Study of VXCO-100, a SARS-CoV Candidate Vaccine in Healthy Adults in the United States
NCT05870839 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 121
Last updated 2024-12-10
Summary
The purpose of this study is to evaluate the safety and immunogenicity of ascending dose levels of VXCO-100 in healthy adults.
Conditions
- SARS-CoV
- SARS-CoV-2
Interventions
- BIOLOGICAL
-
VXCO-100
Sterile liquid for injection
Sponsors & Collaborators
-
Vaccine Company, Inc.
lead INDUSTRY
Principal Investigators
-
Justin Ortiz, MD, MS · University of Maryland
-
Nadine Rouphael, MD · Emory University
-
Angela Branche, MD · University of Rochester
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- PREVENTION
- Masking
- NONE
- Model
- SEQUENTIAL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2023-05-11
- Primary Completion
- 2024-04-10
- Completion
- 2024-04-10
- FDA Drug
- Yes
Countries
- United States
Study Locations
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