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GLS-5310 Vaccine for COVID-19
Phase 1
Waitlist Available
Research Sponsored by GeneOne Life Science, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through 48 weeks post vaccination
Awards & highlights
No Placebo-Only Group
Summary
This trial tests the GLS-5310 DNA vaccine as a booster for people already vaccinated against COVID-19. It aims to enhance their immune response by introducing a small piece of viral DNA. The study will check if this new booster is safe and effective.
Eligible Conditions
- Coronavirus
- Healthy Subjects
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ through 48 weeks post vaccination
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through 48 weeks post vaccination
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Determine antibody responses after a single dose of vaccine
Incidence of adverse events
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
4Treatment groups
Experimental Treatment
Group I: GLS-5310 ID + GeneDerm 80 kPa, 30 secondsExperimental Treatment1 Intervention
GLS-5310 ID + GeneDerm administered at Visit 1
Group II: GLS-5310 ID + GeneDerm 65 kPa, 30 seconds + GLS-5310 INExperimental Treatment1 Intervention
GLS-5310 ID + GeneDerm + GLS-5310 IN administered at Visit 1
Group III: GLS-5310 ID + GeneDerm 65 kPa, 30 secondsExperimental Treatment1 Intervention
GLS-5310 ID + GeneDerm administered at Visit 1
Group IV: GLS-5310 ID + GeneDerm 65 kPa, 15 secondsExperimental Treatment1 Intervention
GLS-5310 ID + GeneDerm administered at Visit 1
Find a Location
Logistics
Participation is compensated
You will be compensated for participating in this trial.
Who is running the clinical trial?
GeneOne Life Science, Inc.Lead Sponsor
15 Previous Clinical Trials
1,371 Total Patients Enrolled