Barely Significant
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Novel compounds for the treatment of Duchenne muscular dystrophy: emerging therapeutic agents.

Appl Clin Genet · 2011 · PMC3681176 · PMID 23776365

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Despite being very well tolerated, with no participants discontinuing the treatment due to adverse effects, the primary end point of change in the 6-minute walk test failed to reach statistical significance during the trial.

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