Inhibiting the Anti-apoptotic Factor, BCL-2, at the Time of ART Initiation to Promote Apoptosis of HIV-infected Cells and Restrict the Seeding of the HIV Reservoir (The INITIATE Study)

ConditionHIV-1
Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18-70
SponsorThomas Aagaard Rasmussen

About this trial

Combination therapy with antiretroviral medication (ART) has proven effective in keeping HIV suppressed and restoring the immune system, but it cannot cure the infection. Therefore, lifelong treatment is necessary. The reason for this is a reservoir of inactive virus that remains hidden in long-lived cells and cannot be eliminated by either HIV treatment or the immune system. This reservoir is the primary barrier to a cure for HIV and must be minimized or eliminated in order to make it possible to discontinue lifelong ART treatment.

Several studies have been conducted with the aim of reducing the reservoir of inactive virus. The drugs used have been able to activate the virus in resting infected cells, thereby making the virus visible to the immune system. Unfortunately, this type of experimental treatment has not been sufficient to reduce the reservoir of inactive HIV in long-lived cells, possibly because these cells do not undergo cell death to a sufficient degree due to specific alterations in the mechanisms of cell death signaling.

The drug venetoclax (Venclyxto) is an inhibitor of BCL-2 (B Cell Lymphoma-2), a key factor involved in the regulation of programmed cell death. Studies have shown increased BCL-2 activity in long-lived cells infected with HIV. In laboratory experiments, we have demonstrated that treating cells with venetoclax while simultaneously activating HIV can lead to the elimination of HIV-infected cells. In experiments with HIV-infected humanized mice receiving ART, we further found that treatment with venetoclax delayed viral rebound after interruption of ART compared with mice that were not treated with venetoclax.

The purpose of this study is to investigate whether treatment with venetoclax in people with HIV who are initiating HIV therapy can promote the death of latently infected cells and thereby lead to a reduction in the latent HIV reservoir. The study will examine the safety and the effect of venetoclax.

Eligibility criteria

Qualifiers

Documented HIV-1 infection

Age 18-70 years (both included) at screening

CD4+ T cell count >300/µL at screening

ART naïve at screening

Disqualifiers

An individual who meets any of the following criteria will be excluded from participation in this study.

Current or previous use of a BCL-2 antagonist or other pro-apoptotic agent used as cancer therapy

Evidence of or strong suspicion that HIV infection was acquired during active PrEP use

Any concomitant disease where venetoclax treatment is indicated

Trial design

Treatments tested in this trial

  • Venetoclax

Treatment groups

38 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Thomas Aagaard Rasmussen

Lead sponsor

University of Aarhus

Sponsor institution

Germans Trias i Pujol Hospital

Collaborator

Walter and Eliza Hall Institute of Medical Research

Collaborator

The Alfred

Collaborator

Aarhus University Hospital

Collaborator