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Clinical Trial Summary

This study aims to evaluate the safety, tolerability and effectiveness of BTA798 on

- shortening the length and reducing the symptoms of human rhinovirus infection (also known as the common cold),

- controlling asthma symptoms, and

- lowering the risk of asthma symptoms worsening in subjects with asthma.


Clinical Trial Description

Subjects with a previous diagnosis of asthma will be pre screened within 90 days prior to enrolment. If a subject develops symptoms of human rhinovirus (HRV) infection they will visit the site for assessment. Symptomatic subjects meeting all eligibility criteria will be invited to enroll. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01175226
Study type Interventional
Source Vaxart
Contact
Status Completed
Phase Phase 2
Start date August 2010
Completion date March 2012

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