Sarepta Therapeutics to Present at the 40th Annual J.P. Morgan Healthcare Conference

Rhea-AI Summary

Sarepta Therapeutics (NASDAQ:SRPT) will present at the 40th Annual J.P. Morgan Healthcare Conference on January 10, 2022, showcasing topline results from Part 2 of Study SRP-9001-102. This study focuses on the investigational gene therapy SRP-9001 for children aged 4 to 7 with Duchenne muscular dystrophy. The virtual presentation is scheduled for 10:30 a.m. E.T. and will include a Q&A session. The event can be accessed live on Sarepta's investor relations website, where it will also be archived for 90 days.

• Presentation on Monday, Jan. 10, 2022, to include topline results from Part 2 of Study SRP-9001-102

CAMBRIDGE, Mass., Jan. 06, 2022 (GLOBE NEWSWIRE) -- Sarepta Therapeutics, Inc. (NASDAQ:SRPT), the leader in precision genetic medicine for rare diseases, today announced that senior management will present virtually at the 40th Annual J.P. Morgan Healthcare Conference on Monday, Jan. 10, 2022 at 10:30 a.m. E.T. / 7:30 a.m. P.T. Following the presentation there will be a Q&A session starting at 10:50 a.m. E.T. / 7:50 a.m. P.T.

In addition to a general corporate update, Sarepta will share topline results from Part 2 of Study SRP-9001-102 (Study 102), a double-blind, 1:1 randomized, placebo-controlled clinical trial of SRP-9001 in 41 participants with Duchenne muscular dystrophy between the ages of 4 to 7 at time of treatment. SRP-9001 (delandistrogene moxeparvovec) is an investigational gene transfer therapy intended to deliver its micro-dystrophin-encoding gene to muscle tissue for the targeted production of the micro-dystrophin protein.

The presentation and Q&A session will be webcast live under the Events & Presentations section of investor relations section of Sarepta’s website at https://investorrelations.sarepta.com/events-presentations and will be archived there following the presentation for 90 days. Please connect to Sarepta's website several minutes prior to the start of the broadcast to ensure adequate time for any software download that may be necessary.

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

FAQ

What are the topline results from Study SRP-9001-102 by Sarepta Therapeutics?

Sarepta will present topline results from Part 2 of Study SRP-9001-102 at the J.P. Morgan Healthcare Conference on January 10, 2022.

When is Sarepta Therapeutics' presentation at the J.P. Morgan Healthcare Conference?

Sarepta's presentation is scheduled for January 10, 2022, at 10:30 a.m. E.T.

What is SRP-9001 in relation to Duchenne muscular dystrophy?

SRP-9001 is an investigational gene therapy aimed at delivering a micro-dystrophin-encoding gene for treating Duchenne muscular dystrophy.

How can I watch Sarepta Therapeutics' presentation at the conference?

The presentation will be webcast live on Sarepta’s investor relations website and archived for 90 days.

What does Sarepta Therapeutics' pipeline include?

Sarepta focuses on precision genetic medicine for rare diseases, with over 40 programs in various stages of development.