NEW YORK, Feb. 4, 2021 /PRNewswire/ — Pomerantz LLP is investigating claims on behalf of investors of Sarepta Therapeutics, Inc. (“Sarepta” or the “Enterprise”)(NASDAQ: SRPT).  This kind of investors are advised to make contact with Robert S. Willoughby at  [email protected] or 888-476-6529, ext. 7980.

The investigation concerns no matter if Sarepta and sure of its officers and/or directors have engaged in securities fraud or other illegal business enterprise procedures. 

[Click here for information about joining the class action] 

On January 7, 2021, Sarepta issued a push release asserting prime-line results for Part 1 of the Company’s Research SRP-9001-102 (“Research 102”), “an ongoing, randomized, double-blind, placebo-controlled clinical demo to evaluate the safety, efficacy and tolerability of a one dose of SRP-9001 (rAAVrh74.MHCK7.micro-dystrophin) in 41 people with Duchenne muscular dystrophy. SRP-9001 is an investigational gene transfer treatment meant to supply its micro-dystrophin-encoding gene to muscle mass tissue for the targeted production of the micro-dystrophin protein.”  Whilst Sarepta touted the simple fact that Study 102 met its principal organic endpoint “[a]t 12 months publish-remedy compared to baseline,” the products candidate unsuccessful to coincide with statistically considerable enhancements in muscle mass operate for all individuals immediately after 1 12 months. 

On this news, Sarepta’s inventory cost fell $86.66 for each share, or 51.29%, to shut at $82.29 for each share on January 8, 2021.&#13

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Robert S. Willoughby
Pomerantz LLP
[email protected] 
888-476-6529 ext. 7980

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