Sarepta Therapeutics Announces Inducement Grants Under Nasdaq Rule 5635(c)(4)

Sarepta Therapeutics, Inc. (NASDAQ: SRPT), a global leader in precision genetic medicine for rare diseases, announced on November 29, 2024, the granting of equity awards to 14 new employees who joined the company in November 2024. These equity awards, which were approved by Sarepta’s Compensation Committee under the 2024 Employment Commencement Incentive Plan, were provided as a material inducement to their employment. This grant was made in accordance with Nasdaq Listing Rule 5635(c)(4), which outlines the conditions for equity awards granted to new employees as part of their hiring process.

In total, the 14 employees were awarded 8,040 restricted stock units (RSUs). The RSUs are subject to a vesting schedule, with one-fourth of the granted units vesting each year on the anniversary of the Grant Date. This means that the RSUs granted to each employee will become fully vested by the fourth anniversary of the Grant Date, as long as the employee remains employed with Sarepta on each respective vesting date. Importantly, no options to purchase shares of Sarepta’s common stock were granted as part of this equity award package. The RSUs are intended to align the interests of new employees with those of the company and reward their contributions over time, helping to retain key talent within the organization.

This equity award is part of Sarepta’s ongoing strategy to attract and retain top talent as it advances its mission to develop groundbreaking genetic therapies for rare diseases. By offering competitive inducement packages to new hires, Sarepta demonstrates its commitment to ensuring the company remains at the forefront of innovation in the field of precision genetic medicine.

About Sarepta Therapeutics

Sarepta Therapeutics is an innovative biotechnology company focused on developing precision genetic medicine to treat rare, serious diseases that currently have limited treatment options. The company’s mission is critical, as it aims to engineer therapies that can fundamentally change the lives of patients living with genetic disorders that are often debilitating and life-limiting.

Sarepta is widely recognized as a leader in the field of gene therapy for rare diseases, particularly for Duchenne muscular dystrophy (DMD) and limb-girdle muscular dystrophies (LGMDs). These rare, genetic diseases lead to progressive muscle weakness and can significantly reduce life expectancy. Sarepta has made remarkable progress in developing treatments for DMD, an inherited muscle-wasting disorder, and is working on therapies for other forms of muscular dystrophy, including LGMDs, which also have a significant unmet medical need.

In addition to its work in muscular dystrophies, Sarepta is advancing a broad and diverse pipeline of over 40 programs targeting genetic diseases across various therapeutic areas. The company’s pipeline spans gene therapy, RNA-based therapies, and gene editing, positioning it as a pioneer in the rapidly growing field of precision medicine. Sarepta’s innovative approach is centered on its multi-platform Precision Genetic Medicine Engine, which combines cutting-edge technology in gene therapy, RNA manipulation, and gene editing to develop highly targeted treatments for rare genetic disorders.

The company’s focus on precision genetic medicine allows it to design therapies that are tailored to address the specific genetic mutations that cause these diseases, offering hope to patients who have long lacked effective treatment options. By leveraging its expertise and technological capabilities, Sarepta aims to not only treat these diseases but also to potentially cure them, offering patients a chance for a better quality of life and improved long-term outcomes.

Sarepta’s commitment to innovation and patient-centered care has earned it a leadership position in the field, and the company continues to push the boundaries of what is possible in genetic medicine. With a growing pipeline of promising therapies and a strong focus on bringing new treatments to market, Sarepta is poised to continue its vital work in transforming the landscape of rare disease treatment.

Through its strategic initiatives, such as the recent equity awards granted to new employees, Sarepta also demonstrates its commitment to building a team of experts who are dedicated to advancing the company’s mission. By investing in its workforce, Sarepta is positioning itself for continued success in its efforts to revolutionize the treatment of rare genetic diseases.

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