German Measles Vaccine |
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Clinical Trial: A Measles, Mumps, and Rubella Investigational Vaccine Trial
This study is no longer recruiting patients.
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Purpose
The purpose of this study is to test the safety of a measles, mumps, and rubella study vaccine made from a new measles stock seed (a component of the vaccine made in 2003) with rHA (recombinant human albumin).
| Condition | Treatment or Intervention | Phase |
|---|---|---|
| Measles | Vaccine: Measles, Mumps, Rubella study vaccine | Phase II Phase III |
MedlinePlus related topics: Measles
Study Type: Interventional
Study Design: Prevention, Randomized, Double-Blind, Active Control, Parallel Assignment, Safety/Efficacy Study
Eligibility
Ages Eligible for Study: 12 Months - 18 Months, Genders Eligible for Study: Both
Accepts Healthy Volunteers
Criteria
Inclusion Criteria:
- Healthy children 12 to 18 months of age.
Exclusion Criteria:
- Previous receipt of measles, mumps, rubella and/or varicella vaccine.
- Prior infection or exposure to (within last 4 weeks) measles, mumps, rubella, varicella and/or zoster.
- Any medical condition that might interfere with the immune response to the given vaccines (including HIV infection and/or cancer) or has undergone immunosuppressive (weakens your body’s ability to fight infection) therapy.
- History of seizures (convulsions)
- Allergies to any component of the vaccine, including sorbitol, gelatin, or neomycin.
- A recent (within the last 3 days) illness resulting in a fever (underarm temperature greater than 99.5° F [37.5° C]).
More Information
Record last reviewed: April 2005
Last Updated: April 29, 2005
Record first received: April 26, 2005
ClinicalTrials.gov Identifier: NCT00109278
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-05-03
Source: ClinicalTrials.gov
Cache Date: May 4, 2005

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