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Immedica

Full company profile

uuid0004scb

Namestring
Immedica
Legal namestring
Immedica Pharma AB
Websiteurl
immedica.com
Company typeenum
Private
Founded yearint
2018
Descriptiontext

Immedica Pharma AB is a Stockholm-headquartered, privately held pharmaceutical company founded in 2018 that commercializes medicines for rare diseases and specialty care across more than 50 countries via wholly-owned subsidiaries in Europe, the Middle East and North Africa, and, since September 2024, a U.S. commercial hub in Chicago. The company is jointly owned by KKR-managed investment funds and Nordic healthcare investor Impilo AB following a September 2024 acquisition financed in part by a €320 million Hayfin-co-led single-asset continuation fund, and is led by CEO Anders Edvell with a senior team drawn heavily from Sobi/Swedish Orphan Biovitrum and other large-pharma rare-disease organizations.

The commercial portfolio is organized into four core therapeutic areas (RARE Metabolic, RARE Hematology & Oncology, RARE Neurology, RARE Endocrinology) plus Specialty Care and is assembled through a mix of proprietary biologics, in-licensing and acquisitions rather than in-house drug discovery. Flagship proprietary/lead assets include Loargys (pegzilarginase), the first and only disease-modifying treatment for Arginase 1 Deficiency with FDA accelerated approval in February 2026 and EU marketing authorization since December 2023; Ztalmy (ganaxolone), the first FDA-approved treatment for seizures associated with CDKL5 deficiency disorder, acquired via the $151 million Marinus Pharmaceuticals takeover in January 2025; Zepzelca (lurbinectedin) for small cell lung cancer; and Efmody and Alkindi (modified-release and oral-granule hydrocortisone) for adrenal insufficiency and congenital adrenal hyperplasia, acquired via the $65 million Neurocrine/Diurnal deal in January 2026. Supporting products include Ravicti, Ammonaps and Orphacol for urea cycle disorders, Neofordex, Akynzeo, Aloxi and Yondelis, alongside a CE-marked in vitro diagnostic (Nor-NOHA Blood Collection Tubes) that anchors ARG1-D diagnosis.

Immedica generates revenue primarily through direct commercialization of proprietary and in-licensed pharmaceutical products, supplemented by royalty streams (notably a $7 million ganaxolone royalty buy-back from Ovid Therapeutics in June 2025) and exclusive distribution agreements with regional partners such as PharmaMar (Zepzelca), OrphanPacific (Ravicti in Japan), Innovative Medicines Group (Loargys in Latin America) and WinHealth (China). Pricing is not publicly disclosed and is negotiated country-by-country with national reimbursement authorities (G-BA in Germany, NICE in the UK, MENA regulators), with U.S. distribution for Loargys routed through specialty pharmacy partner Orsini. Since 2018, Immedica has executed 16 strategic transactions, scaled from 7 to more than 140 employees, and reported FY2023 net sales of SEK 905 million (~USD 85 million) at a 66% gross margin, with annual revenue growth cited above 50% at the time of the 2024 KKR acquisition.

Short descriptiontext

Immedica is a Stockholm-based, KKR/Impilo-owned pharmaceutical company that commercializes proprietary, in-licensed and acquired medicines for rare diseases and specialty care across 50+ countries in Europe, MENA, the U.S. and Asia.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
101–250
akta.pro rankint
HeadquartersStockholm, Sweden
HQ citystring
Stockholm
HQ countrystring
Sweden
HQ regionstring
Europe
Markets served

Serves global market

Offices13 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
rare disease pharmaceuticals, specialty care commercialization, orphan drug distribution, in-licensed biologics, metabolic disorder therapeutics
Industry3 codes
1Specialty Injectable & Infusion Therapies (Cross-therapeutic)
CodeHLAIACAOPrimaryYes
2Specialty Care Pharmaceuticals
CodeHLAIAAABPrimaryNo
3Immunoglobulins & Passive Immunization Biologics (IVIG, hyperimmune globulins, antitoxins)
CodeHLAAAEAHPrimaryNo
NAICS code4 codes
  • Pharmaceutical Preparation Manufacturing325412
  • Medicinal and Botanical Manufacturing325411
  • Medical and Diagnostic Laboratories62151
  • Biological Product (except Diagnostic) Manufacturing325414
SIC code3 codes
  • Wholesale-Drugs, Proprietaries & Druggists' Sundries5122
  • Pharmaceutical Preparations2834
  • Surgical & Medical Instruments & Apparatus3841
Product category
Specialty Pharmaceuticals (Rare Disease)
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model3 records
1Pharmaceutical Product Sales (Commercialization)
TypeHardware Sales
Description

Immedica generates revenue through the commercialization and direct sales of proprietary and in-licensed rare disease and specialty care pharmaceutical products across more than 50 countries, including Loargys, Ztalmy, Efmody, Alkindi, Ravicti, Zepzelca, Ammonaps, Orphacol, Akynzeo, Aloxi, Neofordex and Yondelis.

immedica.com
2Royalty Acquisitions / Royalty Income
TypeLicensing Royalties
Description

Immedica purchased future ganaxolone royalty rights from Ovid Therapeutics for $7M, allowing it to capture royalty streams on Ztalmy revenues.

ainvest.com
3In-licensing & Distribution Agreements
TypeLicensing Royalties
Description

Immedica earns revenue through in-licensing and exclusive distribution deals where it commercializes third-party products in its geographies (e.g., Zepzelca partnership with PharmaMar, Ravicti in Japan with OrphanPacific, Loargys in Latin America with Innovative Medicines Group).

immedica.com
Distribution channels4 records

Each record includes

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

Cost components6 values
Personnel, Supply Chain, Operations, Marketing or Sales, Technology or R&D, Infrastructure
Pricing details1 tier
1Not publicly disclosed; quote-based / reimbursement negotiated by country
ModelOtherBilling cadencePay-as-you-go
Notes

Pricing for Immedica's orphan and rare disease products is not publicly listed on the company website. Pricing and reimbursement are negotiated per country through local authorities and payers (e.g., G-BA assessments in Germany, NICE backing in UK, MENA registration authorities). Distribution in some markets occurs via specialty pharmacy (Orsini in the U.S. for LOARGYS) and named patient use (NPU).

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

Immedica commercializes proprietary, in-licensed, and acquired pharmaceutical products for rare diseases and specialty care across more than 50 countries in Europe, MENA, and the U.S. Its portfolio spans four therapeutic areas (RARE Metabolic, RARE Hematology & Oncology, RARE Neurology, RARE Endocrinology) plus Specialty Care, marketed under brands such as Loargys, Ztalmy, Efmody, Alkindi, Zepzelca, Ravicti, Ammonaps, Orphacol, Yondelis, Akynzeo, Aloxi, and Neofordex. It also supplies the Nor-NOHA Blood Collection Tubes in vitro diagnostic device supporting Arginase 1 Deficiency diagnosis.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

Immedica is a Stockholm-headquartered pharmaceutical company focused on the commercialization of medicines for rare diseases and specialty care, supplying patients in more than 50 countries via its own commercial platforms in Europe, MENA, and the U.S. The portfolio is organized around four core therapeutic areas (RARE Metabolic, RARE Hematology & Oncology, RARE Neurology, RARE Endocrinology) plus Specialty Care, and is built through a mix of proprietary, in-licensed, and acquired products rather than a single integrated software platform. Proprietary/lead rare disease assets include Loargys® (pegzilarginase) for Arginase 1 Deficiency, Ztalmy® (ganaxolone) for CDKL5 deficiency disorder, Efmody® (modified-release hydrocortisone) and Alkindi® for adrenal insufficiency/CAH, and Zepzelca® (lurbinectedin) for small cell lung cancer. Supporting/in-licensed products include Ravicti®, Ammonaps®, Orphacol®, Neofordex®, Akynzeo®, Aloxi®, and Yondelis®, complemented by the Nor-NOHA Blood Collection Tubes in vitro diagnostic device and a Specialty Care ophthalmology portfolio. Together these products form a multi-asset rare disease and specialty care franchise rather than a unified single-product offering.

Product and service13 records
1Loargys (pegzilarginase)
CategoryRare metabolic pharmaceutical product (proprietary)
2Ztalmy (ganaxolone)
CategoryRare neurology pharmaceutical product (acquired proprietary)
3Efmody (modified-release hydrocortisone)
CategoryRare endocrinology pharmaceutical product (acquired proprietary)
4Alkindi (hydrocortisone oral granules)
CategoryRare endocrinology pharmaceutical product (acquired proprietary)
5Zepzelca (lurbinectedin)
CategoryRare hematology & oncology pharmaceutical product (in-licensed)
6Ravicti (glycerol phenylbutyrate)
CategoryRare metabolic pharmaceutical product (in-licensed)
7Ammonaps (sodium phenylbutyrate)
CategoryRare metabolic pharmaceutical product (in-licensed)
8Orphacol (cholic acid)
CategoryRare metabolic pharmaceutical product (in-licensed)
9Yondelis (trabectedin)
CategoryRare hematology & oncology pharmaceutical product (in-licensed)
10Akynzeo (netupitant and palonosetron)
CategorySpecialty care pharmaceutical product (in-licensed)
11Aloxi (palonosetron)
CategorySpecialty care pharmaceutical product (in-licensed)
12Neofordex (high-dose dexamethasone)
CategorySpecialty care pharmaceutical product (in-licensed)
13Nor-NOHA Blood Collection Tubes
CategoryIn vitro diagnostic medical device
Scale indicator9 records

Each record includes

Type, Value, Description, Source

Partnership8 partners
Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2026-03-27
Description

Immedica has a partnership with PharmaMar for distribution of Zepzelca (lurbinectedin) in various regions. Immedica holds distribution rights for Zepzelca in the Middle East and North Africa (MENA) and other regions. Zepzelca + atezolizumab received positive CHMP opinion as first-line maintenance therapy for extensive-stage small cell lung cancer.

Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2026-03-09
Description

Orsini was selected by Immedica Pharma US Inc. as the exclusive specialty pharmacy and hub services partner for LOARGYS (pegzilarginase-nbln), a treatment for hyperargininemia caused by Arginase 1 Deficiency, in the U.S. The partnership involves providing specialty pharmacy, hub, and logistics services to facilitate patient access, including ultra-cold storage at the Columbus, Ohio facility.

Strategic tierFlagshipTypeStrategic or Co-development PartnerAnnounced on2026-01-21
Description

Immedica completed the acquisition of Neurocrine Group Limited and its subsidiaries from Neurocrine Biosciences for USD 65 million in cash on January 21, 2026. The deal includes global rights to Alkindi (hydrocortisone oral granules) and global rights ex-US to Efmody (hydrocortisone modified-release capsules), establishing rare endocrinology as a new therapeutic area for Immedica.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-12-22
Description

Immedica and OrphanPacific jointly announced approval of Ravicti (glycerol phenylbutyrate) in Japan for the treatment of urea cycle disorders (UCDs). OrphanPacific serves as Immedica's partner for the Japanese market entry.

Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2025-10-01
Description

Immedica and Innovative Medicines Group entered an agreement on Loargys (pegzilarginase) in Latin America. The agreement expands Immedica's reach for Loargys into Latin American markets through IMG's regional distribution capabilities.

Strategic tierFlagshipTypeStrategic or Co-development PartnerAnnounced on2025-01-06
Description

Immedica acquired Marinus Pharmaceuticals in a $151 million cash tender offer deal at $0.55 per share. The acquisition brings Ztalmy (ganaxolone), the first FDA-approved treatment for seizures associated with CDKL5 deficiency disorder, into Immedica's portfolio, significantly expanding its US market presence with a revenue-generating commercial product.

Strategic tierCoreTypeChannel Partner/ Reseller/ Distributor
Description

Immedica has access to the Chinese market through partnership with the Chinese company WinHealth Pharma. Through this partnership, Immedica helps patients with UCD (Urea Cycle Disorder) in China and surrounding regions.

8Various US and European biotech partners
Strategic tierCoreTypeStrategic or Co-development Partner
Description

Immedica has a broad partnering model with US biotech and European companies, executing 16 acquisitions and licensing/distribution agreements since 2018. Their business model is built on partnerships, and they continuously evaluate new business opportunities. They conduct annual partner satisfaction surveys and focus on partnering excellence.

immedica.com
Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Ireland-headquartered specialty pharmaceutical company focused on rare neurological conditions (epilepsy, narcolepsy) and oncology, with commercial operations across the U.S. and Europe; comparable as a high-growth rare disease specialty pharma with similar in-licensing and acquisition-driven model.

TypeBroad incumbent
Description

Ireland-headquartered rare disease specialty pharma (now owned by Amgen) with a focus on rare inflammatory, autoimmune and endocrine diseases (Tepezza, Krystexxa, Ravicti until divestiture); Immedica's Dan Camardo is a former Horizon executive, indicating direct operational and strategic overlap.

TypeDirect peer
Description

U.S.-based rare disease-focused biotech commercializing enzyme replacement therapies for ultra-rare metabolic disorders (phenylketonuria, MPS, CLN2); highly comparable to Immedica's RARE Metabolic franchise and Loargys positioning, though at significantly larger scale.

TypeDirect peer
Description

Global biotechnology company with a focused rare disease franchise in cystic fibrosis and a growing pipeline in sickle cell disease, beta-thalassemia and pain; comparable as a high-margin specialty pharma with disease-modifying rare disease assets commanding premium pricing.

TypeDirect peer
Description

Italian specialty pharmaceutical group with a dedicated Recordati Rare Diseases unit commercializing treatments for rare metabolic, endocrine and neurological conditions globally; comparable business model focused on in-licensing and commercializing rare disease assets in Europe and beyond.

TypeBroad incumbent
Description

Acquired by AstraZeneca in 2021, Alexion is a global leader in rare disease specialty pharma (paroxysmal nocturnal hemoglobinuria, hypophosphatasia, neuromyelitis optica) with deep U.S. commercial infrastructure; a broader incumbent against which Immedica competes in the rare hematology/metabolic space.

TypeEmerging player
Description

U.S.-based clinical-stage and commercial rare disease biotech focused on metabolic diseases, with approved therapies for X-linked hypophosphatemia and other ultrarare conditions; emerging player in the same niche as Immedica's RARE Metabolic franchise (e.g., ARG1-D, urea cycle disorders).

TypeDirect peer
Description

Swedish-headquartered rare disease specialty pharmaceutical company focused on hematology, immunology and specialty care, with global commercial infrastructure across Europe, MENA and North America; the most direct comparable to Immedica given shared Swedish heritage, rare disease focus, and similar therapeutic area mix.

TypeBroad incumbent
Description

Pre-acquisition Shire was a global leader in rare disease specialty pharma with franchises in hematology, immunology, GI and neurology; now part of Takeda's Rare Diseases business unit, it represents a broad incumbent whose model of acquiring and commercializing rare disease assets across geographies mirrors Immedica's strategy.

TypeDirect peer
Description

European-focused rare disease subsidiary of Recordati commercializing treatments for metabolic, endocrine and neurological rare diseases across EU and MENA; most operationally comparable to Immedica's European commercial model and target indication mix.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers1 record

Each record includes

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

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 maturity
App detail

Has app

Feature5 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles14 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

Compliance3 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds1 record

Each record includes

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

Investors1 record

Each record includes

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

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

M&A2 records

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment1 record

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 →

Immedica

Specialty Pharmaceuticals (Rare Disease)immedica.com

Immedica is a Stockholm-based, KKR/Impilo-owned pharmaceutical company that commercializes proprietary, in-licensed and acquired medicines for rare diseases and specialty care across 50+ countries in Europe, MENA, the U.S. and Asia.

What Immedica does

Immedica Pharma AB is a Stockholm-headquartered, privately held pharmaceutical company founded in 2018 that commercializes medicines for rare diseases and specialty care across more than 50 countries via wholly-owned subsidiaries in Europe, the Middle East and North Africa, and, since September 2024, a U.S. commercial hub in Chicago. The company is jointly owned by KKR-managed investment funds and Nordic healthcare investor Impilo AB following a September 2024 acquisition financed in part by a €320 million Hayfin-co-led single-asset continuation fund, and is led by CEO Anders Edvell with a senior team drawn heavily from Sobi/Swedish Orphan Biovitrum and other large-pharma rare-disease organizations.

The commercial portfolio is organized into four core therapeutic areas (RARE Metabolic, RARE Hematology & Oncology, RARE Neurology, RARE Endocrinology) plus Specialty Care and is assembled through a mix of proprietary biologics, in-licensing and acquisitions rather than in-house drug discovery. Flagship proprietary/lead assets include Loargys (pegzilarginase), the first and only disease-modifying treatment for Arginase 1 Deficiency with FDA accelerated approval in February 2026 and EU marketing authorization since December 2023; Ztalmy (ganaxolone), the first FDA-approved treatment for seizures associated with CDKL5 deficiency disorder, acquired via the $151 million Marinus Pharmaceuticals takeover in January 2025; Zepzelca (lurbinectedin) for small cell lung cancer; and Efmody and Alkindi (modified-release and oral-granule hydrocortisone) for adrenal insufficiency and congenital adrenal hyperplasia, acquired via the $65 million Neurocrine/Diurnal deal in January 2026. Supporting products include Ravicti, Ammonaps and Orphacol for urea cycle disorders, Neofordex, Akynzeo, Aloxi and Yondelis, alongside a CE-marked in vitro diagnostic (Nor-NOHA Blood Collection Tubes) that anchors ARG1-D diagnosis.

Immedica generates revenue primarily through direct commercialization of proprietary and in-licensed pharmaceutical products, supplemented by royalty streams (notably a $7 million ganaxolone royalty buy-back from Ovid Therapeutics in June 2025) and exclusive distribution agreements with regional partners such as PharmaMar (Zepzelca), OrphanPacific (Ravicti in Japan), Innovative Medicines Group (Loargys in Latin America) and WinHealth (China). Pricing is not publicly disclosed and is negotiated country-by-country with national reimbursement authorities (G-BA in Germany, NICE in the UK, MENA regulators), with U.S. distribution for Loargys routed through specialty pharmacy partner Orsini. Since 2018, Immedica has executed 16 strategic transactions, scaled from 7 to more than 140 employees, and reported FY2023 net sales of SEK 905 million (~USD 85 million) at a 66% gross margin, with annual revenue growth cited above 50% at the time of the 2024 KKR acquisition.

Immedica firmographics

Firmographics
Name
Immedica
Legal name
Immedica Pharma AB
Website
https://immedica.com
Company type
Private
Founded year
2018
Operating status
Operating
Headcount range
101–250 employees
Short description
Immedica is a Stockholm-based, KKR/Impilo-owned pharmaceutical company that commercializes proprietary, in-licensed and acquired medicines for rare diseases and specialty care across 50+ countries in Europe, MENA, the U.S. and Asia.
Ownership category
akta.pro rank

Immedica industry classification

Industry
Product category
Specialty Pharmaceuticals (Rare Disease)
NAICS
Pharmaceutical Preparation Manufacturing (325412), Medicinal and Botanical Manufacturing (325411), Medical and Diagnostic Laboratories (62151), Biological Product (except Diagnostic) Manufacturing (325414)
SIC
Wholesale-Drugs, Proprietaries & Druggists' Sundries (5122), Pharmaceutical Preparations (2834), Surgical & Medical Instruments & Apparatus (3841)
akta.pro primary industry
Specialty Injectable & Infusion Therapies (Cross-therapeutic) (HLAIACAO)
akta.pro secondary industries
Specialty Care Pharmaceuticals (HLAIAAAB), Immunoglobulins & Passive Immunization Biologics (IVIG, hyperimmune globulins, antitoxins) (HLAAAEAH)

Keywords

  • Rare disease pharmaceuticals
  • Specialty care commercialization
  • Orphan drug distribution
  • In-licensed biologics
  • Metabolic disorder therapeutics

Where Immedica is headquartered

Location

Headquarters

HQ city
Stockholm
HQ country
Sweden
HQ region
Europe

Offices13 records

Markets served

Immedica business model

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

Revenue model

  1. Pharmaceutical Product Sales (Commercialization): Immedica generates revenue through the commercialization and direct sales of proprietary and in-licensed rare disease and specialty care pharmaceutical products across more than 50 countries, including Loargys, Ztalmy, Efmody, Alkindi, Ravicti, Zepzelca, Ammonaps, Orphacol, Akynzeo, Aloxi, Neofordex and Yondelis.
  2. Royalty Acquisitions / Royalty Income: Immedica purchased future ganaxolone royalty rights from Ovid Therapeutics for $7M, allowing it to capture royalty streams on Ztalmy revenues.
  3. In-licensing & Distribution Agreements: Immedica earns revenue through in-licensing and exclusive distribution deals where it commercializes third-party products in its geographies (e.g., Zepzelca partnership with PharmaMar, Ravicti in Japan with OrphanPacific, Loargys in Latin America with Innovative Medicines Group).

Pricing tiers

ModelBillingPrice
OtherPay-as-you-goNot publicly disclosed; quote-based / reimbursement negotiated by country

Go-to-market motion1 record

Distribution channels4 records

Immedica product offering

Product offering

Core offering

Immedica commercializes proprietary, in-licensed, and acquired pharmaceutical products for rare diseases and specialty care across more than 50 countries in Europe, MENA, and the U.S. Its portfolio spans four therapeutic areas (RARE Metabolic, RARE Hematology & Oncology, RARE Neurology, RARE Endocrinology) plus Specialty Care, marketed under brands such as Loargys, Ztalmy, Efmody, Alkindi, Zepzelca, Ravicti, Ammonaps, Orphacol, Yondelis, Akynzeo, Aloxi, and Neofordex. It also supplies the Nor-NOHA Blood Collection Tubes in vitro diagnostic device supporting Arginase 1 Deficiency diagnosis.

Product overview

Immedica is a Stockholm-headquartered pharmaceutical company focused on the commercialization of medicines for rare diseases and specialty care, supplying patients in more than 50 countries via its own commercial platforms in Europe, MENA, and the U.S. The portfolio is organized around four core therapeutic areas (RARE Metabolic, RARE Hematology & Oncology, RARE Neurology, RARE Endocrinology) plus Specialty Care, and is built through a mix of proprietary, in-licensed, and acquired products rather than a single integrated software platform. Proprietary/lead rare disease assets include Loargys® (pegzilarginase) for Arginase 1 Deficiency, Ztalmy® (ganaxolone) for CDKL5 deficiency disorder, Efmody® (modified-release hydrocortisone) and Alkindi® for adrenal insufficiency/CAH, and Zepzelca® (lurbinectedin) for small cell lung cancer. Supporting/in-licensed products include Ravicti®, Ammonaps®, Orphacol®, Neofordex®, Akynzeo®, Aloxi®, and Yondelis®, complemented by the Nor-NOHA Blood Collection Tubes in vitro diagnostic device and a Specialty Care ophthalmology portfolio. Together these products form a multi-asset rare disease and specialty care franchise rather than a unified single-product offering.

Differentiator

Problem solved

Functional benefit

Products and services

  • Loargys (pegzilarginase)
  • Ztalmy (ganaxolone)
  • Efmody (modified-release hydrocortisone)
  • Alkindi (hydrocortisone oral granules)
  • Zepzelca (lurbinectedin)
  • Ravicti (glycerol phenylbutyrate)
  • Ammonaps (sodium phenylbutyrate)
  • Orphacol (cholic acid)
  • Yondelis (trabectedin)
  • Akynzeo (netupitant and palonosetron)
  • Aloxi (palonosetron)
  • Neofordex (high-dose dexamethasone)
  • Nor-NOHA Blood Collection Tubes

Companies that use Immedica

Customer profile

Named customers1 record

Ideal customer profiles3 records

Immedica technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature5 records

Immedica partnerships and signals

Strategic signal

Partnerships

Eight partnerships are on record, tiered core and flagship.

  • PharmaMarcoreChannel Partner/ Reseller/ Distributor · 27 March 2026Immedica has a partnership with PharmaMar for distribution of Zepzelca (lurbinectedin) in various regions. Immedica holds distribution rights for Zepzelca in the Middle East and North Africa (MENA) and other regions. Zepzelca + atezolizumab received positive CHMP opinion as first-line maintenance therapy for extensive-stage small cell lung cancer.
  • OrsinicoreChannel Partner/ Reseller/ Distributor · 9 March 2026Orsini was selected by Immedica Pharma US Inc. as the exclusive specialty pharmacy and hub services partner for LOARGYS (pegzilarginase-nbln), a treatment for hyperargininemia caused by Arginase 1 Deficiency, in the U.S. The partnership involves providing specialty pharmacy, hub, and logistics services to facilitate patient access, including ultra-cold storage at the Columbus, Ohio facility.
  • Neurocrine Biosciences (Diurnal Group acquisition)flagshipStrategic or Co-development Partner · 21 January 2026Immedica completed the acquisition of Neurocrine Group Limited and its subsidiaries from Neurocrine Biosciences for USD 65 million in cash on January 21, 2026. The deal includes global rights to Alkindi (hydrocortisone oral granules) and global rights ex-US to Efmody (hydrocortisone modified-release capsules), establishing rare endocrinology as a new therapeutic area for Immedica.
  • OrphanPacificcoreStrategic or Co-development Partner · 22 December 2025Immedica and OrphanPacific jointly announced approval of Ravicti (glycerol phenylbutyrate) in Japan for the treatment of urea cycle disorders (UCDs). OrphanPacific serves as Immedica's partner for the Japanese market entry.
  • Innovative Medicines GroupcoreChannel Partner/ Reseller/ Distributor · 1 October 2025Immedica and Innovative Medicines Group entered an agreement on Loargys (pegzilarginase) in Latin America. The agreement expands Immedica's reach for Loargys into Latin American markets through IMG's regional distribution capabilities.
  • Marinus PharmaceuticalsflagshipStrategic or Co-development Partner · 6 January 2025Immedica acquired Marinus Pharmaceuticals in a $151 million cash tender offer deal at $0.55 per share. The acquisition brings Ztalmy (ganaxolone), the first FDA-approved treatment for seizures associated with CDKL5 deficiency disorder, into Immedica's portfolio, significantly expanding its US market presence with a revenue-generating commercial product.
  • WinHealth PharmacoreChannel Partner/ Reseller/ DistributorImmedica has access to the Chinese market through partnership with the Chinese company WinHealth Pharma. Through this partnership, Immedica helps patients with UCD (Urea Cycle Disorder) in China and surrounding regions.
  • Various US and European biotech partnerscoreStrategic or Co-development PartnerImmedica has a broad partnering model with US biotech and European companies, executing 16 acquisitions and licensing/distribution agreements since 2018. Their business model is built on partnerships, and they continuously evaluate new business opportunities. They conduct annual partner satisfaction surveys and focus on partnering excellence.

Scale indicators9 records

Recent moves7 records

Expansion highlights6 records

Immedica competitors and assessment

Company assessment

Direct peers

  • Jazz Pharmaceuticals: Ireland-headquartered specialty pharmaceutical company focused on rare neurological conditions (epilepsy, narcolepsy) and oncology, with commercial operations across the U.S. and Europe; comparable as a high-growth rare disease specialty pharma with similar in-licensing and acquisition-driven model.
  • BioMarin Pharmaceutical: U.S.-based rare disease-focused biotech commercializing enzyme replacement therapies for ultra-rare metabolic disorders (phenylketonuria, MPS, CLN2); highly comparable to Immedica's RARE Metabolic franchise and Loargys positioning, though at significantly larger scale.
  • Vertex Pharmaceuticals: Global biotechnology company with a focused rare disease franchise in cystic fibrosis and a growing pipeline in sickle cell disease, beta-thalassemia and pain; comparable as a high-margin specialty pharma with disease-modifying rare disease assets commanding premium pricing.
  • Recordati Rare Diseases: Italian specialty pharmaceutical group with a dedicated Recordati Rare Diseases unit commercializing treatments for rare metabolic, endocrine and neurological conditions globally; comparable business model focused on in-licensing and commercializing rare disease assets in Europe and beyond.
  • Swedish Orphan Biovitrum (Sobi): Swedish-headquartered rare disease specialty pharmaceutical company focused on hematology, immunology and specialty care, with global commercial infrastructure across Europe, MENA and North America; the most direct comparable to Immedica given shared Swedish heritage, rare disease focus, and similar therapeutic area mix.
  • Orphan Europe (Recordati subsidiary): European-focused rare disease subsidiary of Recordati commercializing treatments for metabolic, endocrine and neurological rare diseases across EU and MENA; most operationally comparable to Immedica's European commercial model and target indication mix.

Broad incumbents

  • Horizon Therapeutics (Amgen): Ireland-headquartered rare disease specialty pharma (now owned by Amgen) with a focus on rare inflammatory, autoimmune and endocrine diseases (Tepezza, Krystexxa, Ravicti until divestiture); Immedica's Dan Camardo is a former Horizon executive, indicating direct operational and strategic overlap.
  • Alexion (AstraZeneca Rare Disease): Acquired by AstraZeneca in 2021, Alexion is a global leader in rare disease specialty pharma (paroxysmal nocturnal hemoglobinuria, hypophosphatasia, neuromyelitis optica) with deep U.S. commercial infrastructure; a broader incumbent against which Immedica competes in the rare hematology/metabolic space.
  • Shire (now Takeda Rare Diseases): Pre-acquisition Shire was a global leader in rare disease specialty pharma with franchises in hematology, immunology, GI and neurology; now part of Takeda's Rare Diseases business unit, it represents a broad incumbent whose model of acquiring and commercializing rare disease assets across geographies mirrors Immedica's strategy.

Emerging players

  • Ultragenyx Pharmaceutical: U.S.-based clinical-stage and commercial rare disease biotech focused on metabolic diseases, with approved therapies for X-linked hypophosphatemia and other ultrarare conditions; emerging player in the same niche as Immedica's RARE Metabolic franchise (e.g., ARG1-D, urea cycle disorders).

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks6 records

Key highlights7 records

Customer concentration

Immedica social profiles

Digital presence

Immedica compliance and trust

Trust signal

Compliance3 records

Immedica financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Immedica leadership team

Management profile

Number of profiles

Profiles14 records

Immedica subsidiaries and ownership

Company hierarchy

Subsidiaries12 records

Immedica funding detail

Funding detail

Funding overview

Funding rounds1 record

Investors1 record

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Immedica M&A and investment

M&A and investment

M&A2 records

Investments1 record

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Frequently asked questions about Immedica

What does Immedica do?

Immedica commercializes proprietary, in-licensed, and acquired pharmaceutical products for rare diseases and specialty care across more than 50 countries in Europe, MENA, and the U.S. Its portfolio spans four therapeutic areas (RARE Metabolic, RARE Hematology & Oncology, RARE Neurology, RARE Endocrinology) plus Specialty Care, marketed under brands such as Loargys, Ztalmy, Efmody, Alkindi, Zepzelca, Ravicti, Ammonaps, Orphacol, Yondelis, Akynzeo, Aloxi, and Neofordex. It also supplies the Nor-NOHA Blood Collection Tubes in vitro diagnostic device supporting Arginase 1 Deficiency diagnosis.

Is Immedica a public or private company?

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

When was Immedica founded?

Immedica was founded in 2018. It employs 101 to 250 people.

Where is Immedica based?

Immedica is headquartered in Stockholm, Sweden, in the Europe region.

How does Immedica make money?

Three revenue lines are on record. Pharmaceutical Product Sales (Commercialization) is the primary driver. The others are royalty Acquisitions / Royalty Income and in-licensing & Distribution Agreements.

Who are Immedica's main competitors?

Direct peers on record are Jazz Pharmaceuticals, BioMarin Pharmaceutical, Vertex Pharmaceuticals, Recordati Rare Diseases, Swedish Orphan Biovitrum (Sobi) and Orphan Europe (Recordati subsidiary). Broad incumbents are Horizon Therapeutics (Amgen), Alexion (AstraZeneca Rare Disease) and Shire (now Takeda Rare Diseases). Ultragenyx Pharmaceutical is listed as an emerging player.

Does Immedica have an API?

No public API is recorded for Immedica.

What industry is Immedica in?

Immedica's product category is Specialty Pharmaceuticals (Rare Disease). Its primary akta.pro industry code is HLAIACAO, Specialty Injectable & Infusion Therapies (Cross-therapeutic), with a secondary code of HLAIAAAB, Specialty Care Pharmaceuticals. Its NAICS code is 325412 and its SIC code is 5122.

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Live signals
news.cision.comAbstract highlighting three-year ganaxolone data in CDD presented at EEC 2026Immedica Pharma presented three-year ganaxolone data for CDKL5 deficiency disorder at EEC 2026. The analysis of 88 patients showed sustained seizure reductions, with 42.1% achieving ≥50% reduction in major motor seizures after 163 weeks. No new safety findings emerged.news.cision.comZepzelca® (lurbinectedin) in combination with atezolizumab approved as first-line maintenance therapy for extensive-stage small cell lung cancer in KuwaitImmedica announced that Zepzelca (lurbinectedin) plus atezolizumab is approved as first-line maintenance for extensive-stage small cell lung cancer in Kuwait. The Phase 3 IMforte trial showed a 46% reduction in progression or death risk and 27% reduction in death risk versus atezolizumab alone. The results were presented at ASCO 2025 and published in The Lancet.news.cision.comImmedica receives Orphan Drug Designation for pegzilarginase in JapanJapan's Ministry of Health, Labor and Welfare granted Orphan Drug Designation to pegzilarginase for arginase 1 deficiency. The designation makes the drug eligible for a priority review process, and Immedica plans to submit a Japanese New Drug Application.njFDA discloses why drugs don’t make it to market. A pharma company says it’s bad for businessA pharmaceutical company has filed an anonymous petition with the FDA asking the agency to reconsider its policy of publicly disclosing Complete Response Letters, which explain why drug applications are rejected, arguing it gives competitors free access to confidential strategies. The FDA has shifted its practice since April 2025, pausing CRL publications, and has requested Congress grant formal legal authority to continue disclosures while planning a formal rule for October. Companies like Capricor Therapeutics and Immedica are cited as examples where CRL disclosures revealed specific FDA recommendations or omitted company rebuttals, raising competitive concerns.news.cision.comEfmody® (modified-release hydrocortisone) granted extension of indication for adrenal insufficiencyThe European Commission has granted Immedica Pharma an extension of indication for Efmody® (modified-release hydrocortisone) to include treatment of adrenal insufficiency in adolescents aged 12 years and over and adults. Efmody® is a modified-release formulation designed to replicate the natural circadian rhythm of cortisol using a twice-daily regimen. The approval, based on study DIUR-016-AI, marks an expansion from the drug's existing indication for congenital adrenal hyperplasia.news.cision.comImmedica announces first marketing authorization approval in the MENA region for Ztalmy® (ganaxolone) for CDKL5 deficiency disorderImmedica announced that the Kuwait Ministry of Health has granted marketing authorization for Ztalmy® (ganaxolone) for the treatment of seizures associated with CDKL5 deficiency disorder in patients two years of age and older. This approval marks the first authorization for Ztalmy in the Middle East and North Africa region. The milestone underscores Immedica's commitment to expanding access to rare disease therapies in underserved markets.news.cision.comZepzelca® (lurbinectedin) in combination with atezolizumab receives positive CHMP opinion as first-line maintenance therapy for extensive-stage small cell lung cancerImmedica Pharma AB announced that Zepzelca (lurbinectedin) in combination with atezolizumab received a positive opinion from the European Medicines Agency's CHMP as first-line maintenance therapy for adults with extensive-stage small cell lung cancer whose disease has not progressed following induction therapy. The Phase 3 IMforte trial demonstrated that this combination reduced the risk of disease progression or death by 46% and the risk of death by 27% compared to atezolizumab maintenance alone, with median overall survival of 13.2 months versus 10.6 months. The CHMP opinion will now be reviewed by the European Commission for final marketing authorization decision in the EU.PR NewswireOrsini Selected by Immedica Pharma US Inc. as Exclusive Specialty Pharmacy and Hub Services Partner for LOARGYS® (pegzilarginase-nbln)Orsini has been selected by Immedica Pharma US Inc. as the exclusive specialty pharmacy and hub services partner for LOARGYS® (pegzilarginase-nbln), the first and only FDA-approved therapy for Arginase 1 Deficiency (ARG1-D), an ultra-rare metabolic disease affecting approximately 250 people in the U.S. Under the partnership, Orsini will provide integrated specialty pharmacy services, hub services for patient access support including insurance coverage and financial assistance, and 3PL services to facilitate commercialization of the therapy. The collaboration enables Orsini to leverage its rare disease pharmacy capabilities while supporting Immedica's launch of the treatment for patients aged 2 years and older.news.cision.comRavicti® (glycerol phenylbutyrate) approved in United Arab Emirates and Sultanate of OmanImmedica Pharma AB announced regulatory approval of Ravicti® (glycerol phenylbutyrate) in the United Arab Emirates and Sultanate of Oman, expanding access to treatment for patients with urea cycle disorders in the region. The drug is now approved across five Middle Eastern markets including Saudi Arabia, Kuwait, Qatar, Oman, and the UAE. The Stockholm-based pharmaceutical company, focused on rare diseases and backed by investment firms KKR and Impilo, stated that these approvals underscore its long-term commitment to the rare disease community in the Middle East.FiercePharmaImmedica overcomes prior FDA rebuke for ultrarare disease med to score new approvalThe FDA has granted accelerated approval to Immedica Pharma's Loargys (pegzilarginase) for treating hyperargininemia in Arginase 1 deficiency (ARG1-D), a rare genetic disorder affecting approximately 250 patients in the U.S. age 2 and older. The approval comes four years after the FDA refused to file the original application from Aeglea BioTherapeutics in 2022; Aeglea subsequently sold the asset to Immedica for $15 million upfront plus $100 million in milestones. Loargys, which lowers plasma arginine through a weekly infusion, is the first treatment to directly address the enzyme deficiency rather than manage symptoms, and the drug is expected to be available in the U.S. in April.