– Recipients include 20 individuals living with Duchenne muscular dystrophy and five siblings of individuals living with Duchenne
CAMBRIDGE, Mass.--(BUSINESS WIRE)-- Sarepta Therapeutics, Inc. (NASDAQ:SRPT), the leader in precision genetic medicine for rare diseases, today announced 25 recipients of Route 79, The Duchenne Scholarship Program for the 2023-2024 academic year. Of the 25 recipients, academic scholarships will be awarded to 20 individuals living with Duchenne muscular dystrophy and to five siblings of individuals living with Duchenne. Each recipient will receive a scholarship of up to $5,000.
“On behalf of Sarepta and the selection committee, we are proud to announce the recipients of Route 79, The Duchenne Scholarship Program, for the 2023-2024 academic year. We continue to be impressed by each applicant and this year, we selected a total of 25 exceptionally bright students with passion for growth and a strong vision for their future,” said Diane Berry, Sarepta’s Executive Vice President and Chief Global Policy & Advocacy Officer. “Each student’s essay demonstrated enthusiasm for their academic and life goals, a keen curiosity and admirable desire to learn, and the power of their own perseverance. We are honored to support this ambitious group of students and we wish them great success in their studies for the school year ahead.”
The Route 79 program was created in 2018 to recognize exceptional individuals living with Duchenne as they pursue their post-secondary education. In 2022, Sarepta expanded the program to include siblings of individuals with Duchenne in recognition of the impact that a diagnosis of Duchenne may have on the entire family. Recipients of the scholarship are chosen by an independent selection committee composed of Duchenne community members, who consider each applicant’s community involvement and personal essay. In addition to application review by the independent committee, submissions are de-identified for the voting panel with no indication of whether the candidate has received, or plans to receive, a Sarepta therapy.
2023-2024 Route 79 Scholarship Recipients
John "Jack" Becker, Embry-Riddle Aeronautical University, Daytona Beach
Christopher Cameron, Ball State University
Jacob Colby, The Evergreen State College
Kyle Cox, Texas A&M University
Agranil Das, Stony Brook University
Blake Deakin, Arizona State University
Corbin Fanning, Texas A&M University
Aiden Fecteau, Eastern Connecticut State University
Yuvaraj Gambhir, University of Pennsylvania
Declan Hickey, Curry College
Yujia Ji, The Ohio State University
Elliott Johnson, Lebanon Valley College
Ryan Lugo, State University of New York at New Paltz
Brian Madura, New Jersey Institute of Technology
Josh Pflueger, Texas Christian University
Jasdeep Singh, Cleveland Institute of Art
Vedant Singhania, San Jose State University
Connor Underwood, Pikes Peak State College
Braden Van Eperen, Union College
Jack Wolf, University of Akron
2023-2024 Route 79 Sibling Scholarship Recipients
Hailey Baquiran, Dominican University of California
Ellyn Beebe, University of Tennessee at Martin
Isabel Dreher, University of New Hampshire
Lance Hains, West Chester University
Grace Lee, University of Colorado Boulder
About Route 79, The Duchenne Scholarship Program
The Route 79 program is designed to help students living with Duchenne and siblings of individuals living with Duchenne pursue their post-secondary educational goals. Scholarship recipients are chosen by an independent committee of Duchenne community members based on an applicant’s community involvement, personal essay, and recommendation letter. The underlying cause of Duchenne is a difference in the gene coding for dystrophin. Dystrophin is an essential protein that plays a pivotal role in muscle structure, function and preservation. The numerical significance of the scholarship’s name, Route 79, ties to the 79 exons of the dystrophin gene. For more information, visit sarepta.com/route79.
About Sarepta Therapeutics
Sarepta is on an urgent mission: engineer precision genetic medicine for rare diseases that devastate lives and cut futures short. We hold leadership positions in Duchenne muscular dystrophy (DMD) and limb-girdle muscular dystrophies (LGMDs), and we currently have more than 40 programs in various stages of development. Our vast pipeline is driven by our multi-platform Precision Genetic Medicine Engine in gene therapy, RNA and gene editing. For more information, please visit or follow us on Twitter, LinkedIn, Instagram and Facebook.
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