Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
HIV -1 Infection
Type
Interventional
Phase
Phase 2
Design
Allocation: RandomizedIntervention Model: Factorial AssignmentIntervention Model Description: Participants will be randomized 1:1:1:1 in a blinded fashion to receive: Arm A: Placebo and Placebo Arm B: Lefitolimod and Placebo Arm C: Placebo and 3BNC117+10-1074 Arm D: Lefitolimod and 3BNC117+10-1074Masking: Double (Participant, Investigator)Masking Description: The participant and all study personnel who directly interact with study participants are blinded to study arm designation.Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 65 years
Gender
Both males and females

Description

Not Provided

Not Provided

Tracking Information

NCT #
NCT03837756
Collaborators
  • Aalborg University Hospital
  • Odense University Hospital
  • Rigshospitalet, Denmark
  • Hvidovre University Hospital
  • The Peter Doherty Institute for Infection and Immunity
  • University of Utah
  • Oslo University Hospital
Investigators
Principal Investigator: Ole S Søgaard, MD PhD Aarhus University Hospital