Trials / Completed
CompletedNCT00097591
A Comparison of Prasugrel (CS-747) and Clopidogrel in Acute Coronary Syndrome Subjects Who Are to Undergo Percutaneous Coronary Intervention
A Comparison of CS-747 and Clopidogrel in Acute Coronary Syndrome Subjects Who Are to Undergo Percutaneous Coronary Intervention
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 13,619 (actual)
- Sponsor
- Eli Lilly and Company · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The sponsors of this investigational drug are developing prasugrel (also known as CS-747) as a possible treatment for patients with acute coronary syndrome (heart attack or chest pain) who need, or are expected to need, a percutaneous coronary intervention (PCI; also called a balloon angioplasty). Prasugrel was compared with Clopidogrel to determine which drug is better at reducing deaths, future heart attacks, or stroke.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Prasugrel | Administered orally |
| DRUG | Clopidogrel | Administered orally |
Timeline
- Start date
- 2004-11-01
- Primary completion
- 2007-07-01
- Completion
- 2007-07-01
- First posted
- 2004-11-25
- Last updated
- 2010-09-16
- Results posted
- 2010-09-16
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00097591. Inclusion in this directory is not an endorsement.