| Eligibility |
Inclusion Criteria:
- Participants must meet all of the following inclusion criteria to be enrolled in the
study:
1. Before the test, voluntarily sign informed consent, fully understand the test
content, process and possible adverse reactions, and be able to complete the
study in accordance with the requirements of the test plan;
2. Chinese male and female subjects aged 18-45 years old (including 18 and 45 years
old);
3. The weight of male subjects is not less than 50.0kg, the weight of female
subjects is not less than 45.0kg, the body mass index (BMI = weight/height 2
(kg/m2)), the body mass index is in the range of 19.0~26.0 kg/m2 (including the
cut-off value).
Exclusion Criteria:
- One of the following conditions will be excluded:
1. (Consultation, systematic inquiry) The study physician considers it inappropriate
for participants to have past or present chronic or serious diseases of
cardiovascular, liver, kidney, respiratory, blood and lymphatic, endocrine,
immune, psychiatric, nervous, gastrointestinal, metabolic and skeletal systems;
2. Clinically significant abnormalities judged by clinicians during the screening
period, including physical examination, vital signs examination,
electrocardiogram or clinical laboratory examination;
3. (Check) male QTc interval greater than 450ms, female QTc interval greater than
470ms;
4. (consultation) past or current epilepsy or a history of seizures;
5. Patients with a history of cholestatic jaundice/hepatic insufficiency after
previous use of azithromycin;
6. (consultation) people who have a history of specific allergies (asthma, etc.) or
are currently suffering from allergic diseases (urticaria, eczema, etc.), or are
allergic to two or more drugs, foods such as milk or pollen, or are known to be
allergic to components or analogizes of this drug (such as azithromycin,
erythromycin, other macrolides or ketonolactones);
7. (consultation) have dysphagia or any history of gastrointestinal diseases that
affect drug absorption (such as stomach or small intestine resection, atrophic
gastritis, gastrointestinal bleeding, obstruction, etc.);
8. (consultation) patients with any disease that increases the risk of
gastrointestinal bleeding (such as acute gastritis or gastric and duodenal
ulcers);
9. (consultation) Patients with venous blood collection difficulties and a history
of fainting needles and fainting blood;
10. (consultation, examination) female subjects who are in pregnancy, breastfeeding
or pregnancy test results are positive;
11. (Consultation) Subjects (including male subjects) who have not taken effective
contraception within 14 days before the first dose, or who have a pregnancy,
sperm donation or egg donation plan within 6 months after the last dose, see
Appendix 2 for specific contraceptive methods;
12. (examination) Human immunodeficiency virus antibody (screening), hepatitis B
virus surface antigen test, hepatitis C virus antibody test, treponema pallidum
antibody any test result is positive;
13. (consultation, examination) have a history of drug abuse within five years, or
have used drugs within 3 months before screening, or urine drug screening
positive;
14. (consultation, examination) those who consumed an average of more than 14 units
of alcohol per week (1 unit =360 mL beer or 45 mL liquor with 40% alcohol or 150
mL wine) in the three months prior to screening, or those who could not stop
alcohol intake from 24 hours before medication to the completion of the blood
sample collection for that cycle, or those who tested positive for alcohol
breath;
15. (Consultation) Those who smoked more than 5 cigarettes per day on average in the
3 months before screening or used e-cigarette products or refused to stop smoking
(including e-cigarettes) during check-in;
16. (Consultation) patients with surgery or severe trauma that the investigator
determined would affect drug absorption, distribution, metabolism, or excretion,
or who are scheduled to be hospitalized for surgery, dental surgery, or
hospitalization during the study period;
17. Blood donation and/or component blood within 3 months before screening or planned
blood donation and/or component blood during the test period, or large blood loss
(>400mL, except for female physiological blood loss), or blood transfusion or use
of blood products;
18. Patients who have participated in any drug clinical trials and used drugs within
3 months before screening (consultation);
19. (Consultation) Those who have taken any drug that alters liver enzyme activity or
interacts with azithromycin (such as antacids, ergotamine or dihydroergotamine,
fluconazole, efavirenz, nefinavir, etc.) within 28 days before the first dose;
20. (Consultation) Those who have taken any prescription drugs (including vaccines)
within 14 days before the first dose;
21. (Consultation) Those who have taken any non-prescription drugs, Chinese herbs or
health products for the prevention and/or treatment of their own diseases within
14 days prior to the first medication;
22. (Consultation) 48 hours before the first dose until the end of the study, those
who cannot avoid eating a special diet (such as grapefruit and products
containing grapefruit components) or have vigorous exercise, or have other
factors affecting drug absorption, distribution, metabolism, excretion, etc.;
23. (Consultation) patients who cannot avoid consuming any food or drink rich in
caffeine or xanthines (such as coffee, tea, chocolate, cocoa, milk tea, etc.) 48
hours before taking the drug until the end of the study;
24. Subjects deemed unsuitable by other investigators.
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