Long-term Effectiveness and Safety in Hepatitis-co-infected Patients

NCT01153269 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 33

Last updated 2011-12-19

Study results available
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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.

Conditions

  • Human Immunodeficiency Virus-Infection

Interventions

DRUG

Lopinavir/Ritonavir (Kaletra)

3 capsules 2xdaily or 2 tablets 2xdaily Kaletra

Sponsors & Collaborators

Principal Investigators

  • Stefan Simianer, MD · Abbott Germany, Medical Department

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2001-05-31
Primary Completion
2010-11-30
Completion
2010-11-30

Countries

  • Germany

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01153269 on ClinicalTrials.gov