A Post Marketing Surveillance to Evaluate the Safety and Efficacy of Brilinta

This study is currently recruiting participants. (see Contacts and Locations)
Verified June 2014 by AstraZeneca
Sponsor:
Information provided by (Responsible Party):
AstraZeneca
ClinicalTrials.gov Identifier:
NCT01611272
First received: May 25, 2012
Last updated: June 12, 2014
Last verified: June 2014
  Purpose

To identify the following items through the post marketing surveillance under routine clinical practice after marketing authorization of Brilinta Tablet: the occurrence of unrevealed Serious Adverse Events (SAEs), current status of occurrence of Adverse Events (AEs), the factors that may influence safety and efficacy of the drug.


Condition
Acute Coronary Syndromes

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: A Post Marketing Surveillance to Evaluate the Safety and Efficacy of Brilinta

Resource links provided by NLM:


Further study details as provided by AstraZeneca:

Primary Outcome Measures:
  • Number of Hemorrhage events [ Time Frame: up to 54 months ] [ Designated as safety issue: Yes ]
  • Number of other AEs [ Time Frame: up to 54 months ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • Number of Stroke events [ Time Frame: up to 54 months ] [ Designated as safety issue: No ]
    for efficacy

  • Number of Cardiovascular (CV) related deaths events [ Time Frame: up to 54 months ] [ Designated as safety issue: No ]
    for efficacy

  • Number of Myocardial Infarction events [ Time Frame: up to 54 months ] [ Designated as safety issue: No ]
    for efficacy


Estimated Enrollment: 3500
Study Start Date: April 2013
Estimated Study Completion Date: January 2017
Estimated Primary Completion Date: January 2017 (Final data collection date for primary outcome measure)
Groups/Cohorts
1
Unstable angina, Non ST-segment Elevation Myocardial Infarction or ST-segment elevation myocardial infarction including patients managed medically, and those who are managed with percutaneous coronary intervention or coronary artery by-pass grafting

Detailed Description:

A Post Marketing Surveillance to evaluate the safety and efficacy of Brilinta

  Eligibility

Ages Eligible for Study:   19 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population

Patients who take Brilinta according to the local approval condition

Criteria

Inclusion Criteria:

  • Patients with Acute Coronary Syndromes
  • Patients who are taking ticagrelor and ASA daily(75-150mg), or Patients who are taking ticagrelor only(In the case that the patients have contraindication with ASA. Contraindication should be recorded in accordance with local PI on CRFs)
  • Patients who have signed the Data release consent form prior to enrollment in this surveillance

Exclusion Criteria:

  • Patients with hypersensitivity to ingredients of this drug or with moderate or severe hepatic impairment or with medical history of intracranial hemorrhage
  • Patients with pathological hemorrhage at the time of administration
  • Patients being administrated strong CYP3A4 inhibitors
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01611272

Contacts
Contact: EunYoung Kim +82 2 2188 0905 ClinicalTrialTransparency@astrazeneca.com
Contact: Seongha Cho +82 2 2188 0985

Locations
Korea, Republic of
Research Site Not yet recruiting
Andong, Korea, Republic of
Research Site Recruiting
Andong, Korea, Republic of
Research Site Not yet recruiting
Andong-si, Korea, Republic of
Research Site Recruiting
Ansan-si, Korea, Republic of
Research Site Recruiting
Anyang-si, Korea, Republic of
Research Site Recruiting
Bucheon-si, Korea, Republic of
Research Site Recruiting
Busan, Korea, Republic of
Research Site Not yet recruiting
Busan, Korea, Republic of
Research Site Recruiting
Cheonan-si, Korea, Republic of
Research Site Recruiting
Chuncheon-si, Korea, Republic of
Research Site Recruiting
Daegu, Korea, Republic of
Research Site Not yet recruiting
Gimhae-si, Korea, Republic of
Research Site Recruiting
Goyang, Korea, Republic of
Research Site Not yet recruiting
Goyang-si, Korea, Republic of
Research Site Recruiting
Gumi-si,, Korea, Republic of
Research Site Recruiting
Iksan-si, Korea, Republic of
Research Site Recruiting
Incheon, Korea, Republic of
Research Site Recruiting
Jeonju-si, Korea, Republic of
Research Site Recruiting
Pusan, Korea, Republic of
Research Site Not yet recruiting
Pusan, Korea, Republic of
Research Site Not yet recruiting
Seoul, Korea, Republic of
Research Site Recruiting
Seoul, Korea, Republic of
Research Site Recruiting
Suncheon-si, Korea, Republic of
Research Site Recruiting
Suwon-si, Korea, Republic of
Research Site Not yet recruiting
Ulsan, Korea, Republic of
Sponsors and Collaborators
AstraZeneca
Investigators
Study Director: JooWon Lee AstraZeneca Korea
  More Information

No publications provided

Responsible Party: AstraZeneca
ClinicalTrials.gov Identifier: NCT01611272     History of Changes
Other Study ID Numbers: D5130L00019
Study First Received: May 25, 2012
Last Updated: June 12, 2014
Health Authority: Korea: Ministry of Food and Drug Safety

Keywords provided by AstraZeneca:
Unstable angina

Additional relevant MeSH terms:
Acute Coronary Syndrome
Myocardial Ischemia
Heart Diseases
Cardiovascular Diseases
Angina Pectoris
Vascular Diseases
Chest Pain
Pain
Signs and Symptoms

ClinicalTrials.gov processed this record on July 24, 2014