • Epistatus (midazolam oromucosal solution) Midazolam 2.5mg, 5mg, 7.5mg or 10mg oromucosal solution pre-filled syringe; anticonvulsant for treatment of prolonged acute convulsive seizures in children and adolescents aged 10 to less than 18 years.
  • Firdapse (amifampridine) Amifampridine 10mg; treatment for rare neurological conditions (Lambert-Eaton myasthenic syndrome). Licensed from BioMarin for Europe in 2019.
  • Radiogardase (Prussian blue) Prussian blue 500mg capsules; antidote for internal contamination with radioactive cesium and thallium. Licensed from Heyl Pharmaceuticals in 2013.
  • Fomepizole SERB Fomepizole 5mg/ml concentrate for solution for infusion; antidote for ethylene glycol and methanol poisoning.
  • Narcan (naloxone) Naloxone 0.4mg/ml; antidote and opioid antagonist for emergency reversal of opioid overdose.
  • Gamma-OH (hydroxy-4 butyric acid) Hydroxy-4 butyric acid 200mg/ml solution for injection (IV); general anesthetic agent.
  • Xenazine (tetrabenazine) Tetrabenazine 25mg scored tablets; treatment for movement disorders including chorea associated with Huntington's disease.
  • Mysoline (primidone) Primidone 50mg or 250mg; antiepileptic for seizure management.
  • Collatamp G Collagen 2.8 mg/cm2 with gentamicin sulfate 2.0 mg/cm2 implant; collagen haemostatic agent with antimicrobial properties for surgical use.
  • Custodiol (HTK solution) Solution HTK for organ and tissue procurement; medical device for organ preservation during transplant procedures.
  • Toxogonin (obidoxime chloride) Obidoxime chloride 250mg; cholinesterase reactivator for organophosphate poisoning treatment. Acquired from Merck in 2017.
  • B.A.L. (dimercaprol) Dimercaprol 200mg with Butacaine 1mg solution for I.M. injection; heavy metal chelator for arsenic, mercury, and gold poisoning.
  • L-Thyroxine SERB Levothyroxine sodium 200µg/ml solution for injection/infusion; thyroid hormone replacement therapy.
  • Idefirix (imlifidase) Imlifidase; a treatment for desensitisation of highly sensitised adult patients prior to kidney transplantation from deceased donors. Conditionally approved in EU, Norway, Liechtenstein, Iceland, and UK.

Quantifiable outcome

  • 90% one-year graft failure-free survival rate in highly sensitised kidney transplant patients treated with Idefirix (imlifidase) in post-authorisation study of 51 patients across 22 centres in 11 EU and UK countries
  • +4 more outcomes

Companies that use SERB Pharmaceuticals

Customer profile

Named customers5 records

Segments3 records

Ideal customer profiles4 records

SERB Pharmaceuticals technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature2 records

SERB Pharmaceuticals partnerships and signals

Strategic signal

Partnerships

Eleven partnerships are on record, tiered core and minor.

  • Hansa Biopharma ABcoreOEM/ Whitelabel/ Licensing Partner · 19 May 2026Exclusive licensing agreement granting SERB development and commercialisation rights to Idefirix (imlifidase) for highly sensitised kidney transplant patients across EU, UK, Switzerland, Norway, Liechtenstein, Iceland, and MENA. Hansa receives €110M upfront plus €5M upon EMA filing acceptance. SERB assumes responsibility for PAES follow-up and paediatric study upon becoming MAH.
  • Rothschild & Co. (financial advisor) and Freshfields (legal counsel)minorImplementation/ SI/ Consulting Partner · 19 May 2026Rothschild & Co. acted as exclusive financial advisor and Freshfields as legal counsel to SERB for the Idefirix licensing agreement. Centerview Partners UK LLP and Morgan Lewis served equivalent roles for Hansa Biopharma.
  • Y-mAbs TherapeuticscoreStrategic or Co-development Partner · 16 September 2025SERB completed acquisition of Y-mAbs Therapeutics, a commercial-stage biopharma focused on antibody-based cancer therapeutics, for approximately $412M (all-cash, $8.60/share, ~105% premium). Y-mAbs became a wholly owned subsidiary of SERB and was delisted from Nasdaq. Key asset Danyelza (naxitamab-gqgk) strengthens SERB's rare oncology portfolio.
  • CiVi BiopharmaminorOEM/ Whitelabel/ Licensing Partner · 21 October 2024SERB acquired Aurlumyn (iloprost IV), the only FDA-approved treatment for severe frostbite in the US, from CiVi Biopharma. Aurlumyn received priority review and orphan drug designation, approved February 2024. SERB planned to make it available for the winter season following acquisition.
  • Emergent BioSolutions Inc.minorOEM/ Whitelabel/ Licensing Partner · 31 July 2024SERB acquired RSDL (Reactive Skin Decontamination Lotion) kit for approximately $75M upfront plus $5M milestone, including the leased manufacturing facility in Hattiesburg, Mississippi. RSDL is the only FDA-cleared device to remove/neutralise chemical warfare agents from skin, with 20 years of clinical data and 15M+ packets sold in 30+ countries.
  • Rothschild & Co. (financial advisor) and Freshfields (legal counsel)minorImplementation/ SI/ Consulting Partner · 31 July 2024Rothschild & Co acted as exclusive financial advisor and Freshfields as legal counsel to SERB for the RSDL acquisition.
  • Wellstat TherapeuticsminorOEM/ Whitelabel/ Licensing Partner · 13 July 2023SERB acquired Vistogard (uridine triacetate) for 5-FU/capecitabine overdose and Xuriden (uridine triacetate) for hereditary orotic aciduria from Wellstat Therapeutics. Products are commercially available in the US and distributed in Europe on named patient/compassionate use basis. SERB's BTG Pharmaceuticals entity sells products in the US.
  • IpsenminorOEM/ Whitelabel/ Licensing Partner · 4 April 2022SERB acquired rights from Ipsen to commercialise Xermelo (telotristat ethyl) for carcinoid syndrome diarrhoea outside the US and Japan. Countries with market authorisation include Europe, Switzerland, Great Britain, Canada, Israel, Australia, Saudi Arabia, Mexico, and Russia.
  • EMA/CHMP (European Regulatory)minorOthers · 14 January 2022European Medicines Agency Committee for Human Medicinal Products issued positive opinion leading to EU marketing authorisation for Voraxaze (glucarpidase) for high-dose methotrexate toxicity. Approved in all EU member states plus Iceland, Liechtenstein, and Norway.
  • BTG Specialty Pharmaceuticals (acquired from Boston Scientific)coreStrategic or Co-development Partner · 1 March 2021SERB acquired BTG Specialty Pharmaceuticals (division of Boston Scientific) for an undisclosed amount, creating a global leader in critical care medicines. BTG brought US commercial presence, bio-manufacturing facilities in Wales, Australia, and Utah, and products including CroFab, Voraxaze, and DigiFab. The combined company had around 400 employees in 11 offices with direct presence across all major pharmaceutical markets.
  • Veriton PharmaminorStrategic or Co-development Partner · 20 May 2020SERB acquired Veriton Pharma, a private pharmaceutical company specialising in licensed and unlicensed medicines for patients with special requirements, headquartered in Weybridge, UK with offices in Middle East and Australia. Portfolio of 60+ specialised formulations supplying 25+ countries. Added direct commercial presence in UK, Middle East, and Australia.

Scale indicators10 records

Recent moves6 records

Expansion highlights7 records

SERB Pharmaceuticals competitors and assessment

Company assessment

Broad incumbents

  • Alexion (AstraZeneca Rare Disease): Rare disease specialist within AstraZeneca, focused on complement-mediated and rare neurological/oncology indications. Comparable rare-disease positioning and US/EU commercial footprint.
  • Hikma Pharmaceuticals: Global specialty pharmaceutical company with branded and generic injectables, including hospital specialty products. Comparable in supplying critical-care injectables (antidotes, anaesthesia, hospital specialty) across multiple geographies.
  • Ipsen: European specialty pharma in oncology, rare disease, and neuroscience. Previously owned Xermelo (now licensed to SERB); comparable product portfolio focus on specialty/rare indications and European commercial model.
  • Jazz Pharmaceuticals: Global specialty pharma focused on neuroscience and oncology, with several orphan/rare disease assets. Comparable commercial focus on specialty care, orphan drugs, and acquisition-driven growth.
  • Vifor Pharma (CSL Vifor): Specialty pharma focused on iron deficiency, nephrology, and rare diseases. Comparable European specialty/rare disease commercial platform and overlap in transplant/nephrology patient segments with SERB's Idefirix.
  • Recordati: European specialty pharma with a dedicated rare disease business (Orphan Europe) and broad specialty care portfolio. Comparable mix of rare disease and specialty care products with European and US commercial presence.

Direct peers

  • Swedish Orphan Biovitrum (Sobi): European specialty pharmaceutical company focused on rare diseases across immunology, haematology, and specialty care. Comparable in business model — rare-disease franchise, European heritage, strong specialty commercial platform.
  • Hansa Biopharma: Swedish biopharma developing imlifidase (Idefirix) for kidney transplantation and rare immunology indications. Direct transaction counterparty to SERB (May 2026, €115M licensing deal) and a direct comparator in the transplant desensitisation space.
  • Emergent BioSolutions: US-based specialty pharma focused on CBRN medical countermeasures and antidotes. Directly comparable to SERB as the prior owner of RSDL (acquired by SERB in 2024) and a leading supplier to government stockpiling programs.

Emerging players

  • Pacira BioSciences: Specialty pharma focused on non-opioid pain management and hospital-based therapeutics. Comparable in focusing on hospital-administered specialty products with limited competition and strong pricing power, though in different therapeutic categories.

Market position

Strengths5 records

Weaknesses6 records

Competitive moat5 records

Key risks7 records

Key highlights7 records

Customer concentration

SERB Pharmaceuticals social profiles

Digital presence

SERB Pharmaceuticals compliance and trust

Trust signal

Compliance1 record

SERB Pharmaceuticals financial estimates

Financial estimate

Revenue estimate

Valuation estimate

SERB Pharmaceuticals leadership team

Management profile

Number of profiles

Profiles13 records

SERB Pharmaceuticals subsidiaries and ownership

Company hierarchy

Subsidiaries12 records

SERB Pharmaceuticals funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

SERB Pharmaceuticals M&A and investment

M&A and investment

M&A1 record

Investments

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

Frequently asked questions about SERB Pharmaceuticals

What does SERB Pharmaceuticals do?

SERB Pharmaceuticals is a global specialty pharmaceutical company that develops, manufactures, and commercialises a portfolio of 70+ medicines focused on emergency care, rare diseases, and medical countermeasures (including CBRN preparedness). The company acquires, licenses, or in-licenses niche products from larger pharmaceutical companies and integrates them into its commercial platform, selling directly in 18 countries (US, Europe, Middle East) and through distribution partners in 80+ additional countries. Core product categories include antidotes, antivenoms, opioid overdose reversal agents, thyroid blocking agents, rare oncology, rare neurology, and rare metabolic disease therapies.

Is SERB Pharmaceuticals a public or private company?

SERB Pharmaceuticals is a private company. It is classified as private equity controlled and is currently operating.

When was SERB Pharmaceuticals founded?

SERB Pharmaceuticals was founded in 1951. It employs 501 to 1,000 people.

Where is SERB Pharmaceuticals based?

SERB Pharmaceuticals is headquartered in Luxembourg, Luxembourg, in the Europe region.

How does SERB Pharmaceuticals make money?

Three revenue lines are on record. Specialty Pharmaceutical Product Sales are the primary driver. The others are licensing and Acquisition Integration and medical Countermeasure Supply.

Who are SERB Pharmaceuticals's main competitors?

Broad incumbents on record are Alexion (AstraZeneca Rare Disease), Hikma Pharmaceuticals, Ipsen, Jazz Pharmaceuticals, Vifor Pharma (CSL Vifor) and Recordati. Direct peers are Swedish Orphan Biovitrum (Sobi), Hansa Biopharma and Emergent BioSolutions. Pacira BioSciences is listed as an emerging player.

Does SERB Pharmaceuticals have an API?

No public API is recorded for SERB Pharmaceuticals.

What industry is SERB Pharmaceuticals in?

SERB Pharmaceuticals's product category is Specialty Pharmaceuticals. Its primary akta.pro industry code is HLAIAAAB, Specialty Care Pharmaceuticals, with a secondary code of HLAIACAC, Neurology & CNS Specialty Pharmaceuticals. Its NAICS code is 325412 and its SIC code is 2834.

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Live signals
PR NewswireOsteosarcoma Market is Set to Rise by 2036 as 8 Emerging Therapies Set to Drive Future Growth | DelveInsightDelveInsight forecasts the osteosarcoma market to grow from about $60 million in 2025 to a higher value by 2036, driven by eight emerging therapies. The market is projected to expand at a 9% CAGR through 2036, with OST-HER2 expected to generate $37 million by 2036.European BiotechnologyHansa takes first step toward US Nasdaq listingHansa plans to seek a Nasdaq Global Market listing under ticker HNSA, while retaining its Stockholm listing. The company is considering a concurrent European private placement. The FDA is reviewing imlifidase after positive Phase 3 data, with a decision due Dec. 19.HCP LiveREVERSE-IT: Bentracimab Effective in Reversing Ticagrelor Antiplatelet EffectsData from the REVERSE-IT trial presented at the ACC 2025 Annual Scientific Sessions demonstrate that bentracimab effectively and rapidly reverses the antiplatelet effects of ticagrelor, restoring normal clotting within minutes. The drug was developed by SFJ Pharmaceuticals and is set for US commercialization by SERB Pharmaceuticals, with an application currently under FDA review. This development addresses a critical clinical need for managing life-threatening bleeding or facilitating urgent surgery in patients taking ticagrelor.PharmExecTreating Poisonings: The Demand for Antidotes in PharmaSERB Pharmaceuticals is focusing on the increasing demand for antidotes to treat poisonings and toxicities, particularly in light of global events such as the COVID pandemic and conflicts in Ukraine. The company has doubled its manufacturing capability to address the surge in need for potassium iodide products and is also developing new antidotes for various toxins and pathogens, highlighting a growing urgency for public health preparedness. SERB aims to enhance its rapid response capabilities through innovative antidote development.BioSpaceOpinion: Why moving from Big Pharma to specialty changes everythingThomas Kolaras, a professional who transitioned from working in large pharmaceutical companies to SERB Pharmaceuticals, argues that moving to a midsize specialty pharma company creates new opportunities for sharpened thinking and leadership. The author contends that specialty pharma offers greater accountability and proximity to patients compared to the process-driven, function-specific environment of large organizations. Kolaras suggests that the transition is not about abandoning strategic work but rather about gaining end-to-end ownership and faster professional growth through direct engagement with the full patient and stakeholder journey.PR NewswireHansa Biopharma announces closing of €115 million licensing transaction with SERB Pharmaceuticals for Idefirix in Europe and MENAHansa Biopharma and SERB Pharmaceuticals have closed a €115 million exclusive licensing transaction for Idefirix, a first-in-class treatment for highly sensitized kidney transplant patients, covering the EU, UK, Switzerland, Norway, Liechtenstein, Iceland, and MENA region. The deal comprises an €110 million upfront payment and a €5 million milestone upon EMA filing acceptance for full approval. The transaction strengthens Hansa's financial position as it prepares for a potential US launch of imlifidase, subject to FDA approval by the PDUFA date of December 19, 2026.European BiotechnologyHansa data supports full approval plan for IdefirixHansa reported that Idefirix met its primary objective in a confirmatory study, with 90% of patients achieving one-year graft failure-free survival. The data support a full marketing authorisation application by end of 2026, and Hansa agreed to hand European commercial rights to SERB for €110m upfront.Pharmaceutical TechnologySERB signs agreement to acquire Idefirix rights for $133.6mSERB Pharmaceuticals has signed an agreement to acquire exclusive development and commercialisation rights to the drug Idefirix from Hansa Biopharma for €115m ($133.6m). The deal covers the European Union, Iceland, Liechtenstein, Norway, Switzerland, the UK, and the MENA region, with SERB assuming responsibility for long-term follow-up studies after the EMA review process. Completion is expected within 60 days pending customary regulatory clearances.PR NewswireHansa Biopharma enters into €115 million licensing agreement with SERB Pharmaceuticals for IDEFIRIX in Europe and MENAHansa Biopharma AB and SERB S.A. announced an exclusive licensing agreement for IDEFIRIX (imlifidase), granting SERB rights to develop and commercialize the treatment for highly sensitized kidney transplant patients across the EU, UK, Switzerland, Norway, Liechtenstein, Iceland, and MENA regions. Hansa will receive €110 million upfront plus €5 million upon EMA filing acceptance for full approval, with the transaction expected to close within 60 days pending FDI regulatory approval. The agreement is described by Hansa's CEO as transformative, strengthening the company's financial position and providing a pathway to profitability tied to a 2026 U.S. FDA approval decision.GlobeNewswireSERB Pharmaceuticals to acquire European and MENA rights to Idefirix® (imlifidase) from Hansa Biopharma for €115 millionSERB Pharmaceuticals has entered into an agreement to acquire exclusive development and commercialization rights to Idefirix® (imlifidase) from Hansa Biopharma AB for €115 million, covering the European Union, United Kingdom, Switzerland, Norway, Liechtenstein, Iceland, and the MENA region. Idefirix® is a treatment for desensitizing highly sensitized adult patients prior to kidney transplantation from deceased donors, addressing a condition affecting approximately 10–15% of the 70,000 Europeans with end-stage renal disease awaiting transplants each year. Hansa will receive €110 million upfront and an additional €5 million upon EMA acceptance of a filing for full approval, with the transaction subject to FDI regulatory approval expected within 60 days.