BCG Vaccination Effect on Latent Reservoir Size in Treated HIV-1 Infection: (BELIEVE)

University of Zurich (UZH)

Status and phase: Active, not recruiting; Phase 2

Conditions: HIV-1-infection

Treatments: Biological: BCG Vaccine AJVaccines

Study type: Interventional

Funder types: Other

Identifiers

NCT05004038

2021-01481

Details and patient eligibility

About

A phase IIA randomized double-blind placebo-controlled single-centre study of the effect of Bacillus Calmette-Guérin (BCG) vaccination on the HIV latent reservoir

Full description

Background and Rationale:

HIV infection affects around 40 million people globally and is incurable due to persistence of viral genetic material within the host genome as the latent reservoir. Patients within the Swiss HIV Cohort Study with latent tuberculosis were recently shown to have a reduced set point HIV viral load compared to tuberculosis (TB)-naïve individuals. The BCG vaccine has been shown to have wide-ranging immunostimulatory effects and can simulate latent tuberculosis infection.

Objective(s):

The purpose of this study is to characterise potential sustained and clinically relevant effects of the BCG vaccine on the size of the latent HIV-1 reservoir in individuals with stable treated HIV-1 infection with suppressed viremia.

The study seeks primarily to determine the effect of a single dose of the BCG vaccine on the size of the latent HIV-1 viral reservoir over a period of up to 6 months post-administration compared to the size at baseline.

Study design:

Monocentric, randomized, placebo-controlled, stepped-wedge study design with all patients receiving BCG either at baseline or after three months

Measurements and procedures:

Measurement of the HIV-1 latent reservoir using peripheral blood mononuclear cells at three monthly intervals beginning on Day 0.

Study Product / Intervention: Single intradermal application of BCG Vaccine AJVaccines powder for suspension for injection according to the manufacturers' instructions.

Control Intervention: Single intradermal application of 0.1ml of 0.9% saline placebo using an identical procedure.

Number of Participants with Rationale: The study involves 60 participants in total, divided equally between two groups, who will receive early or late administration of the BCG vaccine.

Study Duration: The estimated study duration is 15 months

Statistical Considerations:

In order to power the trial to detect a relevant reduction of the HIV-1 latent reservoir with 90% certainty with a power of 80% at a probability of type 1 error of 5%, we need to enrol 54 patients (based on a paired t-test power calculation assuming the effect size mentioned in Section 10 and the variance of log- total HIV-1 DNA observed by Bachmann et al1). Assuming a drop-out of 10% this implies that 60 patients will be enrolled.

Enrollment: 60 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Informed consent as documented by signature (see Informed Consent Form),
• Age ≥18 years,
• HIV-1 infection under continuous antiretroviral therapy for ≥1.5 years as requested in the Systems X Cohort,
• Current participation in the Swiss HIV Cohort Study and past participation in the Systems X Cohort.

Exclusion criteria

• History of virological failure or treatment interruption at any time, defined as HIV-1 viral load >200c/ml at two consecutive measurements at least 4 weeks apart,
• CD4 T-cell count <200/μl at any time or <350/μl during the past 1 year
• Presence of other relevant immunosuppression according to the investigator in addition to HIV (a daily steroid intake of ≥20mg is considered clinically relevant),
• History of or current clinical evidence of active tuberculosis,
• Previous positive tuberculin skin test or tuberculosis INF-gamma release assay (Quantiferon-Test) within the past 10 years,
• Previous BCG-vaccination within the past 10 years,
• Known allergy to BCG vaccine or any of its components,
• Documented current febrile illness at screening or in the past 7 days.
• Women who are pregnant or breast-feeding

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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60 participants in 2 patient groups

Early Group

Active Comparator group

Description:

We will conduct a randomized, double-blind trial using a stepped-wedge design and involving a total of 60 patients with stable treated HIV and suppressed viral load who will all receive the BCG vaccine during the course of the study. Patients will be divided into two groups of equal size (early and late groups regarding administration of the BCG verum). The trial will be placebo-controlled and double-blind. Patients in the early group will receive the BCG verum at the beginning of Treatment Phase 1, and then the placebo at the beginning of Treatment Phase 2.

Treatment:

Biological: BCG Vaccine AJVaccines

Late Group

Active Comparator group

Description:

Patients in the late group will receive placebo at the beginning of Treatment Phase 1 and then the BCG verum at the beginning of Treatment Phase 2.

Treatment:

Biological: BCG Vaccine AJVaccines