Raw research findings for this medication. Mostly single studies, not curated or confirmed robust.
Lopinavir is an HIV protease inhibitor that blocks the viral enzyme HIV needs to cut its proteins into working parts. It is always combined with ritonavir (as Kaletra), which slows its breakdown, and taken with other HIV medicines; it remains in use mainly for children and in some second-line treatments.
Lopinavir is broken down by CYP3A4, held back by ritonavir, and taken into the liver by the transporter SLCO1B1. Studies have linked the SLCO1B1 variant rs11045819 to lower lopinavir levels, and looked at ABCB1, ABCC2 and CYP3A5 for levels and response. The findings come from a few studies, and there is no CPIC or DPWG guideline.
Every published finding on gene variants and Lopinavir. Upload your DNA file to see which of these rows apply to you.
PharmGKB weighs all studies of a variant and rates how strong the evidence is, from 1A (strongest) to 4.
SLCO1B1 rs4149056: Level 3. Metabolism/PK: HIV infectious disease. 7.
ABCC2 rs8187710: Level 3. Efficacy: HIV infectious disease. 2.
CYP3A4 CYP3A4*1, CYP3A4*22: Level 3. Metabolism/PK: HIV infectious disease. 2.
ABCC2 rs8187710: Level 3. Other. 1.
Studies of how quickly the body processes this medication.
Studies of how well it worked in people carrying a variant.
Study findings and evidence levels: PharmGKB (CC BY-SA 4.0). Guidelines: CPIC and DPWG, as bundled in PharmCAT. Most studies were done mainly in people of European ancestry.
More drugs from the same category
Agenerase (Protease Inhibitors)
Crixivan (Protease Inhibitors)
Not a prescribing recommendation. This page is educational information about pharmacogenomic research and clinical guidelines - it is not medical or dosing advice, and not a prediction of how any medication will work for you. Never start, stop, or change a medication or dose based on it; talk to your doctor or pharmacist, who can order clinical-grade testing if appropriate.
Content updated September 2026.
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