drugset / Trial / NCT00525954

PLASMA 2 Trial: Examination of Once Daily (QD) Dosing of A-002 In Subjects With Stable Coronary Artery Disease

NCT00525954 ↗

Phase 2 Completed 120 enrolled Anthera Pharmaceuticals
RandomizedParallel-groupDouble-blindPrevention

Summary

The study will be conducted at up to 25 U.S. centers and will be a double-blind randomized parallel group placebo controlled study among subjects with stable coronary artery disease (CAD). Subjects will be randomized to receive either placebo tablets or one of 2 orally active doses of A-002. The duration of study drug therapy will be 8 weeks.

Timeline

Start
2007-09
Primary completion
—
Completion
2007-12

Drugs

EvaluationDrugModalityDoseRoute
Subject A-002 Unknown 250 mg Oral
Subject A-002 Unknown 500 mg Oral