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 @ 11:47 PM
Ignite Modification Date:
2025-12-24 @ 11:47 PM
NCT ID:
NCT02084251
Eligibility Criteria:
Inclusion Criteria:
* Male or female volunteers, ages: between 18-45;
* Body weight： female \>= 45kg, male \>=50kg, BMI \>=19-24kg/m2
* Physical examination, blood routine, urine routine, liver and kidney function and related laboratory tests are normal or slightly abnormal but not clinically significant;
* Read, agree, and sign the informed consent;
* Be able to communicate with the investigator and finish the study according to the protocol.
Exclusion Criteria （anyone or more of the following):
* Allergic to the API or excipients used (citric acid, mannitol, Meta-Cresol);
* Experiencing clinically significant disease or surgery within 4 weeks before the study;
* Clinically significant disease history in systems including cardiovascular system, endocrine system, neutral system, immunology system, psychiatry，metabolic disorder;
* Disease history of gastrointestinal tract, liver, and kidney (for example, the Partial resection surgery in GI tract, liver, or kidney);
* Fever history within 3 days of the screening;
* Clinical significant abnormality found in laboratory tests (blood, urine routine test) within 2 weeks before study;
* ECG or vital signs is clinically significant abnormality as judged by the Investigator( systolic blood pressure \<90mmHg or ≥140mmHg; diastolic blood pressure\<60mmHg or ≥90mmHg; heart rate \<50bpm or \>100bpm);
* Antibody test for HIV, BsAg, C hepatitis, or Microspironema pallidum positive;
* Alcoholics or drink frequently within 6 months of trial (more than 14 unit of alcohol, in which 1 unit is 360mL beers, or 45 ml wine with 40% alcohol content, or 150mL port wine;
* Addicted to cigarette, tea, coffee or drugs;
* Have specific requirement for diets (or allergic to any food);
* Have been administered in the past 2 weeks with any drug (such as antibiotics, anticoagulant, diuretics) that might interfere the PK profile of drug/drug candidate to be used in this study;
* Participated in any clinical trial in the past 3 months;
* Donated blood of more than 360 ml in the past 3 months;
* Plan to be pregnant herself or his spouse in the next 6 months;
* Females administered with any oral contraceptive 30 days before the study or during the study;
* Females dosed with long acting estrogen or progestin (injections or implant) 6 months before the study or during the study;
* Females at childbearing age that had unprotected intercourse 14 days before the study or will have during the study;
* Female who is pregnant or nursing;
* Anybody who might not be able to complete the study, or considered not appropriate by the investigator.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT02084251
Study Brief:
Protocol Section:
NCT02084251