At a glance
ClinicalIndex Comparison RecordPhase 3Completed· 875 enrolled
Drug / intervention
13vPnC +2 morebiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A PHASE 3, RANDOMIZED, OPEN-LABEL TRIAL TO EVALUATE THE SAFETY AND IMMUNOGENICITY OF A 20-VALENT PNEUMOCOCCAL CONJUGATE VACCINE IN ADULTS ≥65 YEARS OF AGE WITH PRIOR PNEUMOCOCCAL VACCINATION
In Brief
A Phase 3 clinical trial evaluating 13vPnC, PPSV23, and 1 other intervention for Pneumococcal Disease. Completed, enrolled 875 participants across 42 sites in 2 countries.
Detailed Summary
This Phase 3 will describe the safety and immunogenicity of a 20-valent pneumococcal conjugate vaccine formulation in adults 65 years of age or older with prior pneumococcal vaccination
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPneumococcal Disease
CountriesSweden, United States
Collaborators--
Timeline
Phase 3CompletedFinished
20192020202120222023202420252026
First PostedFeb 2019
Enrollment StartFeb 2019
Primary CompletionFeb 2020
TodayJul 2026
First PostedFeb 11, 2019
Enrollment StartFeb 12, 2019
Primary CompletionFeb 12, 2020
TodayJul 2, 2026
Enrollment to primary: 1 yearPosted 7.4 years ago
Interventions
13vPnCbiological
Pneumococcal conjugate vaccine
PPSV23biological
Pneumococcal polysaccharide vaccine
20vPnCbiological
Pneumococcal conjugate vaccine