Recruiting
Phase 2

Visbiome

Sponsor:

University Health Network, Toronto

Code:

NCT02441231

Conditions

HIV-1 Infection

Eligibility Criteria

Sex: Male

Age: 19+

Healthy Volunteers: Not accepted

Interventions

Visbiome

Placebo

Study Details

Brief summary:

Modern antiretroviral therapy (ART) has transformed the clinical care and lived experience of HIV infection. However, increased rates of adverse health conditions that are related to immune activation, such as cardiovascular disease (CVD) and neurodegenerative disease in ART-treated individuals persist. An important cause of this inflammation is the gut CD4 T cell loss and the "leaking" or translocation of luminal gut bacteria and other microbes across the bowel wall and into the bloodstream.

The use of complementary and alternative therapies is very common among people living with HIV, with estimates ranging from 16-60%. However, their efficacy has generally not been well demonstrated. Probiotics are live microbes that may provide a health benefit to the host and the investigators believe that the simultaneous use of probiotics along with ART will improve gut CD4 T cell restoration and function and therefore reduce microbial translocation and immune activation.

A major challenge to HIV treatment is the suboptimal CD4 T cell count despite successful HIV suppression on ART in immunologic non-responders (INRs). These individuals are at increased risk of AIDS-related deaths and non-AIDS related comorbidities that may be associated with increased immune activation and microbial translocation from the gut mucosa. With limited treatment options, alternative therapies to reduce inflammation and restore gut immunology will be important. Probiotic Visbiome consists of a high potency blend of eight different probiotics. The precise mechanism of action of Visbiome is unknown,but preclinical studies have shown that Visbiome may modulate the immune response towards an immunoregualtory phenotype with increased the levels of IL-10 and reduced levels of proinflammatory cytokines (TNFα, IL1β and IL-8). Therefore,the investigators believe that the "beneficial" bacteria from Visbiome will accelerate the normalization of gut immune cells and function in HIV-infected INRs. It is hypothesized consumption of Visbiome for 48 weeks will help restore the immune system in INRs who have suboptimal immune reconstitution to currently available ART. Resolution of gut immune cells will mean that microbial translocation and immune activation will be normalized and will reduce the rates of HIV-associated comorbidities.

Conditions

HIV-1 Infection

Study ID

NCT02441231

Start date

Nov, 2015

Status verified date

Apr, 2018

Completion date

May, 2019

Anticipated

Primary completion date

May, 2019

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: Male

Age: 19+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Documented HIV-1 infection
  • Male adult (age >18 years)
  • Currently on ART (>2 years but <10 years)
  • Undetectable HIV-1 viral load <50 copies/ml for the past 2 years (1 viral blip below 500 copies/ml permitted in the past year)
  • Last CD4 count <350 cells/μl, and >70% over the past 2 years <350 cells/μl
  • Ability to provide informed consent

Exclusion Criteria:

  • Current alcohol or substance use judged by the Investigator to potentially interfere with subject study compliance
  • Taking pharmaceutical-grade probiotics
  • Any of the following abnormal laboratory results in screening:

  • Hemoglobin <85 g/L
  • Neutrophil count <750 cells/μl
  • Platelet count <50,000 cells/μL
  • AST or ALT >5X the upper limit of normal
  • Colitis
  • Liver fibrosis (decompensated cirrhosis), portal hypertension or clinical hepatitis
  • Other significant underlying disease (non-HIV-1) that might impinge upon disease progression or death

Study Design

Enrollment

36 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Probiotic Group

Visbiome probiotic group (900 billion bacteria daily; 2 sachets daily)

placebo comparator: Placebo Group

Placebo comparator group

Interventions

Visbiome

Visbiome probiotic

Placebo

Placebo

Primary outcome measure

  • Percent change in blood immune activation [ Time Frame: 48 weeks ]

Central Contacts and Locations

Locations

Maple Leaf Medical Clinic

Recruiting

Toronto, Ontario, Canada, M5G 1K2

Contacts

Principal Investigator:

Colin Kovacs, MD

Toronto General Hospital, UHN

Recruiting

Toronto, Ontario, Canada, M5G 2N2

Contacts

Principal Investigator:

Sharon Walmsley, MD

More Information

Sponsor

University Health Network, Toronto

Last update posted

Apr 18, 2018

Last verified

Apr, 2018

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University Health Network, Toronto on 2018-04-18.