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Clinical Trial Summary

Study to assess safety and tolerability of a single dose of study-drug administered to Cystic Fibrosis (CF) patients.


Clinical Trial Description

n/a


Study Design

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


Related Conditions & MeSH terms


NCT number NCT01347190
Study type Interventional
Source CSL Behring
Contact
Status Completed
Phase Phase 1
Start date April 2011
Completion date August 2011

See also
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