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Latest updates to the Pediatric CLN2 Disease Clinical Trial page
- Check3 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%

- Check10 days agoChange DetectedRevision history updated: added v3.5.0 and removed v3.4.3.SummaryDifference0.1%

- Check17 days agoNo Change Detected
- Check24 days agoChange DetectedRevision updated from v3.4.2 to v3.4.3 across the site.SummaryDifference0.1%

- Check45 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%

- Check53 days agoChange DetectedSite revision updated from v3.4.0 to v3.4.1.SummaryDifference0.1%

- Check75 days agoChange DetectedRevision tag updated to v3.3.4 (replacing v3.3.3). This is a minor metadata change and does not affect study content or user-facing functionality.SummaryDifference0.1%

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