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- CheckyesterdayChange DetectedRevision updated from v3.5.0 to v3.5.2.SummaryDifference0.1%

- Check8 days agoNo Change Detected
- Check16 days agoNo Change Detected
- Check23 days agoChange DetectedAdded disease-related MeSH terms (Neuronal ceroid lipofuscinosis type 2, Juvenile NCL, Late-infantile NCL) and a Resources link to Genetic and Rare Diseases Information Center. These elements provide additional context and navigation without altering core trial details.SummaryDifference0.3%

- Check30 days agoChange DetectedRevision history updated: added v3.5.0 and removed v3.4.3.SummaryDifference0.1%

- Check44 days agoChange DetectedRevision updated from v3.4.2 to v3.4.3 across the site.SummaryDifference0.1%

- Check65 days agoChange DetectedRevision: v3.4.2 replaces v3.4.1, updating an internal label without affecting the study details or site navigation. To avoid being alerted by small changes, set an alert condition by clicking below.SummaryDifference0.1%

- Check73 days agoChange DetectedSite revision updated from v3.4.0 to v3.4.1.SummaryDifference0.1%

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