drugset / Trial / NCT00967187

Safety and Efficacy Study of MPC-4326 for Treatment of Patients With HIV-1 Infection.

NCT00967187 ↗

Phase 2 Completed 32 enrolled Myrexis Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

To evaluate the antiretroviral activity and safety of 200 mg BID and 300 mg BID doses of MPC-4326 administered as monotherapy for 14 days to HIV-1 positive patients. Patients with an initial treatment response will have the option to continue MPC-4326 in combination with an Optimized Backround Regimen for a maximum of 72 weeks.

Timeline

Start
2008-05
Primary completion
2009-11
Completion
2009-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Bevirimat Small molecule 200 mg —
Subject Bevirimat Small molecule 300 mg —