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Study to Evaluate the Safety of a Bivalent Vaccine of New 6:2 Influenza Virus Reassortants in Healthy Adults

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00192127
First Posted: September 19, 2005
Last Update Posted: December 18, 2007
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
MedImmune LLC
September 12, 2005
September 19, 2005
December 18, 2007
August 2004
Not Provided
The primary endpoint of this study is fever (Day 0-7) defined as oral temperature ³101°F. [ Time Frame: Day 0-7 ]
Not Provided
Complete list of historical versions of study NCT00192127 on ClinicalTrials.gov Archive Site
Secondary endpoints of the study include other reported reactogenicity events and other adverse events that occur within seven days (Day 0-7) and fourteen days (Day 0-14) following vaccination [ Time Frame: Days 0-7; 0-14 ]
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Study to Evaluate the Safety of a Bivalent Vaccine of New 6:2 Influenza Virus Reassortants in Healthy Adults
A Prospective, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety of a Bivalent Vaccine of New 6:2 Influenza Virus Reassortants in Healthy Adults
This study is to assess the safety of a bivalent vaccine of two new 6:2 influenza virus reassortants in healthy adults prior to the release of the trivalent vaccine (FluMist) containing them.
The primary study objective is to assess the safety of a bivalent vaccine of two new 6:2 influenza virus reassortants in healthy adults prior to the release of the trivalent vaccine (FluMist) containing them. Safety will be demonstrated by similar fever rates (oral temperature ≥101°F Days 0-7) in vaccine and placebo recipients.
Interventional
Phase 3
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Prevention
Influenza
  • Biological: FluMist
    A single dose of either bivalent vaccine or placebo mist by intranasal spray on Study Day 0.
  • Other: Placebo
    A single dose of either bivalent vaccine or placebo mist by intranasal spray on Study Day 0
  • Active Comparator: 1
    FluMist
    Intervention: Biological: FluMist
  • Placebo Comparator: 2
    Placebo
    Intervention: Other: Placebo
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
300
February 2005
Not Provided

Inclusion Criteria:

  • 18-49 years of age (not yet reached their 50th birthday);
  • In good health;
  • Available by telephone;
  • Ability to understand and comply with the requirements of the protocol; and
  • Signed informed consent and HIPAA authorization.

Exclusion Criteria:

  • Any condition for which the inactivated influenza vaccine is indicated, including: chronic disorders of the pulmonary or cardiovascular systems, including asthma; chronic metabolic diseases (including diabetes mellitus) renal dysfunction, or hemoglobinopathies which required regular medical follow-up or hospitalization during the preceding year;
  • Acute febrile (>100.0°F oral) and/or respiratory illness, including cough or sore throat, within the 14 days prior to enrollment;
  • Hypersensitivity to egg or egg protein;
  • Hypersensitivity to gentamicin;
  • Any known immunosuppressive condition or immune deficiency disease, including HIV infection, or ongoing immunosuppressive therapy;
  • History of Guillan-Barré Syndrome;
  • Household contact who is immunocompromised (participant should also avoid close contact with immunocompromised individuals for at least 21 days);
  • Participation in another investigational trial within 30 days prior to enrollment or expected enrollment in another investigational trial during this study;
  • Chronic or regular use of antipyretic or analgesic medication on a daily or every other day basis; Notes: A daily dose of 81 mg of aspirin is not considered a contraindication to enrollment. Discontinuation of prophylactic use of antipyretic or analgesic medications at the time of enrollment and for fourteen days following vaccination is not considered a contraindication to enrollment.
  • Pregnancy or, in biologically capable women (e.g., menses within the last year) participant does not agree to use acceptable birth control measures as determined by the investigator continuously for three months after enrolling into the study (for those biologically capable, a urine pregnancy test must be performed on the day of vaccination with a negative result);
  • Breastfeeding or lactating women;
  • Administration of intranasal medications within two weeks prior to enrollment or expected receipt during this study;
  • Employees of the investigational site or their family member or any individuals involved with the conduct of the study; and
  • Any condition that in the opinion of the investigator, might interfere with the vaccine evaluation.
Sexes Eligible for Study: All
18 Years to 49 Years   (Adult)
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT00192127
MI-CP113
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Robert Walker, M.D., MedImmune Inc.
MedImmune LLC
Not Provided
Study Director: Robert Walker, MD Sponsor GmbH
MedImmune LLC
December 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP