WHO ICTRP trial
A Randomised, Double-blind, Parallel Group, Phase 3, Efficacy and Safety Study…
EUCTR2006-000658-27-GB · EU Clinical Trials Register · Not Recruiting
Key facts
| Trial ID | EUCTR2006-000658-27-GB |
|---|---|
| Public title | A Randomised, Double-blind, Parallel Group, Phase 3, Efficacy and Safety Study of AZD6140 Compared with Clopidogrel for Prevention of Vascular Events in Patients with Non-ST or ST Elevation Acute Coronary Syndromes (ACS)[PLATO – Can PLATelet inhibition be Optimised to Prevent Vascular Events ?] - PLATO |
| Scientific title | A Randomised, Double-blind, Parallel Group, Phase 3, Efficacy and Safety Study of AZD6140 Compared with Clopidogrel for Prevention of Vascular Events in Patients with Non-ST or ST Elevation Acute Coronary Syndromes (ACS)[PLATO – Can PLATelet inhibition be Optimised to Prevent Vascular Events ?]… |
| Primary sponsor | AstraZeneca AB |
| Registry | EU Clinical Trials Register |
| Recruitment status | Not Recruiting |
| Study type | Interventional clinical trial of medicinal product |
| Phase | Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): no Therapeutic confirmatory - (Phase III): yes Therapeutic use (Phase IV): no |
| Countries | Portugal;Slovakia;Greece;Finland;Spain;Austria;Italy;United Kingdom;France;Hungary;Czech Republic;Belgium;Denmark;Germany;Netherlands;Sweden |
| Conditions | non-ST and ST elevation acute coronary syndromes (ACS) MedDRA version: 9 Level: HLT Classification code 10011085 |
| Interventions | Product Code: AZD6140 90 mg Pharmaceutical Form: Film-coated tablet INN or Proposed INN: ticagrelor CAS Number: 274693-27-5 Current Sponsor code: AZD6140 Concentration unit: mg milligram(s) Concentration type: equal Concentration number… |
| Registration date | Oct 5, 2006 |
| Target size | 18000 |
| Secondary IDs | D5130C05262 |
| Registry page | clinicaltrialsregister.eu |
At a glance
- Yes Results available
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About WHO ICTRP trial registrations
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: