VICONasdaq StockholmHealth CareIFRS · SEK

Vicore Pharma Holding

Vicore Pharma Holding AB is a Swedish biopharmaceutical group focused on developing therapies for severe fibrotic diseases. The group operates through Vicore Pharma AB and Vicore Pharma US Inc., with research and development centered in Sweden and supporting activities in the United States.

Revenue0.0m SEK
−100.0 %y/y
Operating profit (EBIT)-0.5m SEK
+99.8 %y/y
EBIT margin-11,851.9%
−11,674.3 ppy/y
Net income-169m SEK
+45.8 %y/y

Fiscal year 2025 · change from previous year

Development 2020–2025

-400-300-200-1000100200m SEK2020: 3.7 m SEK20202021: 0.00 m SEK2021: EBIT -295 m SEK20212022: 0.00 m SEK2022: EBIT -291 m SEK20222023: 0.00 m SEK2023: EBIT -322 m SEK20232024: 109 m SEK2024: EBIT -194 m SEK20242025: 0.00 m SEK2025: EBIT -0.45 m SEK20250.00-0.45
RevenueOperating profit (EBIT)

Business

Share of revenue
Drug discovery and preclinical R&D0 %

Discovery-stage work and early research on therapies for fibrotic diseases.

Clinical development0 %

Human clinical study programs advancing Vicore's fibrosis pipeline.

Research collaborations100 %

Contract-based collaboration income tied to agreed research milestones and performance obligations.

Intra-group services0 %

R&D and business support services provided within the Vicore group.

Customers

Vicore's external counterparties are primarily pharmaceutical partners and research collaborators that fund or participate in development agreements. The company also serves internal group entities through intercompany R&D and business support arrangements, while the ultimate end beneficiaries are patients with severe fibrotic diseases.

Research collaboration partners

Pharmaceutical or biotech partners that pay for or co-develop research programs under contract terms.

Clinical development ecosystem

Clinical sites, CROs, and trial partners that support patient recruitment, study execution, and data generation.

Internal group entities

Vicore Pharma AB and Vicore Pharma US Inc. receive shared services and intra-group R&D support.

Patients with fibrotic diseases

The intended end users of Vicore's therapies, especially in severe fibrosis indications.

Strategy

Vicore's strategy is centered on advancing a pipeline for severe fibrotic diseases through research, clinical development, and external collaborations. The company also relies on partner-enabled development and support functions to extend its capabilities while keeping the organization focused on its core therapeutic programs.

Advance the fibrosis pipelineMedium term

Clinical progress is the main driver of value creation in a development-stage biopharma model.

Strengthen external collaborationsShort term

Partner agreements can provide funding, expertise, and development support.

Rely on outsourced development capabilitiesMedium term

Clinical trials, manufacturing, and supply are partly partner-dependent and require operational resilience.

Geography

Vicore is headquartered in Sweden and conducts core research and development primarily through Vicore Pharma AB. The group also has Vicore Pharma US Inc. in the United States, which supports R&D and business functions and introduces foreign-currency exposure through its assets and liabilities.

Risks

Vicore is exposed to the typical risks of a development-stage biopharmaceutical company: clinical failure, patient recruitment delays, manufacturing issues, and regulatory uncertainty. It also faces partner concentration, supply-chain, foreign-exchange, liquidity, and intellectual-property risks because value depends on successful development and protection of future therapies.

Sorted by severity
LowMediumHighLowMediumHighImpact →Likelihood →Clinical development failure1Patient recruitment and trial execution delays2Intellectual property risk3Foreign exchange and liquidity risk5
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. Clinical development failureImpact: HighLikelihood: High

    Most drug candidates do not reach market due to efficacy, safety, or manufacturing issues.

    Exposure: Pipeline value and future commercialization prospects

  2. Patient recruitment and trial execution delaysImpact: HighLikelihood: Medium

    Studies can be delayed by difficulty recruiting patients or retaining them through follow-up.

    Exposure: Clinical timelines and development costs

  3. Intellectual property riskImpact: HighLikelihood: Medium

    Future value depends on patents and other exclusivity protections that may be limited or challenged.

    Exposure: Commercialization and competitive moat

  4. Partner and supply-chain dependenceImpact: High

    Vicore relies on third parties for trials, manufacturing, and supply, creating operational and quality risk.

    Exposure: Clinical operations and product readiness

  5. Foreign exchange and liquidity riskImpact: MediumLikelihood: Medium

    Costs and agreements are often denominated in foreign currencies and development is capital intensive.

    Exposure: Cash planning and reported translation effects

Accounting

Judgemental items
Over-time revenue recognition for research collaborations

Revenue depends on contract terms and degree of completion, which affects timing and comparability.

Impact: Collaboration income

Foreign currency translation

US subsidiary assets, equity, and liabilities are translated into SEK, creating OCI volatility.

Impact: Other comprehensive income and equity

Tax loss carryforwards

Large accumulated losses are not recognized as deferred tax assets until future taxable profits are expected.

Impact: Deferred tax assets and equity

IFRS 18 presentation changes

New operating/investing/financing categories and MPM disclosures will change statement presentation.

Impact: Income statement presentation and comparability

Publicly listed companies with a comparable business focus.

Last updated: 24/09/2026