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Completed Phase 1Phase 2 Interventional Results available

Safety and Efficacy of Sirolimus for HIV Reservoir Reduction in Individuals on Suppressive Antiretroviral Therapy (ART)

ClinicalTrials.gov ID: NCT02440789

Public ClinicalTrials.gov record NCT02440789. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 4, 2026, 12:41 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Safety and Efficacy of Sirolimus for HIV Reservoir Reduction in Individuals on Suppressive Antiretroviral Therapy

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study was to find out about the safety of sirolimus in individuals with HIV infection who were also being treated with ART. The investigators wanted to learn whether sirolimus decreases inflammation and immune activation in the body; whether sirolimus changes the level of HIV in the participants' blood; and how sirolimus interacts with ART in the blood. Sirolimus is approved by the Food and Drug Administration (FDA) to prevent organ rejection in patients aged 13 years and older receiving kidney transplants. Sirolimus had also been used for the prevention of complications after stem cell transplants and as a treatment for certain kinds of cancers in HIV-infected patients.

Study identification

NCT ID
NCT02440789
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Enrollment
32 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 20, 2015
Primary completion
Nov 1, 2017
Completion
Jan 31, 2018
Last update posted
Aug 2, 2021

2015 – 2018

United States locations

U.S. sites
10
U.S. states
9
U.S. cities
10
Facility City State ZIP Site status
801 University of California, San Francisco HIV/AIDS CRS San Francisco California 94110
Whitman Walker Health CRS (31791) Washington D.C. District of Columbia 20005
Univ. of Miami AIDS CRS (901) Miami Florida 33136
The Ponce de Leon Center CRS (5802) Atlanta Georgia 30308
Washington University CRS (2101) St Louis Missouri 63110
Weill Cornell Uptown CRS (7803) New York New York 10011
31787 University of Rochester Adult HIV Therapeutic Strategies Network CRS Rochester New York 14642
Univ. of Cincinnati CRS (2401) Cincinnati Ohio 45267
Houston AIDS Research Team CRS (31473) Houston Texas 77030
University of Washington AIDS CRS (1401) Seattle Washington 98104

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02440789, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 2, 2021 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02440789 live on ClinicalTrials.gov.

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