Pharmacokinetic Properties of Single and Multiple-dose Pitavastatin Calcium Tablet in Healthy Chinese Volunteers

Status

Active, not recruiting

Phases

Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR-OO-13004294

Enrollment

Unknown

Registered

2013-07-02

Start date

2007-03-01

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

Pharmacokinetic Properties

Interventions

1:pitavastatin

Eligibility

Sex/Gender

All

Age

23 Years to 26 Years

Inclusion criteria

Inclusion criteria: Healthy male and female chinese volunteers aged from 18 to 27 and with a body mass index between 19–24 kg/m2 . a healthy status confirmed by medical history, physical examination, 12-lead ECG, and laboratory tests (hematology, blood biochemistry, hepatic function, urinalysis, hepatitis B surface antigen, tests for alcohol and other drugs of abuse) and nonsmoking status.

Exclusion criteria

Exclusion criteria: any allergic history or history of cardiac, pulmonary, renal, hepatic, gastrointestinal or hematologic abnormality or any other acute or chronic disease. exposure to any investigational medication within 30 days of the first dose of study medication, pregnant or nursing women, women of childbearing potential not using a highly effective method of birth control.

Design outcomes

Primary

Measure	Time frame
plasma drug concentration;	—

Countries

China

Contacts

Public ContactFeng Ping

West China Hospital, Sichuan University

pfyq@yahoo.com+86 023 89012224

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 5, 2026