ZEALNasdaq CopenhagenBiotechnologyIFRS · DKK

Zealand Pharma A/S

Zealand Pharma A/S is a Danish biopharmaceutical company focused on discovering and developing peptide-based medicines. Its portfolio centers on drug candidates for metabolic and gastrointestinal diseases, with programs advanced through internal R&D and collaboration agreements.

Revenue9,215m DKK
+14,598.9 %y/y
Operating profit (EBIT)6,959m DKK
+647.0 %y/y
EBIT margin75.5%
+2,104.9 ppy/y
Net income6,455m DKK
+698.3 %y/y
Free cash flow6,499m DKK
+790.7 %y/y

Fiscal year 2025 · change from previous year

Development 2021–2025

-2,50002,5005,0007,50010,000m DKK2021: 239 m DKK2021: EBIT -763 m DKK20212022: 104 m DKK2022: EBIT -837 m DKK20222023: 343 m DKK2023: EBIT -572 m DKK20232024: 63 m DKK2024: EBIT -1,272 m DKK20242025: 9,215 m DKK2025: EBIT 6,959 m DKK2025TTM 2026: 4,643 m DKKTTM 2026: EBIT 2,348 m DKKTTM4,6432,348
RevenueOperating profit (EBIT)TTM = last 12 months, not a full fiscal year

Business

Share of revenue
Peptide drug candidates70 %

Clinical and preclinical peptide-based medicines for metabolic and gastrointestinal diseases.

Collaboration revenue25 %

Upfront, milestone, and cost-reimbursement revenue from partner agreements.

License rights and development assets5 %

Capitalized rights to co-develop or commercialize partnered drug candidates.

Customers

Zealand Pharma sells primarily to pharmaceutical partners rather than end patients, with value created through licensing, co-development, and milestone-bearing collaboration agreements. Its commercial counterparties are large biopharma companies that fund development, share costs, and may commercialize products after approval. The underlying end markets are patients and healthcare systems that use treatments for obesity and other chronic metabolic conditions.

Pharmaceutical collaboration partners

Buy development rights, share costs, and pay milestones for Zealand's peptide programs.

Licensing and co-commercialization partners

Access specific assets and commercialization rights under structured agreements.

Healthcare end users

Patients treated with approved obesity or gastrointestinal therapies developed from the pipeline.

Strategy

Zealand Pharma's strategy is centered on advancing peptide medicines through partnered development, which allows it to share cost, scientific risk, and commercial upside. The Roche collaboration shows the importance of building combination products and milestone-rich agreements that can fund pipeline advancement and broaden eventual commercialization potential.

Advance key obesity and metabolic programsShort term

Late-stage clinical progress is essential for future milestones, approvals, and commercial value.

Execute partnered co-development agreementsMedium term

Partnerships provide funding, validation, and access to commercialization infrastructure.

Expand monetization through milestones and royaltiesLong term

Structured payments diversify funding and create upside tied to clinical and sales success.

Geography

The company is headquartered in Denmark and operates as a global biopharma developer through international collaborations rather than a broad manufacturing footprint. Its reported revenue exposure is shaped by partnership agreements that can generate royalties and milestones across the U.S., Europe, and other markets. Geography matters mainly through where partners commercialize products and where development activities, payments, and currency exposures arise.

Risks

The business is highly dependent on clinical success, regulatory outcomes, and partner execution, so setbacks can materially affect future revenue and asset values. It also faces concentration risk in a small number of collaboration agreements, together with foreign exchange and valuation risk from milestone structures, derivative contracts, and capitalized intangible assets.

Sorted by severity
LowMediumHighLowMediumHighImpact →Likelihood →Partner concentration1Clinical development failure2Intangible asset impairment3Foreign exchange volatility4
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. Partner concentrationImpact: HighLikelihood: High

    A large share of economics is tied to a limited number of collaboration agreements.

    Exposure: Roche and other strategic partners

  2. Clinical development failureImpact: HighLikelihood: Medium

    Pipeline value depends on positive trial results and progression to later stages.

    Exposure: Petrelintide and other development programs

  3. Intangible asset impairmentImpact: HighLikelihood: Medium

    Capitalized license rights depend on continued clinical and commercial viability.

    Exposure: CT-388 license rights and related development assets

  4. Foreign exchange volatilityImpact: MediumLikelihood: High

    Milestones and receivables are linked to USD amounts while reporting is in DKK.

    Exposure: USD milestone receipts and FX forwards

Accounting

Judgemental items
Revenue recognition for collaboration agreements

Upfront payments, milestones, and reimbursed development costs follow different recognition patterns.

Impact: Can create large, uneven revenue recognition across periods

Intangible asset capitalization

License installments for CT-388 are recorded as intangible assets as contractual payments become due.

Impact: Affects balance sheet size and future impairment risk

Fair value of derivatives

FX forwards and warrant-related instruments are remeasured through earnings.

Impact: Introduces volatility in financial items

Contract assets and trade receivables

Development milestones and cost-sharing balances may be invoiced later than recognition.

Impact: Affects working capital and reported revenue timing

Publicly listed companies with a comparable business focus.

Last updated: 24/10/2026