Overview
Drug-Drug Interaction Study Between Henagliflozin Proline and Hydrochlorothiazide
Status:
Completed
Completed
Trial end date:
2019-10-10
2019-10-10
Target enrollment:
0
0
Participant gender:
Male
Male
Summary
A single-center, single-arm, open-label, multi-dose, three-period study was conducted in healthy Chinese volunteers.Phase:
Phase 1Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Jiangsu HengRui Medicine Co., Ltd.Treatments:
Hydrochlorothiazide
Criteria
Inclusion Criteria:1. Healthy male;
2. Age 18-40 (including threshold);
3. Weight ≥ 50 kg, body mass index (BMI): 19.0~26.0 kg/m2 (including critical value);
4. Volunteers (and their spouses) must not plan for childbearing or sperm donation within
one month prior to signing the informed consent form and from the period of taking the
research drug until three months after stopping it;
5. Be able to communicate well with the investigators and understand and comply with the
requirements in this study.
Exclusion Criteria:
1. Those have allergic constitution, or those with a known history of allergies to study
drug or their excipients
2. Physical examination, vital signs, blood-routine examination, blood biochemistry,
infectious disease screening, coagulation function, urine-routine examination, chest
x-ray, B ultrasound and other examination results are abnormal and judged by the
research doctor as clinically significant.
3. Hepatitis B surface antigen positive, hepatitis C antibody positive, HIV antibody
positive, syphilis antibody positive;
4. Previous history of urinary tract infection or genital infection;
5. Previous history of hypoglycemia and other important diseases;
6. Those who have used other experimental drugs or medical devices within 3 months before
screening;
7. Those who seek medical within 3 months prior to screening, which are judged by the
research doctor to be unfit for participants;Those who have undergone any surgery
within 6 months prior to screening;
8. Those who donate blood or other reasons of bleeding cause the total loss of blood more
than 400mL or receive blood transfusions within 3 months before screening;
9. Have used any drugs in two weeks prior to taking the study drug;
10. Can not comply with the unified dietary arrangement;
11. Alcohol abuse, or those who smoke more 5 cigarettes per day in the 6 months prior to
screening;
12. Positive alcohol breath test,or positive drug screening;
13. From 3 days before taking the study drug, subjects have xanthine-rich beverages or
food, or grapefruit and other fruits or juices that may affect metabolism;
14. Subjects who are judged by researchers to be unsuitable for participating in this
test.