drugset / Trial / NCT04588428
Safety, Tolerability and Immunogenicity of INO-4700 for MERS-CoV in Healthy Volunteers
Phase 2
Completed
192 enrolled
Inovio Pharmaceuticals
Coalition for Epidemic Preparedness Innovations · collab
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | INO-4700 | Vaccine | 0.6 mg | Other |
| Subject | INO-4700 | Vaccine | 1 mg | Other |
| Subject | INO-4700 | Vaccine | 2 mg | Other |