drugset / Trial / NCT00543725

TMC278-TiDP6-C215: A Clinical Trial in Treatment Naive HIV-subjects Patients Comparing TMC278 to Efavirenz in Combination With 2 Nucleoside/Nucleotide Reverse Transcriptase Inhibitors

NCT00543725 ↗

Phase 3 Completed 680 enrolled Tibotec Pharmaceuticals, Ireland
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this trial is to compare the effectiveness, safety and tolerability of TMC278 given at a dose of 25 mg once daily versus efavirenz (EFV) at a dose of 600 mg once daily, when combined with a background regimen containing 2 nucleoside/nucleotide reverse transcriptase inhibitors ( investigator choice of ABC/3TC, TDF/FTC or AZT/3TC) in HIV-1 infected patients who have not yet taken any anti-HIV drugs. The following evaluations will be done: antiviral activity, immunologic changes, and viral geno-/phenotype evolution, relationship of Pharmacokinetics (PK) and PK/Pharmacodynamics and Medical resource utilization and treatment adherence.

Timeline

Start
2008-06
Primary completion
2010-01
Completion
2012-02

Outcome

Met primary endpoint

registry analysis (non-inferiority or equivalence test); TMC278 vs Efavirenz; p <0.0001; Difference in proportion of response 3.7 (95% CI -1.6 to 9.0) NCT00543725 ↗

Drugs

EvaluationDrugModalityDoseRoute
Comparator Efavirenz Other / unclassified 600 mg Oral
Subject Rilpivirine Small molecule 25 mg Oral