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NotableLead sponsor: Merck Sharp & Dohme LLC to Merck Sharp & Dohme LLCEnrollment closed, study ongoing · Eligibility criteria expanded, about 12 words · Secondary endpoints: details revised at 24 of 38 entries · 1 moreShow 4 more changesShow less
Enrollment closed, study ongoing
Eligibility criteria expanded, about 12 words
Secondary endpoints: details revised at 24 of 38 entries
Site details revised at 41 of 41 sites
MinorSite details revised at 27 of 41 sitesv25
MinorTrial sites expanded: 36 → 41 locationsv24
MinorTrial sites reduced: 41 → 36 locationsv23
MinorSite details revised at 1 of 41 sitesv22
Show 20 earlier versionsHide 20 earlier versions
MinorSite details revised at 3 of 41 sitesv21
MinorStudy sites: 40 to 41v20
MinorStudy sites: 39 to 40v19
MinorStudy sites: 37 to 39v18
MinorEligibility criteria expanded, about 11 wordsSite details revised at 1 of 37 sitesv17Show 1 more changeShow less
NotableTrial status: Not Yet Recruiting to RecruitingStudy sites: 0 to 2 · Start date changed from estimate of Jun 6, 2025 to Jun 11, 2025v2Show 2 more changesShow less
Study sites: 0 to 2
Start date changed from estimate of Jun 6, 2025 to Jun 11, 2025
MinorStudy First Submitted
Stopped: an ongoing trial was terminated, suspended or withdrawn.
Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The purpose of this study is to demonstrate that V181 is safe and well tolerated, elicits an immune response, and reduces the frequency of virologically confirmed dengue (VCD) of any severity, due to any of the 4 dengue serotypes, regardless of dengue serostatus at baseline in children 2 to 17 years of age.