At a glance
ClinicalIndex Comparison RecordN/ACompleted· 33 enrolled
Drug / intervention
Lopinavir/Ritonavir (Kaletra)drug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Long-term Effectiveness and Safety in Hepatitis-co-infected Patients
In Brief
An observational study evaluating Lopinavir/Ritonavir (Kaletra) for Human Immunodeficiency Virus-Infection. Completed, enrolled 33 participants across 8 sites.
Detailed Summary
The aim of the study is to observe the tolerability and effectiveness of Kaletra in Human Immunodeficiency Virus/Hepatitis-B Virus and Human Immunodeficiency Virus/Hepatitis-C Virus co-infected patients.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsHuman Immunodeficiency Virus-Infection
CountriesGermany
Collaborators--
Timeline
N/ACompletedFinished
200120022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartMay 2001
First PostedJun 2010
Primary CompletionNov 2010
TodayJul 2026
First PostedJun 30, 2010
Enrollment StartMay 1, 2001
Primary CompletionNov 1, 2010
TodayJul 2, 2026
Enrollment to primary: 9.5 yearsPosted 16.0 years ago
Interventions
Lopinavir/Ritonavir (Kaletra)drug
3 capsules 2xdaily or 2 tablets 2xdaily Kaletra