Clinical Study to Evaluate Safety, Immunogenicity of Investigational Flu Vaccine Compared to an Approved Flu Vaccine in Children Previously Vaccinated in Trial V118_05 (NCT01964989)
| Status: | Not yet recruiting |
|---|---|
| Conditions: | Influenza |
| Therapuetic Areas: | Immunology / Infectious Diseases |
| Healthy: | No |
| Age Range: | Any |
| Updated: | 2/27/2016 |
| Start Date: | January 2016 |
| End Date: | April 2017 |
| Contact: | Novartis Drug Information Services |
| Phone: | 18002447668 |
Phase III, Randomized, Observer Blind, Multicenter Study to Evaluate the Safety and Immunogenicity of Repeated Exposure to Either the Same or Alternate Type of Vaccine, Adjuvanted or Non-adjuvanted Quadrivalent Subunit Influenza Virus Vaccine (aQIV or QIV), Administered to Subjects Previously Vaccinated in Trial V118_05 (NCT01964989)
Safety, Immunogenicity of an Adjuvanted Quadrivalent Subunit Influenza Virus Vaccine
Compared to Non-Adjuvanted Comparator Influenza Vaccine in Children Previously vaccinated in
Trial V118_05. Subjects will receive either the Same or Alternate Type of Vaccine.
Compared to Non-Adjuvanted Comparator Influenza Vaccine in Children Previously vaccinated in
Trial V118_05. Subjects will receive either the Same or Alternate Type of Vaccine.
Inclusion Criteria:
- Male or female subject who has completed their last visit in trial V118_05.
- Subject's parent/legal guardian has voluntarily given written informed consent after
the nature of the study has been explained according to local regulatory
requirements, prior to study enter
Exclusion Criteria:
- Individuals recently vaccinated against influenza
- Subjects with contraindications to receive influenza vaccines
- Please contact the site for additional eligibility criteria.
We found this trial at
19
sites
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