Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 9:41 PM
Ignite Modification Date:
2025-12-24 @ 9:41 PM
NCT ID:
NCT02817932
Eligibility Criteria:
Inclusion Criteria:
1. Healthy adult Korean or Caucasian males, 19 - 45 years of age
* Korean subjects: first generation of Korean subject born in Korea, both parents and the four grandparents must be of Korean origin. Proof of Korean ethnicity will be documented by medical interview and appropriate materials (e.g. Korean passport, Korean resident card) will be retained in the subject's folder
* Caucasian subjects: first generation of Caucasian subject, both parents and the four grandparents of European descent. Documentation of ethnicity will be by medical interview and by appropriate materials (e.g. passport, birth certificate(if not available, a signed affirmation by the subjects)) will be retained in the subject's folder
2. Subjects weighing ≥ 50 kg with BMI between 18 and 27 kg/m2 (inclusive) at screening visit
3. Subjects with no clinically significant abnormal findings as determined by physical examination, ECG, medical history, or clinical laboratory test results
4. Subjects who agreed to voluntarily participate in this study and comply with all the study requirements by signing informed consent form after being informed of the nature of this study and understanding all aspects of this study
Exclusion Criteria:
1. History of clinically significant gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorder
2. Surgery of the gastrointestinal tract that could interfere with kinetics of the study drug
3. Relevant chronic or acute infections
4. History of relevant allergy/hypersensitivity (including allergy to the trial medication or its excipients)
5. Administration of any investigational products within 3 months from the first dose of the study drug (ranolazine PR)
6. History of participating other BE study or clinical trial within 3 months from the first dose of the study drug(ranolazine PR)
7. Any of the following vital sign abnormalities
* Systolic blood pressure: \<90 mmHg or \>140 mmHg
* Diastolic blood pressure: \<50 mmHg or \> 90 mmHg
* Pulse rate: \<50 bpm or \>90 bpm
8. Any of the following ECG abnormalities
* PR \> 210 msec
* QRS complex \> 120 msec
* QTcF \> 430 msec
9. Any finding in the physical examination deviating from normal and judged clinically significant by the investigator
10. Any laboratory value outside of the reference range that the investigator considers to be of clinical significance
11. Subjects who have donated blood or received blood transfusion within 90 days of participating in this study
12. Subjects who are positive for Hepatitis B, Hepatitis C, VDRL and HIV
13. Subjects who showed positive result in alcohol and drug abuse tests
14. Subjects who have smoked over 10 cigarettes until 90 days prior to the study initiation or who is not able to stop smoking throughout the hospitalization period
15. Subjects who took prescribed medications within 14 days or over-the-counter (OTC) medications within 7 days prior to the first dose of the study drug (ranolazine PR) or who have to take these medications during the study period
16. Subject who judged not eligible for study participation by investigator
Healthy Volunteers:
True
Sex:
MALE
Minimum Age:
19 Years
Maximum Age:
45 Years
Study:
NCT02817932
Study Brief:
Protocol Section:
NCT02817932