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Investigating the Anti-Human Immunodeficiency Virus (HIV) & Anti-inflammatory Effect of Chloroquine

Primary Purpose

HIV Infections

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
chloroquine phosphate
Placebo
Sponsored by
University of Minnesota
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV Infections focused on measuring HIV, chloroquine, disease progression, inflammation, treatment naive

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: HIV-1 infected adults CD4 count > 250 cells/mm3 Not presently receiving HIV antiretroviral therapy (> 6 months or naΓ―ve) Viral load > 3000 RNA copies/mL (3.5 log) No planned HIV anti-retroviral therapy for 8 weeks Exclusion Criteria: Prior retinal eye disease CD4 < 250 cells/Β΅L Renal failure Active malignancy Corticosteroid therapy Age < 18 or > 65 years

Sites / Locations

  • Minnesota ACTU

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Chloroquine

Placebo

Arm Description

Chloroquine 205mg or 500mg orally once daily (Results pooled)

Placebo once daily for 8 weeks

Outcomes

Primary Outcome Measures

HIV Viral Load Change
HIV-1 viral load change between baseline and 8 weeks

Secondary Outcome Measures

Change in Immune Activation Assessed by Flow Cytometry Analysis From Baseline to 8 Weeks
The Change in the percentages of CD38+ HLA-DR+ CD8 and CD4 memory T cells from baseline to 8 weeks.

Full Information

First Posted
March 27, 2006
Last Updated
June 2, 2020
Sponsor
University of Minnesota
Collaborators
Minnesota Medical Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT00308620
Brief Title
Investigating the Anti-Human Immunodeficiency Virus (HIV) & Anti-inflammatory Effect of Chloroquine
Official Title
A Randomized, Pilot Study of the Anti-Viral and Anti-Inflammatory Effects of Chloroquine in Early HIV Infection
Study Type
Interventional

2. Study Status

Record Verification Date
June 2020
Overall Recruitment Status
Terminated
Why Stopped
Insufficient financial support; lack of efficacy for primary endpoint
Study Start Date
March 2006 (undefined)
Primary Completion Date
December 2008 (Actual)
Study Completion Date
June 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Minnesota
Collaborators
Minnesota Medical Foundation

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Summary: Chloroquine is a medication that in laboratory settings has significant anti-HIV effects in HIV infected T-cells. Chloroquine has been used safely for over 60 years for malaria treatment and prevention, and it also has significant anti-inflammatory effects. No formal study of chloroquine has been performed in people with HIV infection. Chloroquine is used worldwide and is quite inexpensive outside of the United States. If shown to be effective, chloroquine could be a very important tool worldwide in delaying HIV disease progression which would extend the time period without needing anti-retroviral therapy. In countries where anti-retroviral therapy is not available, this could be very helpful. This is an 8 week trial study requiring 3 study visits. Participants will be ask to take a once a day study medication (chloroquine or placebo) for 8 weeks and have three blood draws for CD4 counts, HIV viral loads, and other research tests. The visits are at study enrollment, 4 weeks, and 8 weeks.
Detailed Description
Summary: A phase I randomized, double-blind, placebo controlled trial to investigate the efficacy of chloroquine to decrease T-cell activation and decrease viral load in early HIV. Scientific Rationale: Chloroquine has in vivo direct anti-HIV effects and an anti-inflammatory effect. These properties may be beneficial in reducing viral burden and immune activation therefore delaying HIV disease progression. Sample Size: 25 Length of Study: 8 weeks, [enrollment + 2 follow up visits]. Intervention: Arm 1a: Chloroquine 250mg orally once daily for 8 weeks. Arm 1b: Chloroquine 500mg orally once daily for 8 weeks. Arm 2: Placebo once daily for 8 weeks. Measurements: Blood draws at weeks: 0, 4, and 8 weeks. CD4, viral load measurements will be communicated to the referring provider (with subject consent).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
HIV, chloroquine, disease progression, inflammation, treatment naive

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
13 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Chloroquine
Arm Type
Experimental
Arm Description
Chloroquine 205mg or 500mg orally once daily (Results pooled)
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo once daily for 8 weeks
Intervention Type
Drug
Intervention Name(s)
chloroquine phosphate
Other Intervention Name(s)
Aralen
Intervention Description
250mg or 500mg PO (by mouth) QDay
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo once daily for 8 weeks
Primary Outcome Measure Information:
Title
HIV Viral Load Change
Description
HIV-1 viral load change between baseline and 8 weeks
Time Frame
baseline and 8 weeks
Secondary Outcome Measure Information:
Title
Change in Immune Activation Assessed by Flow Cytometry Analysis From Baseline to 8 Weeks
Description
The Change in the percentages of CD38+ HLA-DR+ CD8 and CD4 memory T cells from baseline to 8 weeks.
Time Frame
8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: HIV-1 infected adults CD4 count > 250 cells/mm3 Not presently receiving HIV antiretroviral therapy (> 6 months or naΓ―ve) Viral load > 3000 RNA copies/mL (3.5 log) No planned HIV anti-retroviral therapy for 8 weeks Exclusion Criteria: Prior retinal eye disease CD4 < 250 cells/Β΅L Renal failure Active malignancy Corticosteroid therapy Age < 18 or > 65 years
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David R Boulware, MD, MPH
Organizational Affiliation
University of Minnesota
Official's Role
Principal Investigator
Facility Information:
Facility Name
Minnesota ACTU
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55455
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
20844049
Citation
Murray SM, Down CM, Boulware DR, Stauffer WM, Cavert WP, Schacker TW, Brenchley JM, Douek DC. Reduction of immune activation with chloroquine therapy during chronic HIV infection. J Virol. 2010 Nov;84(22):12082-6. doi: 10.1128/JVI.01466-10. Epub 2010 Sep 15.
Results Reference
result
Links:
URL
http://cvp.umn.edu
Description
University of Minnesota Clinical Virology Program

Learn more about this trial

Investigating the Anti-Human Immunodeficiency Virus (HIV) & Anti-inflammatory Effect of Chloroquine

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