Protease inhibitors shine in triple combinations.
Author information unavailable
Abstract
Author information unavailable
Abstract
Ritonavir, a protease inhibitor, demonstrated strong antiviral activity when combined with AZT and ddC at dosage levels of 1200, 600 and 2.25 mg respectively. Six-month therapy resulted in a median CD4 count increase that was nearly double from baseline, and significant viral load reductions that were sustained throughout the study. Ritonavir was generally well tolerated. A study using AZT and 3TC with an experimental protease inhibitor, indinavir, also greatly reduced viral loads. The effects lasted throughout the six-month treatment period. A specific HIV protease gene that contributes to the emergence of resistance during treatment with ritonavir has also been identified.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Ritonavir, a protease inhibitor, demonstrated strong antiviral activity when combined with AZT and ddC at dosage levels of 1200, 600 and 2.25 mg respectively. Six-month therapy resulted in a median CD4 count increase that was nearly double from baseline, and significant viral load reductions that were sustained throughout the study. Ritonavir was generally well tolerated. A study using AZT and 3TC with an experimental protease inhibitor, indinavir, also greatly reduced viral loads. The effects lasted throughout the six-month treatment period. A specific HIV protease gene that contributes to the emergence of resistance during treatment with ritonavir has also been identified.
Key concepts: Indinavir, Ritonavir, Protease inhibitor (pharmacology), Protease, Viral load, Virology, Pharmacology, HIV-1 protease