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Clinical Trial Summary

To evaluate safety and tolerability of VM-1500A-LAI after its single and multiple intramuscular ascending dose to healthy volunteers


Clinical Trial Description

Primary Objective: To evaluate safety and tolerability of VM-1500A-LAI after its single and multiple intramuscular ascending dose to healthy volunteers. Secondary Objectives: To evaluate pharmacokinetic parameters of VM-1500A after its single and multiple intramuscular ascending dose administration to healthy volunteers. To evaluate safety and tolerability of ELPIDA®, administered in the run-in period ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03706911
Study type Interventional
Source Viriom
Contact
Status Completed
Phase Phase 1
Start date January 21, 2019
Completion date May 18, 2020

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