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Abeona Therapeutics Announces New Employee Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)

Key Takeaway: Abeona Therapeutics Inc. has granted equity awards under Nasdaq Listing Rule 5635(c)(4) to new non-executive employees as an inducement for their employment. The awards total up to 25,500 restricted shares of common stock, vesting over three years. This news comes as Abeona anticipates the FDA's decision on its Biologics License Application for pz-cel, aimed at treating recessive dystrophic epidermolysis bullosa, by May 25, 2024. The company continues to advance its portfolio of gene therapies, particularly for ophthalmic diseases.

Market Sentiment Analysis

POSITIVE FACTORS

  • Abeona granted equity awards to new employees, encouraging talent acquisition.
  • The company is preparing for potential FDA approval on its innovative gene therapy for a rare disease.
  • Abeona's integrated manufacturing facility could support commercial production following FDA approval.

Full Press Release Details

CLEVELAND, March 05, 2024 (GLOBE NEWSWIRE) -- Abeona Therapeutics Inc. (Nasdaq: ABEO) today announced it has granted equity awards to new non-executive employees who joined the Company. The equity awards were approved in accordance with Nasdaq Listing Rule 5635(c)(4).
On February 29, 2024, the Compensation Committee of Abeona’s Board of Directors granted restricted stock equity awards as a material inducement to employment to three individuals hired by Abeona, which equity awards relate to, in the aggregate, up to 25,500 restricted shares of Abeona common stock. One-third of the shares subject to such restricted stock awards will vest yearly on each anniversary of the Grant Date, such that the shares subject to such restricted stock awards granted to each employee will be fully vested on the third anniversary of the Grant Date, in each case, subject to each employee’s continued employment with Abeona on the applicable vesting dates.
About Abeona Therapeutics
Abeona Therapeutics Inc. is a clinical-stage biopharmaceutical company developing cell and gene therapies for serious diseases. The U.S. FDA has accepted and granted Priority Review with a PDUFA target action date of May 25, 2024 for the Biologics License Application for pz-cel (prademagene zamikeracel), Abeona’s investigational autologous, COL7A1 gene-corrected epidermal sheets currently in development for recessive dystrophic epidermolysis bullosa. The Company’s fully integrated cell and gene therapy cGMP manufacturing facility served as the manufacturing site for pz-cel used in its Phase 3 VIITAL™ trial, and is capable of supporting commercial production of pz-cel upon FDA approval. The Company’s development portfolio also features AAV-based gene therapies for ophthalmic diseases with high unmet medical need. Abeona’s novel, next-generation AAV capsids are being evaluated to improve tropism profiles for a variety of devastating diseases. For more information, visit www.abeonatherapeutics.com.
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, the timing and outcome of our Biologics License Application submission to the FDA for pz-cel; the FDA’s grant of a Priority Review Voucher; continued interest in our rare disease portfolio; our ability to enroll patients in clinical trials; the outcome of future meetings with the FDA or other regulatory agencies, including those relating to preclinical programs; the ability to achieve or obtain necessary regulatory approvals; the impact of any changes in the financial markets and global economic conditions; 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 the 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.

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Investor and Media Contact:
VP, Investor Relations and Corporate Communications

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Frequently Asked Questions

What equity awards did Abeona grant recently?

Abeona granted restricted stock equity awards totaling 25,500 shares to new non-executive employees.

When will the restricted stock awards fully vest?

The restricted stock awards will fully vest on the third anniversary of the Grant Date.

What is Abeona Therapeutics known for?

Abeona Therapeutics develops cell and gene therapies for serious diseases.

What is the target action date for Abeona's pz-cel application?

The target action date for the pz-cel application is May 25, 2024.

What does AAV stand for in Abeona's therapies?

AAV stands for adeno-associated virus, used in gene therapies for ophthalmic diseases.

Last updated: Mar 5, 2024