Clinical data | |
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AHFS/Drugs.com | International Drug Names |
MedlinePlus | a602015 |
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Routes of administration |
Oral |
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Pharmacokinetic data | |
Bioavailability | Unknown |
Protein binding | 98-99% |
Metabolism | Hepatic |
Biological half-life | 5 to 6 hours |
Excretion | Mostly fecal |
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CAS Number | |
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DrugBank | |
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ChEMBL | |
Chemical and physical data | |
Formula | C37H48N4O5 |
Molar mass | 628.810 g/mol |
3D model (Jmol) | |
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Lopinavir (ABT-378) is an antiretroviral of the protease inhibitor class. It is used against HIV infections as a fixed-dose combination with another protease inhibitor, ritonavir, under the trade names Kaletra (high-income countries) and Aluvia (low-income countries). It was first approved by the FDA on 15 September 2000.
Lopinavir is highly bound to plasma proteins (98–99%).
Reports are contradictory regarding lopinavir penetration into the cerebrospinal fluid (CSF). Anecdotal reports state that lopinavir cannot be detected in the CSF; however, a study of paired CSF-plasma samples from 26 patients receiving lopinavir/ritonavir found lopinavir CSF levels above the IC50 in 77% of samples.
Side effects, interactions, and contraindications have only been evaluated in the drug combination lopinavir/ritonavir.
A 2014 study indicates that lopinavir is effective against the human papilloma virus (HPV). The study used the equivalent of one tablet twice a day applied topically to the cervices of women with high-grade and low-grade precancerous conditions. After three months of treatment, 82.6% of the women who had high-grade disease had normal cervical conditions, confirmed by smears and biopsies.