PHARNasdaqPharmaceutical PreparationsUS GAAP · USD

Pharming Group N.V.

Pharming Group N.V. is a Dutch biopharmaceutical company focused on medicines for rare, debilitating, and life-threatening diseases. Its business combines the development and commercialization of small-molecule and biologic therapies through operations in Europe and the United States.

Revenue376m USD
+26.6 %y/y
Operating profit (EBIT)23.6m USD
+9,518.8 %y/y
EBIT margin6.3%
+6.2 ppy/y
Net income2.9m USD
+124.1 %y/y
Free cash flow54.0m USD
+2,182.3 %y/y

Fiscal year 2025 · change from previous year

Development 2022–2025

-1000100200300400m USD2022: 206 m USD2022: EBIT 20 m USD20222023: 245 m USD2023: EBIT -6.0 m USD20232024: 297 m USD2024: EBIT 0.25 m USD20242025: 376 m USD2025: EBIT 24 m USD202537624
RevenueOperating profit (EBIT)

Business

Share of revenue
Commercial rare-disease medicines90 %

Approved therapies sold to patients with rare immune and inflammatory diseases.

Biologic therapies55 %

Protein-based medicines developed and commercialized for specialty indications.

Small-molecule therapies45 %

Oral or chemically synthesized medicines used in rare-disease treatment.

Pipeline and development programs0 %

Research and clinical programs intended to expand the rare-disease portfolio.

Customers

Pharming sells into the rare-disease treatment ecosystem, where demand is driven by specialist physicians, hospitals, and treatment centers managing complex genetic or immunological disorders. Patients ultimately receive the therapies through healthcare providers and reimbursing payers, so access and diagnosis are important commercial drivers. The company also depends on healthcare systems and pharmacies that support specialty-drug distribution.

Specialist physicians and clinics

Prescribe RUCONEST® and Joenja® for rare-disease patients based on diagnosis and clinical need.

Hospitals and treatment centers

Administer or coordinate specialty therapies for severe, medically complex cases.

Payers and national health systems

Approve reimbursement and influence access to high-cost orphan medicines.

Specialty pharmacies

Distribute the medicines to patients and support fulfillment of prescriptions.

Strategy

Pharming’s strategy centers on building and commercializing a portfolio of rare-disease medicines, with a focus on expanding use of RUCONEST® and Joenja® and broadening its therapeutic reach. The business also relies on maintaining regulatory, clinical, and commercial execution in multiple markets, where patient identification and reimbursement are key to growth. Portfolio expansion through biologics and small molecules supports longer-term diversification beyond a single product.

Grow the commercial rare-disease portfolioShort term

Commercial medicines are the core revenue engine and support scale in specialty markets.

Broaden the pipeline across biologics and small moleculesMedium term

Diversification reduces reliance on any one therapy and extends the company’s addressable market.

Strengthen global market accessMedium term

Rare-disease products depend on reimbursement, diagnosis, and specialist adoption in each country.

Geography

Pharming is headquartered in Leiden, the Netherlands, and operates across the United States and Europe. The company’s commercial footprint is international, with the U.S. an important market for approved rare-disease medicines and Europe supporting both commercial and corporate operations. Because its products are specialty therapies, access, reimbursement, and regulatory approvals vary by country and can shape market opportunity.

Risks

Pharming’s business is exposed to clinical, regulatory, and commercial risks typical of rare-disease drug developers, including trial outcomes, market access, and competitive therapies. Because revenues depend on a small number of specialty products, adoption, reimbursement, and physician diagnosis rates can materially affect performance. The company also faces execution risk in commercialization and the ongoing need to support its development pipeline.

Sorted by severity
LowMediumHighLowMediumHighImpact →Likelihood →Market access and reimbursement risk1Product concentration risk2Clinical development risk3Regulatory risk4
Impact is the risk’s severity and likelihood how probable it is over the next few years, both assessed from the company’s reports. Numbers match the list.
  1. Market access and reimbursement riskImpact: HighLikelihood: High

    Specialty medicines require payer coverage and country-level reimbursement decisions.

    Exposure: RUCONEST® and Joenja® commercialization

  2. Product concentration riskImpact: HighLikelihood: High

    Revenue depends on a limited number of therapies in narrow patient populations.

    Exposure: Commercial rare-disease portfolio

  3. Clinical development riskImpact: HighLikelihood: Medium

    Pipeline programs depend on successful trial design, enrollment, and data outcomes.

    Exposure: Rare-disease pipeline and new indications

  4. Regulatory riskImpact: MediumLikelihood: Medium

    Approvals, label changes, and post-marketing obligations can affect sales and development timelines.

    Exposure: U.S. and European operations

Accounting

Judgemental items
Revenue recognition

Specialty-drug sales can involve gross-to-net deductions and timing differences between shipment and net revenue.

Impact: Affects reported revenue and margins

Returns and rebates

Payer rebates, discounts, and product returns can materially change net sales in rare-disease markets.

Impact: Affects net revenue and receivables

Intangible assets and development costs

Drug programs may create capitalized assets whose value depends on future commercialization success.

Impact: Affects amortization and impairment risk

Going concern assessment

Management must assess funding for at least the next twelve months in interim reporting.

Impact: Affects disclosure and liquidity analysis

Publicly listed companies with a comparable business focus.

Last updated: 28/09/2026