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Livalo Acute Myocardial Infarction Study

A Prospective Clinical Observation Study to Evaluate the Influence of Long Term Treatment of Pitavastatin on the Therapeutic Prognosis and Safety in Acute Myocardial Infarction

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00805714
Acronym
LAMIS
Enrollment
1128
Registered
2008-12-10
Start date
2007-04-30
Completion date
2011-03-31
Last updated
2012-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Myocardial Infarction

Keywords

Hydroxymethylglutaryl-CoA Reductase Inhibitors

Brief summary

Statins are usually used in AMI patients due to its strong anti-lipidemic effect, pleiotropic effect and tolerable safety profiles. Generally AMI patients are prescribed many drugs concomitantly; there are some risks due to the drug interaction. Especially, statins are reported to have many drug interactions, these might influence to therapeutic prognosis and safety in AMI patients. This study is conducted to administer the non-CYP3A4 metabolized statin, pitavastatin to AMI patients over 1 year, and the results will be compared with the other results from the KAMIR study which is expected to the large scale of AMI patients using statins be enrolled. Finally, from that comparison, we will investigate the influence of the statins metabolism by CYP3A4 to the therapeutic prognosis like death, major adverse cardiac events(MACE), and major ADR of statins like CK increase, myalgia.

Interventions

None listed

Sponsors

JW Pharmaceutical
Lead SponsorINDUSTRY

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* The patients who have taken pitavastatin since AMI

Exclusion criteria

* none

Design outcomes

Primary

MeasureTime frame
Death/MACE for 1 year after the registration1 year

Secondary

MeasureTime frame
Achievement of LDL cholesterol target level according to the NCEP ATP III guideline1 year
Abnormal change of lab value including CK etc1 year
Adverse event including myalgia1 year

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026