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Clinical Trial Summary

The study will be performed to obtain further efficacy and safety data in order to obtain a marketing authorization (pivotal study). In addition, health economic data are to be collected.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00836654
Study type Interventional
Source Neovii Biotech
Contact
Status Completed
Phase Phase 2/Phase 3
Start date September 2004
Completion date November 2006

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