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Virus Therapy
HIV Vaccine for Human Immunodeficiency Virus Infection
Phase 1
Waitlist Available
Led By Marina Caskey, MD
Research Sponsored by International AIDS Vaccine Initiative
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 18 months
Summary
This trial is testing a new HIV vaccine in healthy adults who do not have HIV. The vaccine works by teaching the immune system to recognize and fight HIV.
Eligible Conditions
- Human Immunodeficiency Virus (HIV) Infection
- HIV Suppression
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 18 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~18 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Safety - Grade 2 or greater unsolicited AEs
Safety - IP related SAEs
Safety - IP related unsolicited adverse events
+2 moreSecondary study objectives
Immunogenicity - Frequency Ab responses
Immunogenicity - Magnitude Ab responses
Trial Design
2Treatment groups
Experimental Treatment
Group I: Investigational Product, 300 µg/ PlaceboExperimental Treatment2 Interventions
300 µg IM, months 0, 2 and 6
Group II: Investigational Product, 30 µg/ PlaceboExperimental Treatment2 Interventions
30 µg IM, months 0, 2 and 6
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
BG505 SOSIP GT1.1 gp140 Vaccine, Adjuvanted
2020
Completed Phase 1
~50
Placebo
1995
Completed Phase 3
~2670
Find a Location
Logistics
Participation is compensated
You will be compensated for participating in this trial.
Who is running the clinical trial?
International AIDS Vaccine InitiativeLead Sponsor
51 Previous Clinical Trials
13,468 Total Patients Enrolled
George Washington UniversityOTHER
254 Previous Clinical Trials
466,547 Total Patients Enrolled
Rockefeller UniversityOTHER
160 Previous Clinical Trials
16,478 Total Patients Enrolled
GlaxoSmithKlineIndustry Sponsor
4,812 Previous Clinical Trials
8,382,200 Total Patients Enrolled
Amsterdam UMC, location VUmcOTHER
413 Previous Clinical Trials
216,691 Total Patients Enrolled
Marina Caskey, MDPrincipal InvestigatorRockefeller University
15 Previous Clinical Trials
695 Total Patients Enrolled
Godelieve de Bree, MD, PhDPrincipal InvestigatorAmsterdam UMC, location VUmc
1 Previous Clinical Trials
24 Total Patients Enrolled
David Joseph Diemert, MDPrincipal InvestigatorGeorge Washington University
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:Research Study Groups:
This trial has the following groups:- Group 1: Investigational Product, 300 µg/ Placebo
- Group 2: Investigational Product, 30 µg/ Placebo
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.