drugset / Trial / NCT00455546
PLASMA Trial: A Dose-Response Study of A-002 In Subjects With Stable Coronary Artery Disease
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |