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Clinical Trial Summary

Primary

- To evaluate the efficacy of Pulmonaron in the decrease of interleukin-4/interferon gamma after second period of treatment

Secondary

- To evaluate the efficacy of Pulmonarom in the prevention of upper respiratory tract infections symptoms through patient evaluation of fever or respiratory presence after second period of treatment

- To evaluate loss of working or study days after second period of treatment

- To evaluate the safety and tolerability of Pulmonarom in the population under study


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00599417
Study type Interventional
Source Sanofi
Contact
Status Completed
Phase Phase 4
Start date December 2007
Completion date September 2008

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