drugset / Trial / NCT00455546

PLASMA Trial: A Dose-Response Study of A-002 In Subjects With Stable Coronary Artery Disease

NCT00455546 ↗

Phase 2 Completed 400 enrolled Anthera Pharmaceuticals
RandomizedParallel-groupDouble-blindPrevention

Summary

The study will be conducted at up to 80 centers worldwide 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 4 orally active doses of A-002. The duration of study drug therapy will be 8 weeks.

Timeline

Start
2007-04
Primary completion
—
Completion
2007-09

Drugs

EvaluationDrugModalityDoseRoute
Subject 1-H-indole-3-glyoxamide Unknown 50 mg Oral
Subject 1-H-indole-3-glyoxamide Unknown 100 mg Oral
Subject 1-H-indole-3-glyoxamide Unknown 250 mg Oral
Subject 1-H-indole-3-glyoxamide Unknown 500 mg Oral