Clinical trial
Trial to Assess Safety, Efficacy, Tolerability and Immunogenicity of Influenza…
NCT00192166 · MedImmune LLC, Industry · Completed
Key facts
| NCT number | NCT00192166 |
|---|---|
| Title | Trial to Assess Safety, Efficacy, Tolerability and Immunogenicity of Influenza Virus Vaccine, Liquid Formulation (CAIV-T), Administered Concomitantly With a Combination Live, Attenuated, Mumps, Measles, and Rubella Vaccine in Healthy Children Aged 11 - 24 Months |
| Official title | Trial to Assess Safety, Efficacy, Tolerability and Immunogenicity of Influenza Virus Vaccine, Administered Concomitantly With a Combination Live, Attenuated, Mumps, Measles, and Rubella Vaccine in Healthy Children Aged 11 - 24 Months |
| Lead sponsor | MedImmune LLC, Industry |
| Collaborators | Wyeth is now a wholly owned subsidiary of Pfizer Industry |
| Status | Completed |
| Phase | Phase 2 |
| Study type | Interventional |
| Conditions | Influenza |
| Intervention type | Biological |
| Interventions | CAIV-T |
| Enrollment | 1,200 |
| Start date | Oct 1, 2002 |
| Primary completion | Mar 1, 2003 |
| Completion | May 1, 2003 |
| First posted | Sep 19, 2005 |
| Last update posted | Dec 8, 2008 |
| Countries | Singapore |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: