Enrolling by invitationPhase 1NCT05983874
A Study to Evaluate the Safety and Immunogenicity of 2 Doses of 100µg BG505 SOSIP.664 gp140 Vaccine, Adjuvanted, Given to a Population of Adults Who Have Received 3 Doses of 300µg BG505 SOSIP.GT1.1 gp140 Vaccine, Adjuvanted
Studying Acquired immunodeficiency
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- International AIDS Vaccine Initiative
- Principal Investigator
- Godelieve de BreeAmsterdam UMC, location VUmc
- Intervention
- BG505 SOSIP.664 gp140 Vaccine, Adjuvanted (3M-052 AF plus alum) Dosage(biological)
- Enrollment
- 8 enrolled
- Eligibility
- 18-51 years · All sexes
- Timeline
- 2024 – 2025
Study locations (1)
- The Amsterdam University Medical Centers, Amsterdam, Netherlands
Collaborators
3M · Access to Advanced Health Institute (AAHI) · Polymun Scientific GmbH
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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