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Clinical Trial Summary

The purpose of this study is to compare different up-dosing schedules with Osiris.


Clinical Trial Description

n/a


Study Design

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


Related Conditions & MeSH terms


NCT number NCT01240954
Study type Interventional
Source ALK-Abelló A/S
Contact
Status Terminated
Phase Phase 2
Start date December 2010

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