NCT07144293CompletedPhase 2
Improving Physical Ability and Cellular Senescence Elimination in HIV
Source: ClinicalTrials.gov · Last updated 15 Sept 2026
Brief summary (registry, in English)
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.
- Status (registry)
- Completed
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 82 (actual)
- First submitted
- 20 Aug 2025
- Start date
- 4 Dec 2025
- Primary completion date
- 26 Aug 2026
- Lead sponsor
- National Institute of Allergy and Infectious Diseases (NIAID)
- Diseases
- HIV
- NCT number
- NCT07144293
What you commit to
- Study type: Interventional · Phase 2
- Participants enrolled: 82
- From 4 Dec 2025 to the primary completion date, 26 Aug 2026
- 24 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Are on dialysis or have had a kidney transplant.
- Have a known history of pulmonary arterial hypertension or other respiratory disease requiring supplemental oxygen within 60 days before joining the study.
- Have uncontrolled diabetes with an HgbA1c level greater than 8% within 60 days before joining the study.
- Have had a significant illness within 60 days before joining the study.
Other illness
- Need to take medications that affect CYP3A4 or interact with dasatinib (e.g., certain HIV medications).
- Have an active cancer (except non-melanoma skin cancer).
- Have active liver disease with a Child Pugh score greater than 6, or other significant liver problems.
- Have had a heart attack, angina, stroke, or mini-stroke in the last 6 months.
Other
- Have used quercetin or dasatinib before.
- Have substance use that might interfere with study participation, as determined by the site investigator.
Who the study is looking for
- 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.
Age in the registry: 50 years to - · Sex: All · Does not accept healthy volunteers
Sites (24)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University of Colorado Hospital CRS (Site ID: 6101) Coordinator of this site? Confirm its status | Aurora | United States | Unknown status |
| Brigham and Women's Hospital Therapeutics Clinical Research Site (BWH TCRS) CRS (Site ID: 107) Coordinator of this site? Confirm its status | Boston | United States | Unknown status |
| Massachusetts General Hospital CRS (MGH CRS) (Site ID: 101) Coordinator of this site? Confirm its status | Boston | United States | Unknown status |
| Chapel Hill CRS (Site ID: 3201) Coordinator of this site? Confirm its status | Chapel Hill | United States | Unknown status |
| Cincinnati CRS (Site ID: 2401) Coordinator of this site? Confirm its status | Cincinnati | United States | Unknown status |
| Case CRS (Site ID# 2501) Coordinator of this site? Confirm its status | Cleveland | United States | Unknown status |
| Ohio State University CRS (Site ID: 2301) Coordinator of this site? Confirm its status | Columbus | United States | Unknown status |
| Greensboro CRS (Site ID: 3203) Coordinator of this site? Confirm its status | Greensboro | United States | Unknown status |
| Houston Advancing Research Team CRS (Site ID: 31473) Coordinator of this site? Confirm its status | Houston | United States | Unknown status |
| University of California, Los Angeles CARE Center CRS (Site ID: 601) Coordinator of this site? Confirm its status | Los Angeles | United States | Unknown status |
| Vanderbilt Therapeutics (VT) CRS (Site ID: 3652) Coordinator of this site? Confirm its status | Nashville | United States | Unknown status |
| New Jersey Medical School Clinical Research Center CRS [Site ID: 31786] Coordinator of this site? Confirm its status | Newark | United States | Unknown status |
| Weill Cornell Chelsea CRS (Site ID: 7804) Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| Weill Cornell Uptown CRS (Site ID: 7803) Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| Columbia Physicians & Surgeons (P&S) CRS (Site ID: 30329) Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| Penn Therapeutics, CRS (Site ID: 6201) Coordinator of this site? Confirm its status | Philadelphia | United States | Unknown status |
| University of Pittsburgh CRS (Site ID: 1001) Coordinator of this site? Confirm its status | Pittsburgh | United States | Unknown status |
| University of Rochester Adult HIV Therapeutic Strategies Network CRS (Site ID: 31787) Coordinator of this site? Confirm its status | Rochester | United States | Unknown status |
| UCSD Antiviral Research Center CRS (Site ID: 701) Coordinator of this site? Confirm its status | San Diego | United States | Unknown status |
| University of California, San Francisco HIV/AIDS CRS (Site ID: 801) Coordinator of this site? Confirm its status | San Francisco | United States | Unknown status |
| University of Washington Positive Research CRS (Site ID: 1401) Coordinator of this site? Confirm its status | Seattle | United States | Unknown status |
| Washington University Therapeutics (WT) CRS (Site ID: 2101) Coordinator of this site? Confirm its status | St Louis | United States | Unknown status |
| Harbor University of California Los Angeles Center CRS (Site ID: 603) Coordinator of this site? Confirm its status | Torrance | United States | Unknown status |
| Whitman-Walker Institute, Inc. CRS (Site ID: 31791) Coordinator of this site? Confirm its status | Washington D.C. | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.