Eligibility Module

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: 2025-12-26 @ 4:02 PM
Ignite Modification Date: 2025-12-26 @ 4:02 PM
NCT ID: NCT05781906
Eligibility Criteria: Inclusion Criteria: 1. Subjects who have voluntarily participated in the study and signed the informed consent form with good compliance; 2. Healthy male subjects aged 18-40 years (inclusive); 3. Subjects weighing ≥ 50 kg 4. Subjects in good health status Exclusion Criteria: 1. Subjects with a history of gastrointestinal surgery, renal surgery, cholecystectomy and other procedures that in the judgment of the investigator may affect drug absorption or excretion 2. hypersensitivity to the investigational product and its excipients 3. Subjects with diseases affecting the absorption, distribution, metabolism and excretion of oral drugs, 4. Subjects with fear of needles, hemophobia, difficulty collecting venous blood, or special requirements for diet, who cannot comply with uniform diet 5. Subjects who are abnormal with clinical significance for C-reactive protein or positive for coronavirus nucleic acid detection in coronavirus infection screening 6. Subjects who have participated in another clinical trial of other drugs and have received such investigational product within 3 months prior to the first dose 7. Having any other diseases or conditions that may affect the normal performance of the study or the evaluation of the study data, or having other conditions that are not suitable for the study, as judged by investigators
Healthy Volunteers: True
Sex: MALE
Minimum Age: 18 Years
Maximum Age: 40 Years
Study: NCT05781906
Study Brief:
Protocol Section: NCT05781906