Abeona Therapeutics Inc

Research Abeona Therapeutics Inc (ABEO) on Bullrun: market cap USD 282.70M. Explore financials, valuation history, model signals, and stock context.

Key Metrics

Valuation Snapshot

latest market cap is USD 282.70M.

Five-year financial history

YearRevenueNet incomeFree cash flowGross marginDiluted EPSCashTotal debtEquity
FY2025USD 5.82M-USD 71.18M-USD 84.30M73.7%1.01USD 78.44MUSD 20.04MUSD 159.22M
FY2024USD 0USD 63.73M-USD 58.46Mn/a-1.55USD 23.36MUSD 18.96MUSD 44.03M
FY2023USD 3.50MUSD 54.19M-USD 37.34M54.1%-2.53USD 14.47MUSD 5.40MUSD 14.83M
FY2022USD 1.41M-USD 39.70M-USD 43.61M68.2%-5.53USD 14.22MUSD 7.63MUSD 26.76M

Valuation history

YearSnapshot dateMarket capP/EDividend yieldAnnual dividend/share
20262026-10-09USD 282.70Mn/an/an/a
20252025-12-31USD 290.08M5.3n/an/a
20242024-12-31USD 254.24Mn/an/an/a
20232023-12-29USD 124.11Mn/an/an/a
20222022-12-30USD 52.90Mn/an/an/a
20212021-12-31USD 50.05Mn/an/an/a

About Abeona Therapeutics Inc

Abeona Therapeutics Inc., a commercial-stage biopharmaceutical company, develops gene and cell therapies for life-threatening diseases in the United States. It develops ZEVASKYN, an autologous, cell-based gene therapy for the treatment of patients with recessive dystrophic epidermolysis bullosa. The company also develops ABO-503 to treat X-linked retinoschisis; ABO-504 for the treatment of stargardt disease; and ABO-505 to treat autosomal dominant optic atrophy.

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Frequently asked questions

What is Abeona Therapeutics Inc's market cap?

Abeona Therapeutics Inc's market capitalization is USD 282.70M.

What does Abeona Therapeutics Inc do?

Abeona Therapeutics Inc., a commercial-stage biopharmaceutical company, develops gene and cell therapies for life-threatening diseases in the United States. It develops ZEVASKYN, an autologous, cell-based gene therapy for the treatment of patients with recessive dystrophic epidermolysis bullosa. The company also develops ABO-503 to treat X-linked retinoschisis; ABO-504 for the treatment of stargardt disease; and ABO-505 to treat autosomal dominant optic atrophy. In addition, it is developing AAV-based gene therapy through its AIM vector platform programs.