| Eligibility |
Inclusion Criteria:
All subjects are required to meet all of the following conditions
1. Voluntarily sign informed consent prior to the start of activities related to this
study, be able to understand the procedures and methods of this study, and be willing
to strictly follow the clinical trial protocol to complete this study;
2. Subjects (including their partners) are willing to have no family planning and
voluntarily take highly effective contraception within 6 months after the last study
drug administration;
3. Age range from 18 to 65 (including both ends) on the date of signing the informed
consent, both male and female;
4. Male subjects should weigh no less than 50 kg and female subjects should weigh no less
than 45 kg; Body mass index (BMI) 18-32 kg/m2 (including both ends);
5. Creatinine clearance (calculated by Cockcroft-Gault formula) =60 mL/min;
Subjects with normal liver function should also meet all of the following conditions:
6. The following demographic matching criteria must be met during screening:
1. Body weight was matched with that of the group with liver function impairment,
with an average of ±10 kg;
2. Age matching was performed between the group with liver function impairment, the
mean was ±10 years old;
3. Gender matching was performed with liver function impairment group, and the mean
was ±1 case;
Subjects with impaired liver function should also meet all of the following
conditions:
7. Chronic liver injury caused by primary liver diseases (such as hepatitis B, hepatitis
C, autoimmune hepatitis, alcoholic liver disease, etc.), liver insufficiency patients
with Child-Pugh grade A or B;
8. Cirrhosis was clinically diagnosed;
9. Stable medication regimen for liver dysfunction, complications and other concomitant
diseases for at least 14 days prior to taking the study drug, and no adjustment of
medication (including type, dosage or frequency of medication) is required; Or have
not used drugs;
Exclusion Criteria:
Subjects meeting any of the following exclusion criteria will not be enrolled in this study
1. Allergic constitution, including severe drug allergy or history of drug allergy, known
allergy to the study drug or any component of the study drug;
2. During the screening period, electrocardiogram showed QTc interphase (QTcF) >470 msec
for males and >480 msec for females (corrected according to Fridericia's standard);
3. A history of dysphagia or any gastrointestinal disorder affecting drug absorption,
including frequent nausea or vomiting due to any etiology;
4. Patients with severe infection, trauma, gastrointestinal surgery or other major
surgical operations within 4 weeks before screening;
5. Those who had been vaccinated within 14 days prior to screening or planned to be
vaccinated during the study period;
6. Those who donated blood or lost more than 200 mL of blood within 3 months prior to
screening, or intended to donate blood during the trial or within 1 month after the
trial;
7. A strong or medium acting inducer or inhibitor of CYP3A enzyme, a strong
P-glycoprotein (P-gp) inhibitor or inducer used within 1 month before screening;
8. D1 had taken a special diet (including dragon fruit, mango, grapefruit, and/or
xanthine diet, chocolate) and/or consumed excessive amounts of tea, coffee,
grapefruit/grapefruit juice and/or caffeinated beverages (more than 8 cups of 200 mL
per cup per day on average) in the 2 weeks prior to administration;
9. Binge drinkers in the 3 months preceding screening, i.e. those who consume more than
14 units of alcohol per week (1 unit = 360 mL beer, or 45 mL spirits with 40% alcohol
by volume, or 150 mL wine) or those who test positive for alcohol; Smokers who smoked
at least 10 cigarettes a day in the 3 months before screening;
10. Those who have a history of drug use, or drug abuse, or test positive for drug abuse;
11. Pregnant or lactating women or women of childbearing age who have tested positive for
pregnancy;
12. Patients who cannot tolerate venipunction or have a history of fainting needle and
fainting blood;
13. Those not suitable for inclusion for other reasons;
Subjects with normal liver function should be excluded if they meet any of the
following exclusion criteria:
14. History of liver injury;
15. Have been or are currently suffering from any clinically serious disease such as
circulatory system, endocrine system, nervous system, digestive system, respiratory
system, hematology, immunology, psychiatric and metabolic abnormalities, or any other
disease that may interfere with the test results;
16. Physical examination, vital signs, laboratory examination, 12-lead electrocardiogram,
abdominal color ultrasound and other abnormalities were judged by researchers to have
clinical significance;
17. Hepatitis B surface antigen, hepatitis C antibody or hepatitis C core antigen, HIV
antigen/antibody or syphilis antibody positive for any index;
18. Study the use of any prescription, over-the-counter, Chinese herbal or supplement
within 14 days prior to drug administration;
19. Use of other clinical trial drugs within 3 months prior to screening or plan to
participate in other clinical trials.
Subjects with liver function impairment who meet any of the following exclusion
criteria shall be excluded:
20. The subject has any of the following conditions: drug-induced liver injury; History of
liver transplantation; In addition, patients with cirrhosis that is considered to be
complicated by the following complications, including but not limited to liver
failure, hepatic encephalopathy, hepatocellular carcinoma, esophageal varicose
hemorrhage, etc.;
21. The laboratory test results during screening were consistent with any of the
following: (a) alanine aminotransferase (ALT) or aspartate aminotransferase (AST)
>10×ULN; (b) neutrophil absolute value (NE#) <0.75×109/L; (c) Hemoglobin (HGB) <60
g/L; (d) alpha-fetoprotein (AFP) >100 ng/mL;
22. HIV antigen/antibody screening positive; If syphilis antibody is positive, rapid
plasma rereaction hormone test (RPR) should be added. If RPR is positive at the same
time, it should be excluded.
23. In addition to the primary liver disease itself, those who have had or currently
suffered from other serious systemic organ diseases, including but not limited to
gastrointestinal, respiratory, kidney, nervous, blood, endocrine, tumor, immune,
psychiatric or cardiovascular and cerebrovascular diseases, or abnormal clinical
laboratory tests have clinical significance, and are judged by the study doctor to be
unfit to participate in this study;
24. Participants who used other clinical trials within 1 month prior to screening or
planned to participate in other clinical trials during the study period.
|
