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Safety, Tolerability and Immunogenicity of INO-4800 for COVID19 in Healthy Volunteers

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Contents

clinicaltrials.gov/study/NCT05430958
Is a
‌
Clinical study
0

Clinical Study attributes

NCT Number
NCT054309580
Trial Recruitment Size
00
Trial Sponsor
Inovio Pharmaceuticals
Inovio Pharmaceuticals
0
Clinical Trial Start Date
2022
0
Primary Completion Date
2024
0
Study Completion Date
2024
0
Clinical Trial Study Type
Interventional0
Interventional Trial Purpose
Prevention0
Intervention Type
Drug0
Device0
Intervention Name
INO-91120
CELLECTRA® 20000
INO-48000
Interventional Trial Phase
Phase 10
Official Name
Phase 1 Open Label Study to Evaluate the Safety, Tolerability, and Immunogenicity of an Intradermal Booster Dose of INO-4800 Alone or in Combination With INO-9112 Followed by Electroporation, in Adults Who Completed a Primary Immunization Series Against SARS-CoV-2 With mRNA Vaccines0
Last Updated
November 17, 2022
0
Allocation Type
Non-Randomized0
Intervention Model
Parallel Assignment0
Masking Type
None (Open Label)0
Study summary

This is an open label, phase 1 clinical trial of an intra-dermal booster dose of INO-4800 alone or in combination with INO-9112 followed by electroporation (EP) among healthy adults at least 18 years of age, who previously completed their primary immunization series with mRNA vaccines against SARS-CoV-2 within 6-12 months prior to the booster dose.

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