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:
2025-12-25 @ 2:42 AM
Ignite Modification Date:
2025-12-25 @ 2:42 AM
NCT ID:
NCT02165033
Eligibility Criteria:
Inclusion Criteria:
* Provision of signed written informed consent before enrollment into the study, ability to communicate with the investigators, and to understand and comply with the requirements of the study.
* Healthy adults, aged between 20 and 40 years old.
* Subjects with Body Mass Index (BMI) of \>=18.5 and \<=25.0 (BMI will be calculated as weight in kilogram \[kg\]/height in meters2 \[m2\]).
* Physically and mentally healthy subjects as confirmed by an interview, medical history, clinical examination, chest x-ray and electrocardiogram.
* Clinical laboratory test: within limit of normal range or acceptable to investigator.
Exclusion Criteria:
* History of drug or alcohol abuse within the past year.
* Medical history of severe drug allergy or sensitivity to analogous drug.
* Evidence of acute or chronic diseases or having undergone surgery from 4 weeks prior to Period I dosing.
* Evidence of any clinical significant renal, cardiovascular, hepatic, hematopoietic, neurological, pulmonary or gastrointestinal pathology. Creatinine \> 2UNL (upper normal limit); Liver enzymes \> 2UNL; Total bilirubin \> 2UNL.
* Planned vaccination during the time course of the study.
* Taking any clinical investigation drug from 2 months prior to Period I dosing.
* Use of any medication, including herb medicine from 4 weeks before dosing.
* Donation of 500mL of blood in the past 3 months prior to dosing or donation of 250mL of blood in the past 2 months prior to dosing.
* A positive Hepatitis B surface antigen or positive Hepatitis C antibody result.
* A positive test for HIV antibody.
* In screening subjects will be given training to ensure that subjects are able to correctly use the investigational products. If the subjects, the use of the investigational products lack of proficiency will not be included in this study.
* Students of National Defense Medical Center.
* For female subjects, if they meet any of the following criteria:
1. Lactating women
2. Positive pregnancy test (urine) at screening, or prior to dosing
3. Do not use adequate contraception during the study
4. Women taking oral contraceptives
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
20 Years
Maximum Age:
40 Years
Study:
NCT02165033
Study Brief:
Protocol Section:
NCT02165033