drugset / Trial / NCT04588428

Safety, Tolerability and Immunogenicity of INO-4700 for MERS-CoV in Healthy Volunteers

NCT04588428 ↗

RandomizedParallel-groupQuadruple-blindPrevention

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.

Timeline

Start
2021-06-21
Primary completion
2023-01-19
Completion
2023-01-19

Drugs

EvaluationDrugModalityDoseRoute
Subject INO-4700 Vaccine 0.6 mg Other
Subject INO-4700 Vaccine 1 mg Other
Subject INO-4700 Vaccine 2 mg Other