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Safety of intranasal palivizumab in healthy adult volunteers

Conditions
RSV
Registration Number
NL-OMON23479
Lead Sponsor
ouis Bontl.bont@umcutrecht.nl
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Other
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Adult men and women between the ages of 18 and 50 in good health based on relevant medical history

Exclusion Criteria

Adults with nasal cold or obstructions in the nasal cavity; history of respiratory symptoms or serious infectious disease within 4 weeks prior to drug administration; immunocomprimised; nasal surgery prior to or during trial

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Self-reported according to FDA scorecard and SAEs.
Secondary Outcome Measures
NameTimeMethod
Symptoms observed 10 minutes after first adminstration; viral diagnostics
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