Status:
COMPLETED
Drug-Drug Interaction Study Between Henagliflozin Proline and Hydrochlorothiazide
Lead Sponsor:
Jiangsu HengRui Medicine Co., Ltd.
Conditions:
Diabetes in Adults
Eligibility:
MALE
18-40 years
Phase:
PHASE1
Brief Summary
A single-center, single-arm, open-label, multi-dose, three-period study was conducted in healthy Chinese volunteers.
Eligibility Criteria
Inclusion
- Healthy male;
- Age 18-40 (including threshold);
- Weight ≥ 50 kg, body mass index (BMI): 19.0\~26.0 kg/m2 (including critical value);
- 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;
- Be able to communicate well with the investigators and understand and comply with the requirements in this study.
Exclusion
- Those have allergic constitution, or those with a known history of allergies to study drug or their excipients
- 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.
- Hepatitis B surface antigen positive, hepatitis C antibody positive, HIV antibody positive, syphilis antibody positive;
- Previous history of urinary tract infection or genital infection;
- Previous history of hypoglycemia and other important diseases;
- Those who have used other experimental drugs or medical devices within 3 months before screening;
- 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;
- 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;
- Have used any drugs in two weeks prior to taking the study drug;
- Can not comply with the unified dietary arrangement;
- Alcohol abuse, or those who smoke more 5 cigarettes per day in the 6 months prior to screening;
- Positive alcohol breath test,or positive drug screening;
- 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;
- Subjects who are judged by researchers to be unsuitable for participating in this test.
Key Trial Info
Start Date :
August 28 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 10 2019
Estimated Enrollment :
12 Patients enrolled
Trial Details
Trial ID
NCT06083116
Start Date
August 28 2019
End Date
October 10 2019
Last Update
October 13 2023
Active Locations (1)
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1
Shanghai Xuhui Central Hospital
Shanghai, Shanghai Municipality, China, 200031