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Probiotic Visbiome for Inflammation and Translocation in HIV II (PROOV IT II)

Primary Purpose

HIV-1 Infection

Status
Unknown status
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Visbiome
Placebo
Sponsored by
University Health Network, Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV-1 Infection

Eligibility Criteria

19 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

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

Sites / Locations

  • Maple Leaf Medical ClinicRecruiting
  • Toronto General Hospital, UHNRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Probiotic Group

Placebo Group

Arm Description

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

Placebo comparator group

Outcomes

Primary Outcome Measures

Percent change in blood immune activation
Percent change in blood immune activation (co-expression of CD38 and HLA-DR) on CD8 T cells at week 48 in participants randomized to probiotic Visbiome versus the placebo arm

Secondary Outcome Measures

Level of microbial translocation (including LSP and sCD14)
Plasma level of inflammation and coagulation (including IL-6, D-dimer and CRP)
Number and function of gut immune cells (including CD4 T cell subsets)
Intestinal permeability (Lac/Mac ratio)
Bacterial community diversity, determined by 16s rRNA gene sequencing of penile swabs
Bacterial community composition, determined by 16s rRNA gene sequencing of penile swabs
Gut HIV DNA levels
Canadian Diet History Questionnaire
Safety assessed by AE monitoring and participant questionnaire
Tolerability of Visbiome assessed by AE monitoring and participant questionnaire
Adherence to Visbiome assessed by participant questionnaire and sachet count

Full Information

First Posted
April 23, 2015
Last Updated
April 17, 2018
Sponsor
University Health Network, Toronto
Collaborators
CIHR Canadian HIV Trials Network
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1. Study Identification

Unique Protocol Identification Number
NCT02441231
Brief Title
Probiotic Visbiome for Inflammation and Translocation in HIV II
Acronym
PROOV IT II
Official Title
Probiotic Visbiome for Inflammation and Translocation in HIV II (PROOV IT II)
Study Type
Interventional

2. Study Status

Record Verification Date
April 2018
Overall Recruitment Status
Unknown status
Study Start Date
November 2015 (Actual)
Primary Completion Date
May 2019 (Anticipated)
Study Completion Date
May 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Health Network, Toronto
Collaborators
CIHR Canadian HIV Trials Network

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV-1 Infection

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
36 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Probiotic Group
Arm Type
Experimental
Arm Description
Visbiome probiotic group (900 billion bacteria daily; 2 sachets daily)
Arm Title
Placebo Group
Arm Type
Placebo Comparator
Arm Description
Placebo comparator group
Intervention Type
Drug
Intervention Name(s)
Visbiome
Intervention Description
Visbiome probiotic
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
Percent change in blood immune activation
Description
Percent change in blood immune activation (co-expression of CD38 and HLA-DR) on CD8 T cells at week 48 in participants randomized to probiotic Visbiome versus the placebo arm
Time Frame
48 weeks
Secondary Outcome Measure Information:
Title
Level of microbial translocation (including LSP and sCD14)
Time Frame
48 weeks
Title
Plasma level of inflammation and coagulation (including IL-6, D-dimer and CRP)
Time Frame
48 weeks
Title
Number and function of gut immune cells (including CD4 T cell subsets)
Time Frame
48 weeks
Title
Intestinal permeability (Lac/Mac ratio)
Time Frame
48 weeks
Title
Bacterial community diversity, determined by 16s rRNA gene sequencing of penile swabs
Time Frame
48 weeks
Title
Bacterial community composition, determined by 16s rRNA gene sequencing of penile swabs
Time Frame
48 weeks
Title
Gut HIV DNA levels
Time Frame
48 weeks
Title
Canadian Diet History Questionnaire
Time Frame
48 weeks
Title
Safety assessed by AE monitoring and participant questionnaire
Time Frame
48 weeks
Title
Tolerability of Visbiome assessed by AE monitoring and participant questionnaire
Time Frame
48 weeks
Title
Adherence to Visbiome assessed by participant questionnaire and sachet count
Time Frame
48 weeks
Other Pre-specified Outcome Measures:
Title
Metabolomic measurements: vitamin D levels, glucose measurements, insulin levels and lipid profiling
Time Frame
48 weeks
Title
Microbiome analysis by 16s rRNA bacterial DNA isolated from penile swabs
Time Frame
48 weeks

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rupert Kaul, MD
Phone
416-978-8607
Email
rupert.kaul@utoronto.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Rodney Rousseau
Phone
416-946-7054
Email
r.rousseau@mail.utoronto.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rupert Kaul, MD
Organizational Affiliation
University Health Network, Toronto
Official's Role
Principal Investigator
Facility Information:
Facility Name
Maple Leaf Medical Clinic
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 1K2
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Colin Kovacs, MD
Phone
416-465-3252
Email
ckovacs@mlmedical.com
First Name & Middle Initial & Last Name & Degree
Colin Kovacs, MD
Facility Name
Toronto General Hospital, UHN
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 2N2
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sharon Walmsley, MD
Phone
416-340-3871
Email
sharon.walmsley@uhn.ca
First Name & Middle Initial & Last Name & Degree
Sharon Walmsley, MD

12. IPD Sharing Statement

Citations:
PubMed Identifier
34693932
Citation
Rousseau RK, Walmsley SL, Lee T, Rosenes R, Reinhard RJ, Malazogu F, Benko E, Huibner S, Kovacs CM, Singer J, Kim CJ, Kaul R. Randomized, Blinded, Placebo-Controlled Trial of De Simone Formulation Probiotic During HIV-Associated Suboptimal CD4+ T Cell Recovery. J Acquir Immune Defic Syndr. 2022 Feb 1;89(2):199-207. doi: 10.1097/QAI.0000000000002840.
Results Reference
derived

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Probiotic Visbiome for Inflammation and Translocation in HIV II

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