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 @ 12:45 AM
Ignite Modification Date:
2025-12-25 @ 12:45 AM
NCT ID:
NCT06846567
Eligibility Criteria:
Inclusion Criteria:
1. Sign the informed consent form before the trial and fully understand the trial content, procedures, and potential adverse reactions;
2. Be able to complete the study in accordance with the trial protocol requirements;
3. The subject (and their partner) is willing to voluntarily adopt effective contraceptive measures from screening until 6 months after the last administration of the study drug. Specific contraceptive measures are detailed in Appendix 3;
4. Male and female subjects aged 18-45 years (inclusive);
5. Male subjects must weigh no less than 50.0 kg, and female subjects must weigh no less than 45.0 kg. BMI = weight (kg) / height (m²), with a body mass index ranging from 19.0 to 26.0 kg/m² (inclusive).
Exclusion Criteria:
1. Average daily smoking of more than 5 cigarettes within the 3 months prior to screening;
2. Allergy to any component of the investigational product, or a history of drug, food, or other substance allergies, or a history of allergic diseases;
3. History of drug abuse and/or alcoholism (alcoholism defined as consuming more than 14 units of alcohol per week: 1 unit = 285 mL of beer, 25 mL of spirits, or 100 mL of wine); history of drug abuse or use of illicit drugs within the past 5 years;
4. Donation of blood or significant blood loss (\>450 mL) within the 3 months prior to screening;
5. Difficulty swallowing or a history of gastrointestinal, liver, or kidney diseases (regardless of cure status) or surgeries within the 6 months prior to screening that may affect drug absorption or excretion;
6. Use of strong inhibitors and/or inducers of hepatic metabolic enzymes (CYP1A2, 2B6, 2A6, 2C8, 2C19, 3A4, and 3A5) within 28 days prior to the first dose. Strong inhibitors include ciprofloxacin, clopidogrel, itraconazole, ketoconazole, ritonavir, troleandomycin, etc. Strong inducers include rifampicin, carbamazepine, phenytoin sodium, St. John's wort, etc. Use of inhibitors or inducers of absorption transporters (e.g., P-gp, BCRP, OATP) and efflux transporters within 28 days prior to the first dose. For details, refer to Appendix 4;
7. Use of any prescription drugs, over-the-counter drugs, health supplements, or herbal medicines within 14 days prior to the first dose;
8. Consumption of any caffeine-rich, xanthine-rich, or CYP3A4 metabolism-affecting foods/beverages (e.g., grapefruit, animal liver, coffee, tea, cola, chocolate, etc.) within 14 days prior to the first dose or during the trial, or engagement in strenuous exercise (e.g., strength training, aerobic training, soccer), or other factors that may affect drug absorption, distribution, metabolism, or excretion;
9. Significant changes in diet or exercise habits within 7 days prior to the first dose;
10. Participation in another clinical trial within the 3 months prior to screening (subjects who withdrew from the study before treatment, i.e., were not randomized or did not receive treatment, may be enrolled in this study);
11. Inability to tolerate high-fat meals or having special dietary requirements, and unwillingness to accept a standardized diet;
12. Abnormal vital signs during screening (ear temperature \<35.7°C or \>37.5°C; pulse \<60 bpm or \>100 bpm; systolic blood pressure \<90 mmHg or ≥140 mmHg, diastolic blood pressure \<60 mmHg or ≥90 mmHg);
13. Clinically significant abnormalities in 12-lead electrocardiogram (ECG);
14. Female subjects who are breastfeeding or have a positive pregnancy test during screening or the trial period;
15. Clinically significant abnormalities in clinical laboratory tests or other clinically significant diseases (including but not limited to gastrointestinal, renal, hepatic, neurological, hematological, endocrine, oncological, pulmonary, immunological, psychiatric, or cardiovascular diseases) identified prior to screening;
16. Positive screening results for viral hepatitis (including hepatitis B and C), HIV antibodies, or syphilis antibodies;
17. Occurrence of acute illness from the screening phase until before study drug administration;
18. Consumption of any alcohol-containing products within 24 hours prior to the first dose or a positive alcohol breath test;
19. Positive urine drug screening;
20. Inability to tolerate venipuncture or a history of needle or blood phobia;
21. Vaccination within 4 weeks prior to the first dose or planned vaccination during the study period;
22. Other conditions deemed by the investigator to make the subject unsuitable for participation in the clinical trial.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT06846567
Study Brief:
Protocol Section:
NCT06846567