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Active (not recruiting) Phase 2/3 NCT05502341

Study to Compare Bictegravir/Lenacapavir Versus Current Therapy in People With HIV-1 Who Are Successfully Treated With a Complicated Regimen

Phase 2/3 – combined trial
Conditions: HIV-1-infection

Sponsor: Gilead Sciences

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Overview
The goal of this clinical study is to learn more about the effects of switching to the study drugs, bictegravir (BIC) plus lenacapavir (LEN), versus current therapy (Phase 2) and BIC/LEN fixed-dose combination (FDC) versus current therapy (Phase 3) in people living with HIV (PWH).
Who can participate
Key Inclusion Criteria: * If plasma HIV-1 RNA measurements in the 6 months prior to screening are available, all levels must be \< 50 copies/mL. * At least one documented plasma HIV-1 RNA level measured between 6 and 12 months (± 2 months) prior to screening. This and any other HIV-1 RNA measurements documented in this period must be \< 50 copies/mL * Plasma HIV-1 RNA levels \< 50 copies/mL at screening. * Currently receiving a complex antiretroviral (ARV) regimen due to previous viral resistance, or intolerance, or contraindication to existing single-tablet regimens (STR), and on this regimen for at least 6 months prior to the screening visit. The criteria to define a complex regimen in this study are as follows: * A regimen containing a boosted protease inhibitor or a nonnucleos(t)ide reverse transcriptase inhibitor (NRTI) plus at least 1 other third agent (ie, an agent from a class other than NRTIs) (eg, bictegravir/emtricitabine/tenofovir alafenamide (coformulated; Biktarvy®)(BVY) + darunavir/cobicistat, BVY + etravirine), or * A regimen of ≥ 2 pills/day, or a regimen requiring dosing more than once daily, or * A regimen containing parenteral agent(s) (excluding a complete long-acting injectable regimen, such as intramuscular cabotegravir plus rilpivirine) as well as oral agents. * No documented or suspected resistance to bictegravir (BIC). * Estimated glomerular filtration rate ≥ 15 mL/min according to the Cockcroft-Gault formula for creatinine clearance (CLcr) who are not on renal replacement therapy. Key Exclusion Criteria: * Prior use of, or exposure to, lenacapavir (LEN) * Active tuberculosis infection * Chronic hepatitis B virus (HBV) infection Note: Other protocol defined Inclusion/Exclusion criteria may apply.
Locations 15
Argentina (1)
Hospital General de Agudos J.M Ramon Mejia
Buenos Aires
Australia (1)
St.Vincent's Hospital Sydney
Darlinghurst , New South Wales
Canada (1)
Chronic Viral Illness Service / McGill University Health Centre (MUHC)
Decarie Montreal
Dominican Republic (1)
Instituto Dominicano de Estudio Virologicos - IDEV
Santo Domingo
France (1)
CHU Nice-Hôpital l'Archet
Nice
Germany (1)
zibp Zentrum für Infektiologie Berlin Prenzlauer Berg GmbH
Berlin
Italy (1)
IRCCS Ospedale San Raffaele
Milan
Japan (1)
National Hospital Organization Nagoya Medical Center
Nagoya
Puerto Rico (1)
Hope Clinical Research
San Juan , PR
South Africa (1)
Desmond Tutu Health Foundation Clinical Trials Unit
Cape Town
South Korea (1)
Kyungpook National University Hospital
Daegu
Spain (1)
Hospital Clinic Provincial de Barcelona
Barcelona
Taiwan (1)
Kaohsiung Medical University Chung-Ho Memorial Hospital
Kaohsiung City
United Kingdom (1)
Department of HIV & Sexual Medicine
Birmingham
United States (1)
Be Well Medical Center
Berkeley , California
Technical details
Status
Active (not recruiting)
Phase
Phase 2/3
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
16.08.2022
Completion date
01.07.2028
Registry ID
NCT05502341
Source
anzctr
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Information is automatically extracted from ClinicalTrials.gov. Consult your doctor before taking action.