At a glance
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Study to Evaluate the Safety, Tolerability and Immunogenicity of INO-4700 for Middle East Respiratory Syndrome Coronavirus (MERS-CoV) in Healthy Volunteers
In Brief
A Phase 2 clinical trial evaluating INO-4700, Placebo, and 1 other intervention for Middle East Respiratory Syndrome Coronavirus (MERS-CoV). Completed, enrolled 192 participants across 6 sites in 3 countries.
Detailed Summary
The purpose of this Phase 2a, randomized, blinded, placebo-controlled, multi-center study is to evaluate the safety, tolerability and immunogenicity of INO-4700 administered by intradermal (ID) injection followed by electroporation (EP) using the CELLECTRA™ 2000 device in healthy adult volunteers for Middle East Respiratory Syndrome Coronavirus (MERS-CoV) infection. This study was divided into 2 parts: Part 1- dose finding stage and Part 2- dose expansion stage.
Study Details
Timeline
Interventions
INO-4700 was administered ID.
Sterile saline sodium citrate (SSC) buffer (SSC-0001) was administered ID.
EP using the CELLECTRA™ 2000 device was administered following ID drug administration
INO-4700
CELLECTRA™ 2000