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Sarepta Therapeutics to Report 3-Year Topline Data from EMBARK Study of ELEVIDYS Gene Therapy in Ambulatory Individuals with Duchenne Muscular Dystrophy

Key Takeaway: Sarepta Therapeutics will present 3-year topline data from the EMBARK study on January 26, 2026. This Phase 3 study evaluates the efficacy of ELEVIDYS gene therapy in young patients with Duchenne muscular dystrophy. The event will be accessible via a live webcast and will include a replay for later viewing.
Price reaction · baseline $21.13 (2026-01-23 close) · hit pre-market · 2 other SRPT headline(s) in the window, move may be shared
day 0 close · peak
+7.9%
day 1
+4.9%
day 3
+0.5%

Market Sentiment Analysis

POSITIVE FACTORS

  • Sarepta is presenting promising 3-year data from the EMBARK study.
  • The study focuses on a significant treatment for Duchenne muscular dystrophy.
  • The company is a leader in precision genetic medicine.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+46%
120-day peak, hindsight
Typical move
16.8%
average across 4 past catalysts
Lead asset
Eteplirsen
Phase 3 · Muscular Dystrophy, Duchenne

Full Press Release Details

CAMBRIDGE, Mass.--(BUSINESS WIRE)--Sarepta Therapeutics, Inc. (NASDAQ:SRPT), the leader in precision genetic medicine for rare diseases, today announced that on Monday, Jan. 26, 2026, at 8:30 am Eastern Time, the Company will host a webcast and conference call to present 3-year topline functional results from patients treated in Part 1 of EMBARK (Study 9001-301), the global, randomized placebo-controlled Phase 3 study evaluating ELEVIDYS (delandistrogene moxeparvovec-rokl) in ambulatory individuals with Duchenne muscular dystrophy who were aged four to seven at time of treatment.
The event will be webcast live under the investor relations section of Sarepta's website athttps://investorrelations.sarepta.com/events-presentationsand following the event a replay will be archived there for one year. Interested parties participating by phone will need to register usingthis online form. After registering for dial-in details, all phone participants will receive an auto-generated e-mail containing a link to the dial-in number along with a personal PIN number to use to access the event by phone.
About Sarepta TherapeuticsSarepta 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 (Duchenne) and are building a robust portfolio of programs across muscle, central nervous system, and cardiac diseases.
Internet Posting of InformationWe routinely post information that may be important to investors in the 'For Investors' section of our website atwww.sarepta.com. We encourage investors and potential investors to consult our website regularly for important information about us.

Frequently Asked Questions

What is the EMBARK study?

The EMBARK study is a Phase 3, randomized placebo-controlled trial evaluating ELEVIDYS in young patients with Duchenne muscular dystrophy.

When will the topline data be presented?

The topline data will be presented on January 26, 2026, at 8:30 am Eastern Time.

How can I access the webcast?

The webcast will be available on Sarepta's investor relations website.

What age group is involved in the study?

The study involves ambulatory individuals aged four to seven at the time of treatment.

Last updated: Jan 26, 2026