Toll-like Receptor 9 Agonist Treatment in Chronic HIV-1 Infection

• Status: Completed
• Trial end date: 2017-06-25
• Target enrollment: 0
• Participant gender: All

Summary

Combination antiretroviral treatment (cART) effectively suppresses virus replication and partially restores immune functions. However, cART cannot cure HIV infection.

This study aim to investigate whether the antiviral immune response can be enhanced and/or viral transcription reactivated with MGN1703. MGN1703 is an agonist to toll-like receptor (TLR) 9. Activation of TLR9 has been shown to augment innate and adaptive immune effector functions, most notably enhanced NK cell and T cell functions.

Furthermore, TLR9 agonists have been shown in vitro to reactivate viral transcription in latently infected cells, potentially leading to enhanced recognition of infected cells by the immune effector cells.

• Phase: Phase 1/Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: University of Aarhus
• Treatments: CPG-oligonucleotide

Criteria

Inclusion Criteria:

• Documented HIV-1 infection

• Age >18 years

• CD4+ T-cell count >350/µL at screening

• On cART (for a minimum of 12 months)

• Able to give informed consent.

Exclusion Criteria:

• Pregnancy as determined by a positive urine beta-hCG (if female)

• Males or females who are unwilling or unable to use barrier contraception during sexual intercourse for the entire study period.

• Currently breast-feeding (if female)

• Viral load (HIV RNA) > 50 copies/mL

• Contraindication to receive MGN1703 as per current investigator brochure

• Presence of acute bacterial infection or undiagnosed febrile condition

• Concurrent chronic systemic immune therapy or immunosuppressant medication, including continuous systemic steroid treatment within the last 2 weeks prior to randomization

• Use of antibiotic therapy within the last 2 weeks prior to randomization

• Known HBV or HCV infection

• Any medical, psychiatric, social, or occupational condition or other responsibility that, in the judgment of the Principal Investigator (PI), would interfere with the evaluation of study objectives (such as severe alcohol abuse, severe drug abuse, dementia)

• Unable to follow protocol regimen