Trial record 3 of 3 for:
SRP-5051
Two-Part Study for Dose Determination of Vesleteplirsen (SRP-5051) (Part A), Then Dose Efficacy (Part B) in Participants With Duchenne Muscular Dystrophy Amenable to Exon 51-Skipping Treatment (MOMENTUM)
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT04004065 |
Recruitment Status :
Active, not recruiting
First Posted : July 1, 2019
Last Update Posted : December 1, 2023
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Sponsor:
Sarepta Therapeutics, Inc.
Information provided by (Responsible Party):
Sarepta Therapeutics, Inc.
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No Study Results Posted on ClinicalTrials.gov for this Study
Recruitment Status : | Active, not recruiting |
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Actual Primary Completion Date : | October 30, 2023 |
Estimated Study Completion Date : | January 31, 2029 |