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Intrinsic ValueHansa Biopharma AB (publ) (0RC7.L)

Previous Close£84.70
Intrinsic Value
Upside potential
Previous Close
£84.70

VALUATION INPUT DATA

This valuation is based on fiscal year data as of 2024 and quarterly data as of .

Data is not available at this time.

Stock Valuation Context

Business Model And Market Position

Hansa Biopharma AB is a Sweden-based biopharmaceutical company specializing in immunomodulatory treatments for transplant patients and rare IgG-mediated autoimmune conditions. Its proprietary enzyme technology platform underpins therapies targeting high-need areas such as kidney transplantation, autoimmune diseases, and oncology. The company's lead candidate, Imlifidase, is in advanced clinical trials for sensitized kidney transplant patients and anti-GBM antibody disease, positioning Hansa as a potential pioneer in antibody-cleaving therapies. Beyond Imlifidase, Hansa is developing next-generation enzyme therapies like NiceR and EnzE, which aim to expand its pipeline into repeat dosing for chronic conditions and cancer immunotherapy. Collaborations, such as its preclinical research partnership with argenx BV, further validate its technological approach. Operating in the competitive biotechnology sector, Hansa focuses on niche, high-barrier indications where unmet medical needs justify premium pricing. Its market position hinges on successful clinical execution and regulatory approvals, which could establish it as a leader in enzyme-based immunomodulation.

Revenue Profitability And Efficiency

Hansa Biopharma reported revenue of SEK 171.3 million in the latest fiscal year, reflecting its early-stage commercialization efforts. However, the company remains unprofitable, with a net loss of SEK -807.2 million and diluted EPS of SEK -12.84, driven by high R&D expenditures. Operating cash flow was negative SEK -674.9 million, underscoring the capital-intensive nature of its clinical-stage operations. Capital expenditures were minimal at SEK -116,000, indicating a lean asset-light model focused on intellectual property and clinical development.

Earnings Power And Capital Efficiency

The company's earnings power is currently constrained by its pre-revenue status in key programs, with losses amplified by clinical trial costs. Capital efficiency metrics are challenging due to negative cash flows, though its SEK 405.3 million cash reserve provides near-term runway. The high beta of 1.648 reflects market sensitivity to clinical milestones and binary regulatory outcomes.

Balance Sheet And Financial Health

Hansa's balance sheet shows SEK 405.3 million in cash and equivalents against total debt of SEK 1.08 billion, indicating leveraged financing for R&D. The debt load, coupled with persistent operating losses, raises liquidity risks unless additional funding or partnership revenues materialize. Equity financing or strategic collaborations may be necessary to sustain operations beyond the current cash position.

Growth Trends And Dividend Policy

Growth hinges on clinical progress, with Imlifidase's phase 3 data as a near-term catalyst. Revenue growth is expected to remain volatile until commercialization scales. The company does not pay dividends, reinvesting all capital into pipeline development. Future revenue streams will depend on regulatory approvals and market adoption of its enzyme therapies.

Valuation And Market Expectations

With a market cap of SEK 1.62 billion, Hansa trades as a high-risk, high-reward biotech bet. Valuation reflects optimism around its platform's potential, though skepticism persists given its cash burn and unproven commercial viability. The stock's volatility aligns with its clinical-stage profile and binary event-driven nature.

Strategic Advantages And Outlook

Hansa's strategic edge lies in its first-mover potential in antibody-cleaving enzymes, with Imlifidase addressing critical gaps in transplant and autoimmune care. Success in ongoing trials could unlock partnerships or buyout interest. However, execution risks—including trial failures, regulatory hurdles, and funding needs—remain key challenges. The outlook is contingent on clinical and regulatory milestones in 2024-2025.

Sources

Company filings, London Stock Exchange disclosures

show cash flow forecast

FINANCIAL STATEMENTS FORECAST and PRESENT VALUE CALCULATION

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