Oxford BioMedica PLC

Research Oxford BioMedica PLC (OXB) on Bullrun: market cap GBX 636.66M. Explore financials, valuation history, model signals, and stock context.

Key Metrics

Valuation Snapshot

latest market cap is GBX 636.66M.

Five-year financial history

YearRevenueNet incomeFree cash flowGross marginDiluted EPSCashTotal debtEquity
FY2025GBP 168.74M-GBP 30.13M-GBP 4.25M39.1%-26.92GBP 96.88MGBP 148.13MGBP 91.35M
FY2024GBP 128.80M-GBP 43.19M-GBP 58.16M41.2%-41.75GBP 60.65MGBP 108.76MGBP 57.05M
FY2023GBP 89.54M-GBP 157.49M-GBP 38.35M44.4%-1.63GBP 103.72MGBP 111.46MGBP 74.01M
FY2022GBP 139.99M-GBP 39.16M-GBP 28.91M49.4%-0.41GBP 141.29MGBP 114.28MGBP 204.65M
FY2021GBP 142.80MGBP 19.01MGBP 15.99M57.9%0.22GBP 108.94MGBP 0GBP 187.34M

Valuation history

YearSnapshot dateMarket capP/EDividend yieldAnnual dividend/share
20262026-08-23GBX 636.66Mn/an/an/a

About Oxford BioMedica PLC

Oxford Biomedica plc, a contract development and manufacturing organization, focuses on delivering therapies to patients worldwide. Its LentiVector platform technology is a lentiviral vector based gene delivery system which is designed to overcome the safety and delivery problems associated with earlier generations of vector systems; InAAVate, a proprietary ‘plug and play' dual-plasmid system for transient transfection, as well as a standard triple transfection system for AAV-based gene therapies.

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Frequently asked questions

What is Oxford BioMedica PLC's market cap?

Oxford BioMedica PLC's market capitalization is GBX 636.66M.

What does Oxford BioMedica PLC do?

Oxford Biomedica plc, a contract development and manufacturing organization, focuses on delivering therapies to patients worldwide. Its LentiVector platform technology is a lentiviral vector based gene delivery system which is designed to overcome the safety and delivery problems associated with earlier generations of vector systems; InAAVate, a proprietary ‘plug and play' dual-plasmid system for transient transfection, as well as a standard triple transfection system for AAV-based gene therapies.