PK/PD Study of Vicagrel and Clopidogrel in Healthy Subjects With Different CYP2C19 Metabolizers

Acute Coronary Syndrome Clinical Trial

Official title:

A Phase 1, Open-label, Randomized, Multiple-dose, Crossover Pharmacokinetic/Pharmacodynamic Study of Vicagrel and Clopidogrel in Healthy Subjects With Different CYP2C19 Phenotypes

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05162053
• Other study ID #: VCP1-?-06
• Status: Completed
• Phase: Phase 1
• Start date: December 9, 2021
• Est. completion date: November 3, 2022

Study information

• Verified date: November 2023
• Source: Jiangsu vcare pharmaceutical technology co., LTD
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This clinical study will adopt an open-label, randomized, multiple-dose, two-crossover design to explore the pharmacokinetic and pharmacodynamic profiles of Vicagrel Capsules and Clopidogrel Tablets in Healthy Subjects with Different CYP2C19 Metabolizers

Recruitment information / eligibility

• Status: Completed
• Enrollment: 128
• Est. completion date: November 3, 2022
• Est. primary completion date: November 3, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Able and willing to give written informed consent before study, and fully understand the study content, process and possible adverse reactions;

2. Able to complete the study in compliance with the protocol;

3. Subject (including partner) is willing to voluntarily take effective contraceptive measures from screening through 90 days after the last dose of study drug (see Appendix 5 for details);

4. Male and female subjects between the ages of 18 and 65 years, inclusive;

5. At least 50 kg for male subjects, 45 kg for female subjects, with a Body Mass Index (BMI= Weight/Height2) between 18-32 kg/m2, inclusive;

6. With normal or clinically insignificant abnormal results of physical examination and vital signs test;

7. Subjects will be assigned into the group according to the CYP2C19 genotype: the first group of ultra-rapid metabolizers (CYP2C19*17/*17); the second group of rapid metabolizers (CYP2C19*1/*17); the third group of normal metabolizers (CYP2C19*1/*1); the fourth group of intermediate metabolizers (CYP2C19*1/*2, *1/*3, *2/*17, *3/*17); and the fifth group of poor metabolizers (CYP2C19*2/*2, *2/*3, *3/*3).?

Exclusion Criteria:

1. More than 5 cigarettes per day on average within 3 months before the study;

2. History of sensitivity to drugs similar to the study drug or have high sensitivity to clopidogrel, allergic constitution (e.g. allergy to various drugs and foods);

3. History of drug abuse, drug use, alcohol abuse (14 units of alcohol per week: 1 units = 285 mL beer, 25 mL spirit or 100 mL wines);

4. Donation or loss of a significant volume of blood (> 450 mL) within 56 days prior to screening;

5. Intake of any prescription drugs, over-the-counter drugs, vitamin or herbal medicine within 14 days prior to receiving study drug;

6. Consumption of any special diet (such as grapefruit, pitaya, mango, pomelo, etc.) or subjects have engaged strenuous exercise or any other factors affecting drug absorption, distribution, metabolism and excretion within 14 days prior to receiving study drug;

7. Intake of any drug which Have taken strong inhibitors and/or inducers of liver metabolic enzymes (CYP1A2, 2A6, 2C8, 2C19, 3A4 and 3A5) within 28 days before the first medication, and strong inhibitors of liver metabolic enzymes such as: ciprofloxacin, clopidogrel, Itraconazole, ketoconazole, ritonavir, troleandomycin, etc., strong inducers of liver metabolism enzymes such as: rifampicin, carbamazepine, phenytoin sodium, St. John's wort, etc.(For details see Appendix 6);

8. Recent major changes in diet or exercise habits;

9. Use of an investigational drug or product, or participation in a drug research study within 30 days (or 5 half-lives) prior to receiving study drug;

10. History of difficulties in swallowing, or any gastrointestinal disease which could affect the drug absorption;

11. Suffering from any diseases that may increase the risk of bleeding, such as hemorrhoids, acute gastritis, stomach and duodenal ulcers, Thrombocytopenic Purpura and hemophilia, etc;

12. Family history of coagulation or bleeding disorders (e.g., hemophilia)/symptoms (e.g., vomiting blood, black stools, severe or recurrent nosebleeds, coughing up blood, significant hematuria, or intracranial hemorrhage) or suspected vascular malformations, such as aneurysms or early onset strokes, in the individual or in their immediate family;

13. A clinically significant 12-lead ECG abnormality;

14. Positive test results of blood pregnancy or subject is lactating for female subjects;

15. Any clinically significant abnormalities/findings in laboratory tests, or any clinically significant disease including but not limited to gastrointestinal, renal, hepatic, neurological system, blood, endocrine, tumor, lung, immune, mental, or cardiovascular and cerebrovascular diseases;

16. Positive test results for viral hepatitis (including hepatitis B and C), HIV antibody or syphilis antibody;

17. Acute illness or concomitant medication from screening to the first dosing of study medication;

18. Consumption of chocolate or any food or beverages containing caffeine or (rich containing) xanthine within 48 h prior to receiving the first dosing of study medication;

19. Consumption of any product containing alcohol within 24 h prior to receiving the first dosing of study medication, or positive results from a screen for alcohol;

20. Positive results from a screen for urine drug test (Morphine, marijuana);

21. Subjects were vaccinated within 4 weeks prior to screening, or planned to be vaccinated during the trial;

22. Any condition which in the opinion of Investigator is not suitable for subjects to participate in the study (For ultra-rapid metabolizers and rapid metabolizers, investigators may consider at their discretion).

Related Conditions & MeSH terms

• Acute Coronary Syndrome

Intervention

Drug:
• vicagrel Capsules
Oral administration for 7 days under fasting
• Clopidogrel Tablets
Oral administration for 7 days under fasting

Locations

Country	Name	City	State
China	Phase I Clinical Research Center of The First Hospital of Jilin University	Changchun	Jilin
United States	Altasciences, Kansas City	Kansas City	Missouri
United States	Altasciences Clinical, Los Angeles	Los Angeles	California

Sponsors (1)

Lead Sponsor	Collaborator
Jiangsu vcare pharmaceutical technology co., LTD

Countries where clinical trial is conducted

United States,  China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Inhibition of platelet aggregation [IPA] evaluated in healthy subjects to treatment with either vicagrel or clopidogrel	To compare IPA following multiple doses of vicagrel and/or clopidogrel in healthy subjects with different CYP2C19 phenotypes.	Day1-Day31
Primary	Platelet reactivity index [PRI] evaluated in healthy subjects to treatment with either vicagrel or clopidogrel	To compare PRI following multiple doses of vicagrel and/or clopidogrel in healthy subjects with different CYP2C19 phenotypes.	Day1-Day31
Primary	maximum plasma concentration (Cmax)	To compare Cmax following multiple doses of vicagrel and/or clopidogrel in healthy subjects with different CYP2C19 phenotypes.	Day1-Day31
Primary	Area under the curve over a dosing interval(AUC0-tau)	To compare AUC0-tau following multiple doses of vicagrel and/or clopidogrel in healthy subjects with different CYP2C19 phenotypes.	Day1-Day31
Secondary	Assess the safety and tolerability of multiple doses of both drugs in each CYP2C19 phenotype group.		Day1-Day31