Condition: HIV-1-Infection · Sponsor: Gilead Sciences
The goal of this clinical study is to learn more about the safety and efficacy of switching to a once weekly tablet of islatravir/lenacapavir (ISL/LEN) regimen versus continuing standard of care treatment in people with human immunodeficiency virus (PWH) who are virologically suppressed (HIV-1 RNA levels \< 50 copies/mL) on a stable standard of care regimen for ≥ 6 months prior to screening. The standard of care includes 2 or 3 medicines, antiretroviral agents (ARVs). The primary objective of the study is to evaluate the efficacy of switching to oral weekly ISL/LEN tablet regimen versus continuing standard of care in virologically suppressed PWH at Week 48.
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
| University of Alabama at Birmingham(UAB) 1917 Research Clinic | Birmingham, Alabama, United States | — |
| Pueblo Family Physicians | Phoenix, Arizona, United States | — |
| Vv-Tmf-5366229 | Los Angeles, California, United States | — |
| Ruane Clinical Research Group | Los Angeles, California, United States | — |
| BIOS Clinical Research | Palm Springs, California, United States | — |
| Vivent Health | Denver, Colorado, United States | — |
| University of Colorado Clinical and Translational Research Center | Denver, Colorado, United States | — |
| Yale University; School of Medicine; AIDS Program | New Haven, Connecticut, United States | — |
| Georgetown University Medical Center | Washington D.C., District of Columbia, United States | — |
| Aids Healthcare Foundation - Northpoint | Fort Lauderdale, Florida, United States | — |
| Midway Immunology and Research Center | Ft. Pierce, Florida, United States | — |
| CAN Community Health | Miami Gardens, Florida, United States | — |
+ 88 more locations — full list on the registry record.
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