Press Releases May 4, 2026 08:30 AM

Abeona Therapeutics® Announces Date of First Quarter Financial Results

Abeona Therapeutics schedules Q1 2026 financial results call amid ongoing gene therapy developments

By Caleb Monroe ABEO
Abeona Therapeutics® Announces Date of First Quarter Financial Results
ABEO

Abeona Therapeutics Inc., a commercial-stage biopharmaceutical company specializing in cell and gene therapies, announced its first quarter 2026 financial results conference call to be held on May 13, 2026. The company highlighted its commercial product ZEVASKYN, a gene therapy for recessive dystrophic epidermolysis bullosa, and its ongoing pipeline of AAV-based gene therapies for ophthalmic diseases. The announcement included forward-looking statements about commercialization, regulatory approval, and market opportunities.

Key Points

  • Abeona will host a conference call on May 13, 2026, to discuss Q1 financial results and corporate progress.
  • The company commercializes ZEVASKYN, the first autologous cell-based gene therapy for RDEB wounds, manufactured in their Cleveland facility.
  • Abeona has a pipeline of AAV-based gene therapies targeting serious ophthalmic diseases with high unmet medical needs.

CLEVELAND, May 04, 2026 (GLOBE NEWSWIRE) -- Abeona Therapeutics Inc. (Nasdaq: ABEO) today announced it will host a conference call on Wednesday, May 13, 2026 at 8:30 a.m. ET to discuss its financial results for the first quarter of 2026 and corporate progress.

The conference call will be available via phone and webcast. To access the call, dial 888-506-0062 (U.S. toll-free) or 973-528-0011 (international) and Entry Code: 305519 five minutes prior to the start of the call. A live, listen-only webcast and archived replay of the call can be accessed on the Investors & Media section of Abeona’s website at https://investors.abeonatherapeutics.com/events. The archived webcast replay will be available for 30 days following the call.

About Abeona Therapeutics

Abeona Therapeutics Inc. is a commercial-stage biopharmaceutical company developing cell and gene therapies for serious diseases. Abeona’s ZEVASKYN® (prademagene zamikeracel) is the first and only autologous cell-based gene therapy for the treatment of wounds in adults and pediatric patients with recessive dystrophic epidermolysis bullosa (RDEB). The Company’s fully integrated cell and gene therapy cGMP manufacturing facility in Cleveland, Ohio serves as the manufacturing site for ZEVASKYN commercial production. The Company’s development portfolio features adeno-associated virus (AAV)-based gene therapies for ophthalmic diseases with high unmet medical need. Abeona’s novel, next-generation AAV capsids are being evaluated for a variety of devastating diseases. For more information, visit www.abeonatherapeutics.com.

ZEVASKYN®, Abeona Assist®, Abeona Therapeutics®, and their related logos are trademarks of Abeona Therapeutics Inc.

Forward-Looking Statements

This press release contains certain statements that are forward-looking within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, and that involve risks and uncertainties. We have attempted to identify forward-looking statements by such terminology as “may,” “will,” “believe,” “anticipate,” “expect,” “intend,” “potential,” and similar words and expressions (as well as other words or expressions referencing future events, conditions or circumstances), which constitute and are intended to identify forward-looking statements. Actual results may differ materially from those indicated by such forward-looking statements as a result of various important factors, numerous risks and uncertainties, including but not limited to, our ability to successfully commercialize and market ZEVASKYN, including manufacturing sufficient batches of ZEVASKYN to meet demand; the therapeutic potential of ZEVASKYN; whether the unmet need and market opportunity for ZEVASKYN are consistent with the Company’s expectations; continued interest in our rare disease portfolio; our ability to enroll patients in clinical trials; the outcome of future meetings with and inspections by the FDA or other regulatory agencies, including those relating to preclinical programs and to the cGMP manufacturing of ZEVASKYN; the ability to achieve or obtain necessary regulatory approvals for our pre-clinical programs; the impact of any changes in the financial markets and global economic conditions, including those resulting from changes to U.S. trade policy, such as current or future tariffs; risks associated with data analysis and reporting; and other risks disclosed in the Company’s most recent Annual Report on Form 10-K and subsequent periodic reports filed with the Securities and Exchange Commission. The Company undertakes no obligation to revise these forward-looking statements or to update them to reflect events or circumstances occurring after the date of this press release, whether as a result of new information, future developments or otherwise, except as required by the federal securities laws.

Contacts:

Investor and Media
Greg Gin
VP, Investor Relations and Corporate Communications
Abeona Therapeutics
[email protected]

Investor
Lee M. Stern
Meru Advisors
[email protected]


Risks

  • Uncertainty in commercializing and marketing ZEVASKYN, including manufacturing capacity risks.
  • Regulatory risks related to FDA inspections, approvals for current and preclinical programs.
  • Market risks tied to financial market conditions and potential changes in U.S. trade policies affecting operations.

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