Safety of Lopinavir/Ritonavir (Kaletra) in HIV/HCV Co-infected Subjects vs Baseline Liver Biopsy Metavir Score

PHASE4CompletedINTERVENTIONAL
Enrollment

86

Participants

Timeline

Start Date

October 31, 2002

Primary Completion Date

January 31, 2008

Study Completion Date

January 31, 2008

Conditions
HIV Infection
Interventions
DRUG

Lopinavir/Ritonavir

400 mg/ 100 mg BID. Both arms use Kaletra 400/100 mg BID, plus NRTI chosen by the investigator

Trial Locations (11)

00960

Site Reference ID/Investigator# 4118, Bayamón

00961

Site Reference ID/Investigator# 4119, Bayamón

00795

Site Reference ID/Investigator# 6298, Juana Díaz

00771

Site Reference ID/Investigator# 6284, Las Piedras

00680

Site Reference ID/Investigator# 4101, Mayagüez

00731

Site Reference ID/Investigator# 4116, Playa de Ponce

Site Reference ID/Investigator# 4099, Ponce

00717-1563

Site Reference ID/Investigator# 4117, Ponce

00926

Site Reference ID/Investigator# 4086, Rio Piedras

00908

Site Reference ID/Investigator# 4080, San Juan

00909

Site Reference ID/Investigator# 4100, Santurce

All Listed Sponsors
lead

AbbVie (prior sponsor, Abbott)

INDUSTRY

NCT00234975 - Safety of Lopinavir/Ritonavir (Kaletra) in HIV/HCV Co-infected Subjects vs Baseline Liver Biopsy Metavir Score | Biotech Hunter | Biotech Hunter