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Intranasal ALN-RSV01 Administered to Adult Volunteers Experimentally Inoculated With Respiratory Syncytial Virus

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Contents

clinicaltrials.gov/study/NCT00496821
Is a
‌
Clinical study
0

Clinical Study attributes

NCT Number
NCT004968210
Trial Recruitment Size
880
Trial Sponsor
Alnylam Pharmaceuticals
Alnylam Pharmaceuticals
0
Clinical Trial Start Date
2007
0
Study Completion Date
2007
0
Clinical Trial Study Type
Interventional0
Interventional Trial Purpose
Treatment0
Interventional Trial Phase
Phase 20
Participating Facility
Alnylam Pharmaceuticals
Alnylam Pharmaceuticals
0
Official Name
A Study to Investigate the Safety and Efficacy of Intranasal ALN-RSV01 Administered to Adult Volunteers Experimentally Inoculated With Respiratory Syncytial Virus0
Last Updated
November 30, 2007
0
Allocation Type
Randomized0
Intervention Model
Parallel Assignment0
Masking Type
Double0
Study summary

The purpose of this study is to determine the safety, tolerability and efficacy of intranasal ALN-RSV01 versus placebo, administered once daily for 5 days to a healthy male volunteers experimentally inoculated with RSV

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