Phase I, Open Label Dose Ranging Safety Study of GLS-5300 in Healthy Volunteers

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ClinicalTrials.gov Identifier: NCT02670187

Recruitment Status : Completed

First Posted : February 1, 2016

Last Update Posted : January 9, 2019

View this study on Beta.ClinicalTrials.gov

Sponsor:

Collaborators:

Inovio Pharmaceuticals

Walter Reed Army Institute of Research (WRAIR)

Information provided by (Responsible Party):

GeneOne Life Science, Inc.

No Study Results Posted on ClinicalTrials.gov for this Study

About Study Results Reporting on ClinicalTrials.gov

Recruitment Status :	Completed
Actual Primary Completion Date :	May 2017
Actual Study Completion Date :	September 2017

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

Modjarrad K, Roberts CC, Mills KT, Castellano AR, Paolino K, Muthumani K, Reuschel EL, Robb ML, Racine T, Oh MD, Lamarre C, Zaidi FI, Boyer J, Kudchodkar SB, Jeong M, Darden JM, Park YK, Scott PT, Remigio C, Parikh AP, Wise MC, Patel A, Duperret EK, Kim KY, Choi H, White S, Bagarazzi M, May JM, Kane D, Lee H, Kobinger G, Michael NL, Weiner DB, Thomas SJ, Maslow JN. Safety and immunogenicity of an anti-Middle East respiratory syndrome coronavirus DNA vaccine: a phase 1, open-label, single-arm, dose-escalation trial. Lancet Infect Dis. 2019 Sep;19(9):1013-1022. doi: 10.1016/S1473-3099(19)30266-X. Epub 2019 Jul 24.

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