Italia markets closed
  • FTSE MIB

    24.095,00
    +29,95 (+0,12%)
     
  • Dow Jones

    31.261,90
    +8,77 (+0,03%)
     
  • Nasdaq

    11.354,62
    -33,88 (-0,30%)
     
  • Nikkei 225

    26.739,03
    +336,19 (+1,27%)
     
  • Petrolio

    110,35
    +0,46 (+0,42%)
     
  • BTC-EUR

    27.742,47
    -1.211,62 (-4,18%)
     
  • CMC Crypto 200

    650,34
    -23,03 (-3,42%)
     
  • Oro

    1.845,10
    +3,90 (+0,21%)
     
  • EUR/USD

    1,0562
    -0,0026 (-0,24%)
     
  • S&P 500

    3.901,36
    +0,57 (+0,01%)
     
  • HANG SENG

    20.717,24
    +596,56 (+2,96%)
     
  • Euro Stoxx 50

    3.657,03
    +16,48 (+0,45%)
     
  • EUR/GBP

    0,8455
    -0,0026 (-0,30%)
     
  • EUR/CHF

    1,0288
    -0,0006 (-0,06%)
     
  • EUR/CAD

    1,3556
    -0,0013 (-0,09%)
     

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

·2 minuto per la lettura
  • 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


Il nostro obiettivo è creare un luogo sicuro e coinvolgente in cui gli utenti possano entrare in contatto per condividere interessi e passioni. Per migliorare l’esperienza della nostra community, sospendiamo temporaneamente i commenti sugli articoli