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Latest updates to the Study of ZX008 Oral Solution in Dravet Syndrome Clinical Trial page

  1. Check
    4 days ago
    Change Detected
    Summary
    Added a related topic 'Severe myoclonic epilepsy in infancy' and a 'Genetic and Rare Diseases Information Center' resources section.
    Difference
    0.1%
    Check dated 2026-04-02T05:48:21.000Z thumbnail image
  2. Check
    11 days ago
    Change Detected
    Summary
    Dravet syndrome is no longer listed on the page and the Genetics and Rare Diseases Information Center resource link has been removed, decreasing disease-specific context and external reference options for users.
    Difference
    0.1%
    Check dated 2026-03-26T02:44:58.000Z thumbnail image
  3. Check
    18 days ago
    Change Detected
    Summary
    Revision: v3.5.0 was added and Revision: v3.4.3 was removed from the page.
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    Check dated 2026-03-18T21:16:24.000Z thumbnail image
  4. Check
    25 days ago
    Change Detected
    Summary
    Updated the page revision from v3.4.2 to v3.4.3.
    Difference
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    Check dated 2026-03-11T17:52:10.000Z thumbnail image
  5. Check
    54 days ago
    Change Detected
    Summary
    Site-wide Revision: v3.4.2 was posted and the prior v3.4.1 funding/operating status notice was removed, with no changes to the study content on the NCT02926898 page. To avoid being alerted by small changes, set an alert condition by clicking below.
    Difference
    0.4%
    Check dated 2026-02-11T09:23:13.000Z thumbnail image
  6. Check
    61 days ago
    Change Detected
    Summary
    A new site-wide notice about a lapse in government funding was added, directing users to cc.nih.gov and opm.gov for updates. The revision tag was updated from v3.4.0 to v3.4.1.
    Difference
    0.4%
    Check dated 2026-02-04T05:36:37.000Z thumbnail image

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