Safety and Efficacy of Kaletra in ARV Therapy Experienced Patients

PHASE4CompletedINTERVENTIONAL
Enrollment

207

Participants

Timeline

Start Date

November 30, 2003

Primary Completion Date

December 31, 2006

Study Completion Date

December 31, 2006

Conditions
Human Immunodeficiency Virus
Interventions
DRUG

lopinavir/ritonavir

lopinavir/ritonavir 400 mg/100 mg bid 48 weeks of treatment

Trial Locations (13)

10300

Site Ref # / Investigator 4077, Mexico City

31310

Site Ref # / Investigator 4073, Chihuahua City

72570

Site Ref # / Investigator 4053, Puebla City

97219

Site Ref # / Investigator 4075, Mérida

Unknown

Site Ref # / Investigator 4074, León

Site Ref # / Investigator 4056, Mexico City

Site Ref # / Investigator 4054, Morelia

Site Ref # / Investigator 4072, Tepic

Site Ref # / Investigator 4052, Oaxaca City

Site Ref # / Investigator 4055, Culiacán

01030

Site Ref # / Investigator 4049, Mexico City

01120

Site Ref # / Investigator 4050, Mexico City

09220

Site Ref # / Investigator 4051, Mexico City

All Listed Sponsors
lead

AbbVie (prior sponsor, Abbott)

INDUSTRY

NCT00648999 - Safety and Efficacy of Kaletra in ARV Therapy Experienced Patients | Biotech Hunter | Biotech Hunter