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Latest updates to the Embrace Watch Usability in Dravet Syndrome Clinical Trial page
- Check3 days agoNo Change Detected
- Check10 days agoChange DetectedFooter revision updated from v3.5.0 to v3.5.2.SummaryDifference0.1%

- Check17 days agoNo Change Detected
- Check24 days agoChange DetectedAdded a related topic Severe myoclonic epilepsy in infancy and a resources entry for the Genetic and Rare Diseases Information Center.SummaryDifference0.2%

- Check32 days agoChange DetectedThe study description no longer lists Dravet syndrome. The Genetic and Rare Diseases Information Center resource reference has been removed.SummaryDifference0.2%

- Check39 days agoChange DetectedSite revision updated from v3.4.3 to v3.5.0.SummaryDifference0.1%

- Check46 days agoChange DetectedThe page revision/version at the bottom was updated from v3.4.2 to v3.4.3.SummaryDifference0.1%

- Check67 days agoChange DetectedThe sub-study ZX008-1503-SS01 is terminated due to low enrollment and results are posted (Results First Posted 2023-11-13).SummaryDifference0.1%

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