The purpose of this study is to look at whether an investigational drug can treat the breathing symptoms of RSV bronchiolitis in children 3 to 24 months of age.

Condition	Treatment or Intervention	Phase
Bronchiolitis		Phase II Phase III

Ages Eligible for Study:  3 Months   -   24 Months,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

• Hospitalized or in an urgent/emergent-care setting at least 24 hours for a first or second episode of RSV-induced bronchiolitis. Approximately twenty percent of patients will be allowed in the study with a stay of less than 24 hours but need to meet a minimum predefined Respiratory Severity Score as required by the study.

Exclusion Criteria:

• Asthma or other wheezing disorder. The Primary Investigator will evaluate whether there are other reasons why a child may not participate.

Toll Free Number      1-888-577-8839 

California
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Colorado
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Connecticut
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Florida
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Georgia
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Illinois
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Indiana
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Kentucky
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Louisiana
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Massachusetts
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Michigan
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Nebraska
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New Jersey
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New York
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North Carolina
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Ohio
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Pennsylvania
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Rhode Island
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Tennessee
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Texas
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Utah
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Washington
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West Virginia
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Wisconsin
      Call for Information, Marshfield,  Wisconsin,  54449,  United States; Recruiting
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Study ID Numbers:  0112BRS
Record last reviewed:  March 2005
Last Updated:  March 29, 2005
Record first received:  February 6, 2004
ClinicalTrials.gov Identifier:  NCT00076973
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-04-08