Either you have JavaScript disabled or your browser does not support Javascript . To work properly, this page requires JavaScript to be enabled.
How to enable JavaScript in your browser?

A multi-center, double blind, placebo-controlled, multi-dose efficacy study of SRP-5051 to evaluate dystrophin expression and clinical outcomes

Next Previous
X
Search
Trial Profile

A multi-center, double blind, placebo-controlled, multi-dose efficacy study of SRP-5051 to evaluate dystrophin expression and clinical outcomes

Status: Planning
Phase of Trial: Phase II

Latest Information Update: 14 Nov 2017

Price :

$35 *

Note:
  • Adis is an information provider.
  • Final gross price and currency may vary according to local VAT and billing address.
  • Your purchase entitles you to full access to the information contained in our trial profile at the time of purchase.
  • A link to download a PDF version of the trial profile will be included in your email receipt.

At a glance

  • Drugs SRP-5051 (Primary)
  • Indications Duchenne muscular dystrophy
  • Focus Therapeutic Use

    • Most Recent Events

    • 14 Nov 2017 New trial record
    • 07 Nov 2017 According to a Sarepta Therapeutics media release, the company is planning to initiate this trial based on the results of a Phase I/II trial (see profile 290305) by mid-year 2018 or as soon as a therapeutic dose has been identified.

You need to be a logged in or subscribed to view this content Request demo

If your organization or you do not have a subscription, try one of the following:
  • Contacting your organization’s admin about adding this content to your AdisInsight subscription
  • Buying a PDF version of any individual profile
  • Request a free trial
If your organization has a subscription, there are several access options, even while working remotely:
  • Working within your organization’s network
  • with username/password or try to via your institution
  • Persisted access using your organization’s identifier stored in your user browser for 90 days
Back to top