HIV/AIDS Clinical Trials

Find HIV/AIDS Clinical Trials Near You

Improving Physical Ability and Cellular Senescence Elimination in HIV

Status: Active_not_recruiting
Location: See all (27) locations...
Intervention Type: Drug, Other
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This clinical trial is a Phase II study designed to test the safety and effectiveness of a combination of dasatinib and quercetin (D+Q) in improving physical function for people with HIV who are frail or prefrail. The study will involve 80 participants, all aged 50 or older, who have been living with HIV for at least 10 years determined to meet criteria for diagnosis of frail or prefrail and are currently on a stable antiretroviral therapy with viral suppression. Participants will be randomly assigned to one of two groups: one group will receive the D+Q treatment, and the other will receive a placebo. The treatment will be given in six cycles over 12 weeks, with participants taking the medication for two days followed by 12 days without treatment. After the 12-week treatment period, participants will be monitored for another 12 weeks to assess the long-term effects. The study aims to determine if D+Q can improve physical function and other health outcomes in this population. Randomization will be stratified by sex and age to ensure balanced groups.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 50
Healthy Volunteers: f
View:

• Must be an older person with confirmed diagnosis of HIV-1, defined as ≥ 50 years at study entry.

• Must have been diagnosed with HIV at least 10 years ago, as confirmed by medical records or self-report.

• Must be on a stable effective combination antiretroviral therapy (ART) regimen, with no changes in the regimen within 12 weeks before joining the study with 2 or more consecutive HIV-RNA levels \< 50 copies/mL within 48 weeks prior to study entry.

• Must meet one or more Fried Frailty Phenotype criteria w/in 60 days prior to entry.

• Must have eGFR \> 30 using CKD-EPI per 2021 calculation equation.

Locations
United States
Alabama
Alabama CRS (Site ID: 31788)
Birmingham
California
University of California, Los Angeles CARE Center CRS (Site ID: 601)
Los Angeles
UCSD Antiviral Research Center CRS (Site ID: 701)
San Diego
University of California, San Francisco HIV/AIDS CRS (Site ID: 801)
San Francisco
Harbor University of California Los Angeles Center CRS (Site ID: 603)
Torrance
Colorado
University of Colorado Hospital CRS (Site ID: 6101)
Aurora
Washington, D.c.
Whitman-Walker Institute, Inc. CRS (Site ID: 31791)
Washington D.c.
Georgia
The Ponce de Leon Center CRS (Site ID: 5802)
Atlanta
Illinois
Northwestern University CRS (Site ID: 2701)
Chicago
Massachusetts
Brigham and Women's Hospital Therapeutics Clinical Research Site (BWH TCRS) CRS (Site ID: 107)
Boston
Massachusetts General Hospital CRS (MGH CRS) (Site ID: 101)
Boston
Missouri
Washington University Therapeutics (WT) CRS (Site ID: 2101)
St Louis
North Carolina
Chapel Hill CRS (Site ID: 3201)
Chapel Hill
Greensboro CRS (Site ID: 3203)
Greensboro
New Jersey
New Jersey Medical School Clinical Research Center CRS (Site ID: 31786)
Newark
New York
Columbia Physicians & Surgeons (P&S) CRS (Site ID: 30329)
New York
Weill Cornell Chelsea CRS (Site ID: 7804)
New York
Weill Cornell Uptown CRS (Site ID: 7803)
New York
University of Rochester Adult HIV Therapeutic Strategies Network CRS (Site ID: 31787)
Rochester
Ohio
Cincinnati CRS (Site ID: 2401)
Cincinnati
Case CRS (Site ID: 2501)
Cleveland
Ohio State University CRS (Site ID: 2301)
Columbus
Pennsylvania
Penn Therapeutics CRS (Site ID: 6201)
Philadelphia
University of Pittsburgh CRS (Site ID: 1001)
Pittsburgh
Tennessee
Vanderbilt Therapeutics (VT) CRS (Site ID: 3652)
Nashville
Texas
Houston Advancing Research Team CRS (Site ID: 31473)
Houston
Washington
University of Washington Positive Research CRS (Site ID: 1401)
Seattle
Time Frame
Start Date: 2025-12-04
Completion Date: 2026-11-29
Participants
Target number of participants: 82
Treatments
Experimental: Arm A: D+Q
Placebo_comparator: Arm B: Placebo
Related Therapeutic Areas
Sponsors
Leads: National Institute of Allergy and Infectious Diseases (NIAID)
Collaborators: National Institute on Aging (NIA)

This content was sourced from clinicaltrials.gov