A safety study to compare, over a 7 day period, the fever rates following one dose of either Influenza Virus Vaccine or placebo administered outside the influenza season to healthy children and adolescents aged 6 to less than 18 years.

This was a prospective, randomized, double-blind, placebo-controlled, study. Subjects were randomized to receive either CAIV-T or Placebo. All subjects were healthy children and adolescents aged at least 6 years of age and less than 18 years of age at the time of enrollment.

Inclusion Criteria:

• who are aged 6 to less than 18 years at the time of enrolment
• who, if female and is of child bearing potential is using reliable method of hormonal and/or non-hormonal contraception (which includes cervical cap, diaphragm, condoms, with spermicide or IUD) during sexual intercourse throughout the entire study period; has provided a negative pregnancy test (with detection limit of less than or equal to 25mL/ml) no more than 24 hours prior to the study vaccine administration and agreed to avoid pregnancy during participation in the study.

N.B.lactating females are excluded from the study.

• who are in good health as determined by medical history, physical examination and clinical judgement
• whose parent(s)/legal guardian(s) have provided written informed consent after the nature of the study has been explained
• who, along with their parent(s)/legal guardian(s) will be available until completion of the study
• whose parent(s)/legal guardian(s), can be reached by study staff for the post vaccination contacts(telephone, clinic or home visit)

Exclusion Criteria:

• who along with their parent(s)/legal guardian(s) are perceived to be unavailable or difficult to contact for evaluation or study visits during the study period
• with any serious chronic disease (e.g. with signs of cardiac or renal failure or severe malnutrition) including progressive neurological disease
• with Down's syndrome or other known cytogenetic disorders
• with a known or suspected disease of the immune system or those receiving immunosuppressive therapy, including systemic corticosteroids; or cytotoxic agents
• who received any blood products, including immunoglobulin, in the period from six months prior to vaccination through to the conclusion of the study
• have an immunosuppressed or an immunocompromised individual living in the same household
• with a documented history of hypersensitivity to egg or egg protein or any other components of CAIV-T or placebo
• who have a history of Guillain-Barre Syndrome (GBS)
• for whom there is intent to administer any other investigational vaccine or agent from one month prior to enrollment through to the conclusion of the study
• who, in the two weeks prior to entry into the study, received a dose of influenza treatment (commercial or investigational)
• who received aspirin (acetylsalicylic acid) or aspirin-containing products in the two weeks prior to enrollment or for which use is anticipated during the study
• who, at anytime prior to study enrollment, received any influenza vaccine (commercial or investigational)
• with asthma requiring regular medical follow up or hospitalization during the preceding year
• with any medical conditions that in the opinion of the investigator might interfere with interpretation of the study results
• Note: Pregnancy in any person who has regular contact with the subjects is not a contraindication to enrollment or ongoing participation of the subject in the study.