Pharmacokinetics of Imrecoxib in Subjects With Hepatic Insufficiency
- Registration Number
- NCT02456688
- Lead Sponsor
- Jiangsu HengRui Medicine Co., Ltd.
- Brief Summary
This clinical research study will assess pharmacokinetics and the safety of Imrecoxib in patients with impaired hepatic function as compared to healthy volunteers.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
All subjects:
- Between the ages of 18 to 70 years, with BMI 18~ 29kg/m2.
- In good health as determined by past medical history, physical examination, vital signs, electrocardiogram, and laboratory test values(except for values related to hepatic insufficiency).
Hepatic impaired subjects:
- Hepatocirrhosis subjects verified by B-mode ultrasonography,CT ,MRI or Biopsy.
- A Child-Pugh Classification score clinically determined as Class B.
Exclusion Criteria
All subjects:
- History of hypersensitivity to Imrecoxib or its components.
Subjects diagnosed with tumor.
- History of or current clinically important systemic illnesses, including but not limited to cardiovascular, pulmonary, renal, hematological, gastrointestinal, endocrinological, immunological, dermatological, or psychiatric diseases.
- Have used any drugs or substances (including herbal supplements) known to inhibit or induce cytochrome P450 enzymes including cytochrome P450 3A4, cytochrome P450 2C8 and cytochrome P450 2C9 within 28 days prior to the first dose and throughout the study.
- Have taken other investigational drugs or participated in any clinical trial within 90 days prior to first dose of study drug in this study.
Hepatic impaired subjects:
- Subjects with hepatic failure,or severe complications caused by Hepatocirrhosis.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Healthy Volunteers Imrecoxib One dose of Imrecoxib followed by 5 days' pharmacokinetic sample collection. Patients with im paired hepatic function Imrecoxib One dose of Imrecoxib followed by 5 days' pharmacokinetic sample collection.
- Primary Outcome Measures
Name Time Method Area under the concentration time curve from 0 to infinity (AUC0-∞) after a single First 5 days Time to maximum observed plasma drug concentration (Tmax) after a single oral dose of Imrecoxib. First 5 days Maximum observed plasma drug concentration (Cmax) after a single oral dose of First 5 days
- Secondary Outcome Measures
Name Time Method Apparent terminal half-life (t½) after a single oral dose of Imrecoxib. First 5 days Apparent clearance (CL/F) after a single oral dose of Imrecoxib. First 5 days
Trial Locations
- Locations (1)
The frist affiliated hospital of Fourth Military Medical University
🇨🇳Xi'an, Shanxi, China