Viewing Study NCT05430958


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Study NCT ID: NCT05430958
Status: WITHDRAWN
Last Update Posted: 2022-11-17
First Post: 2022-06-21
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Safety, Tolerability and Immunogenicity of INO-4800 for COVID19 in Healthy Volunteers
Sponsor: Inovio Pharmaceuticals
Organization:

Study Overview

Official Title: 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 Vaccines
Status: WITHDRAWN
Status Verified Date: 2022-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Study was withdrawn due to sponsor decision.
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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.
Detailed Description: None

Study Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: True
Is an Unapproved Device?: True
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: