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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
Awards & highlights

Study Summary

This trial is testing a new HIV vaccine to see if it is safe and causes an immune response.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~18 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 18 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Safety - Grade 2 or greater unsolicited AEs
Safety - IP related SAEs
Safety - IP related unsolicited adverse events
+2 more
Secondary outcome measures
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
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
48 Previous Clinical Trials
13,212 Total Patients Enrolled
George Washington UniversityOTHER
243 Previous Clinical Trials
453,726 Total Patients Enrolled
Rockefeller UniversityOTHER
158 Previous Clinical Trials
16,309 Total Patients Enrolled

Media Library

BG505 SOSIP GT1.1 gp140 Vaccine, Adjuvanted (Virus Therapy) Clinical Trial Eligibility Overview. Trial Name: NCT04224701 — Phase 1
Human Immunodeficiency Virus Infection Research Study Groups: Investigational Product, 300 µg/ Placebo, Investigational Product, 30 µg/ Placebo
Human Immunodeficiency Virus Infection Clinical Trial 2023: BG505 SOSIP GT1.1 gp140 Vaccine, Adjuvanted Highlights & Side Effects. Trial Name: NCT04224701 — Phase 1
BG505 SOSIP GT1.1 gp140 Vaccine, Adjuvanted (Virus Therapy) 2023 Treatment Timeline for Medical Study. Trial Name: NCT04224701 — Phase 1

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are there opportunities for volunteers to participate in this research endeavor?

"Clinicaltrials.gov has noted that while this trial, initially posted on August 1st 2020 and updated as recently as May 6th 2022, is no longer recruiting patients; there are 484 other trials actively looking for participants at the moment."

Answered by AI

To whom is this study open for participation?

"In order to be considered for this study, participants ought to have HIV and lie within the age range of 18-51. Currently, 48 applicants are being sought after by the clinical trial team."

Answered by AI

Does the age cutoff for this trial extend beyond eighty-five years of age?

"The age range for enrollment in this medical trial is 18 to 51 years old."

Answered by AI

Are there any known risks associated with the BG505 SOSIP GT1.1 gp140 Vaccine, Adjuvanted?

"The safety of the BG505 SOSIP GT1.1 gp140 Vaccine, Adjuvanted has been evaluated by our team at Power and given a score of 1 due to limited clinical data supporting its efficacy and safety in this Phase 1 trial."

Answered by AI
~10 spots leftby Apr 2025