Sarepta Therapeutics Announces Recipients of Route 79, The Duchenne Scholarship Program
Sarepta Therapeutics (NASDAQ:SRPT) announced the recipients of Route 79, The Duchenne Scholarship Program, on World Duchenne Awareness Day. Fifteen individuals living with Duchenne muscular dystrophy will each receive scholarships of up to $5,000 to support their post-secondary education. The selection was made by an independent committee based on community involvement and personal essays. This program aims to support students with Duchenne in their educational pursuits, reflecting Sarepta's commitment to the Duchenne community.
- Awarding scholarships to 15 recipients demonstrates community support and commitment.
- Scholarships of up to $5,000 each can significantly aid in educational pursuits.
- None.
CAMBRIDGE, Mass., Sept. 07, 2021 (GLOBE NEWSWIRE) -- Sarepta Therapeutics, Inc. (NASDAQ:SRPT), the leader in precision genetic medicine for rare diseases, today announced fifteen recipients of Route 79, The Duchenne Scholarship Program. This is the fourth year of the scholarship program, which was created to recognize exceptional individuals living with Duchenne muscular dystrophy as they pursue their post-secondary education. We share this good news on World Duchenne Awareness Day, a day when much of the global community is focused on this year’s special theme ‘Adult Life & Duchenne.’ Recipients of this scholarship were chosen by an independent selection committee composed of Duchenne community members, who consider each applicant’s community involvement and a personal essay. Each student will receive a scholarship of up to
“On behalf of Sarepta and the selection committee it is my pleasure to announce the 2021 recipients of Route 79, The Duchenne Scholarship Program and congratulate them on this achievement. The awardees have shown tremendous determination, resiliency and dedication to their academic pursuits, even in the face of the challenges and disruptions resulting from the ongoing pandemic,” said Diane Berry, Sarepta’s Senior Vice President of Global Health Policy, Government and Patient Affairs. “We are honored to support these young adults in their journey through higher education, and we wish them new opportunities and success in the school year ahead. I also would like to express my appreciation to the selection committee, the members of which gave so generously of their time in reviewing the applications and essays.”
2021 Named Recipients - Route 79, The Duchenne Scholarship Program
Porter Aydelotte, Saddleback College
Brett Dettmer, University of Missouri-Columbia
Billy Ellsworth, Community College of Allegheny County
Aiden Fecteau, Eastern Connecticut State University
Bryson Foster, University of North Carolina at Charlotte
Yuvaraj Gambhir, University of Pennsylvania
Ethan Higginbotham, Wichita State University
Brian Le, Stanford University
Jake Marrazzo, Wheaton College
Darrel Nicklow, Jr., Florida Gulf Coast University
Spencer Poole, Saint Joseph’s College-Suffolk Campus
James Scott, University of San Diego
Parker Strobeck, North Arkansas College
Tayjus Surampudi, Harvard University
Joseph Ware, Liberty University
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.
About Route 79, The Duchenne Scholarship Program
Route 79, The Duchenne Scholarship Program is designed to help students diagnosed with Duchenne muscular dystrophy (Duchenne) pursue their post-high school educational goals. There are 79 exons in the dystrophin gene impacted by Duchenne, and the route traveled by every person with Duchenne is distinct. Sarepta’s goal through this program is to acknowledge and support individuals with Duchenne who are mapping out their future via educational pursuits. Additional information is available at https://www.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 www.sarepta.com or follow us on Twitter, LinkedIn, Instagram and Facebook.
Internet Posting of Information
We routinely post information that may be important to investors in the 'For Investors' section of our website at www.sarepta.com. We encourage investors and potential investors to consult our website regularly for important information about us.
Source: Sarepta Therapeutics, Inc.
Investor Contact:
Ian Estepan, 617-274-4052
iestepan@sarepta.com
Media Contact:
Tracy Sorrentino, 617-301-8566
tsorrentino@sarepta.com
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