TMC125-C223: TMC125 in HIV-1 Infected Subjects

Tibotec Pharmaceutical

Status and phase: Completed; Phase 2

Conditions: HIV Infection

Treatments: Drug: TMC125

Study type: Interventional

Funder types: Industry

Identifiers

NCT00081978

CR006736

Details and patient eligibility

About

The purpose of this study is to investigate the ability of TMC125, a Non-Nucleoside Reverse Transcriptase Inhibitor (NNRTI), to lower the amount of virus in your blood when administered twice daily for 48 weeks.

Full description

TMC125 will be given in addition to a combination of anti-HIV drugs that have been selected specifically for you by your doctor. There are three treatment groups in the study. One group will be given a dosage of TMC125, 400 mg twice daily. Another will be given 800 mg twice daily. The third group, a control arm, will not receive TMC125 (formulation TF035). The safety, tolerability and pharmacokinetics (determinations of the concentration of drug in your blood and its evolution over time) of TMC125 will also be evaluated in this study. Patients who have known resistance to NNRTIs and 3 or more protease inhibitor (PI) mutations may be eligible to participate. One-hundred-fifty (150) patients will be enrolled into this study. TMC125, 400mg twice daily for 48 weeks; TMC125, 800mg twice daily for 48 weeks.

Enrollment: 211 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• HIV-1 plasma viral load at screening >1000 copies/ml
• Documented genotypic evidence of resistance to currently available NNRTIs
• Previous NRTI experience for at least 3 months
• 3 primary PI mutations at screening

Exclusion criteria

• Chronic HBV and/or HCV with elevated liver function tests > 3x upper normal limits
• Any grade 3 or 4 toxicity according to the ACTG grading severity list (except for grade 3 glucose and asymptomatic triglyceride/cholesterol grade 3 or 4 elevation)
• Previous permanent discontinuation of any NNRTI due to cutaneous events.