Not Signed In -
Vaccine |
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Clinical Trial: A Study of An Approved Vaccine at Mumps Expiry Potency in Healthy Children 12 to 18 Months of Age
This study is no longer recruiting patients.
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Purpose
The purpose of this study is to determine the mumps virus strength at the end of shelf-life (expiration date) of an approved vaccine.
| Condition | Treatment or Intervention | Phase |
|---|---|---|
| Measles Mumps Rubella Varicella | Vaccine: Investigational Vaccine | Phase IV |
MedlinePlus related topics: Chickenpox; Measles; Mumps; Rubella
Study Type: Interventional
Study Design: Prevention, Randomized, Double-Blind, Dose Comparison
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:
- History or prior exposure to measles, mumps, rubella or varicella
- History of anaphylactoid reactions or hypersensitivity to any component of the vaccine, including gelatin and neomycin
More Information
Study ID Numbers: 2004_073
Record last reviewed: September 2004
Last Updated: October 13, 2004
Record first received: September 22, 2004
ClinicalTrials.gov Identifier: NCT00092391
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-04-08
Record last reviewed: September 2004
Last Updated: October 13, 2004
Record first received: September 22, 2004
ClinicalTrials.gov Identifier: NCT00092391
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 9, 2005
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