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Clinical Trial Summary

A phase 2, prospective, randomized, controlled, open-label (dose-blinded), parallel group, international multi-center study. The study will consist of four treatment groups - one control group (SoC) and three I-040202 groups receiving SoC plus 0.133 mg/mL, 0.4 mg/mL or 1.0 mg/mL I-040202.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00533793
Study type Interventional
Source Kuros Biosurgery AG
Contact
Status Completed
Phase Phase 2
Start date April 2007
Completion date May 2011

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