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Clinical Trial Summary

The purpose of this study is to assess the safety and tolerability of multiple doses of VB-201 administered for 4 weeks and its efficacy on biomarkers.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)


Related Conditions & MeSH terms


NCT number NCT01159730
Study type Interventional
Source Vascular Biogenics Ltd. operating as VBL Therapeutics
Contact
Status Completed
Phase Phase 2
Start date October 2010
Completion date October 2011

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