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Study on the Usage, Dosing, Tolerability, and Effectiveness of Kaletra Tablet

Human Immunodeficiency Virus Clinical Trial

Official title:
Use of KALETRA® Tablets in Adult HIV-infected Patients: Data From the Multicenter Star/Stella Cohort

Clinical Trial Summary

The objective of this study is to observe and collect data on the usage, dosing, tolerability, and effectiveness of Kaletra (lopinavir/ritonavir) tablets in human immunodeficiency virus (HIV)-infected patients. In some patients, the study is to show the impact on tolerability of changing therapy to Kaletra tablets from other regimens.

Clinical Trial Description

This study was designed as a non-interventional observational study. Kaletra was prescribed in the usual manner in accordance with the terms of the local market authorization with regards to dose, population and indication as well as local guidelines. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01097655
Study type Observational
Source AbbVie
Contact
Status Completed
Phase N/A
Start date August 2006
Completion date January 2016
View Details
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