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Clinical Trial Summary

This is a randomized and double-blinded within study group, placebo-controlled trial to evaluate the safety, tolerability and immunological profile of INO-4500 administered by intradermal (ID) injection followed by electroporation using the CELLECTRA® 2000 device in healthy adult volunteers.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03805984
Study type Interventional
Source Inovio Pharmaceuticals
Contact
Status Completed
Phase Phase 1
Start date May 9, 2019
Completion date October 21, 2020

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