A Comparison of Antiplatelet Therapies in Asian Subjects With Acute Coronary Syndrome
A Comparison of Platelet Inhibition Following Prasugrel or Clopidogrel Administration in Asian Acute Coronary Syndrome Subjects Who Are to Undergo Percutaneous Coronary Intervention
Sponsor: Daiichi Sankyo Co., Ltd.
Listed as NCT00830960, this PHASE3 trial focuses on Acute Coronary Syndrome and remains completed. Sponsored by Daiichi Sankyo Co., Ltd., it has been updated 7 times since 2009, reflecting limited change activity. This study contributes longitudinal data to the cardiovascular research landscape.
Status Flow
Change History
7 versions recorded-
Sep 2025 — Present [monthly]
Completed PHASE3
-
Sep 2024 — Sep 2025 [monthly]
Completed PHASE3
-
Jul 2024 — Sep 2024 [monthly]
Completed PHASE3
-
Jan 2021 — Jul 2024 [monthly]
Completed PHASE3
-
Jun 2018 — Jan 2021 [monthly]
Completed PHASE3
▶ Show 2 earlier versions
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Feb 2017 — Jun 2018 [monthly]
Completed PHASE3
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Jan 2017 — Feb 2017 [monthly]
Completed PHASE3
First recorded
Feb 2009
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Daiichi Sankyo Co., Ltd.
- Eli Lilly and Company
For direct contact, visit the study record on ClinicalTrials.gov .
Study Locations
Bangkok, Thailand , Beijing, China , Chiang Mai, Thailand , Daegu, South Korea , Guangzhou, China , Hangzhou, China , Kwangju, South Korea , Nanjing, China , Seongnam-si, South Korea , Seoul, South Korea and 8 more locations