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: 2025-12-25 @ 1:23 AM
Ignite Modification Date: 2025-12-25 @ 1:23 AM
NCT ID: NCT06139393
Eligibility Criteria: Inclusion Criteria: 1. 18-75 years old, male or female; 2. BMI: 18.0-30.0 kg/m2; 3. Meet the 2015 ACR/EULAR gout classification criteria; 4. Fast serum uric acid ≥ 480 μmol/L on 2 different days during the screening perid; 5. Willing to ues contraceptive measures during the study; 6. Able and willing to provide a written informed consent. Exclusion Criteria: 1. History of acute gout attack within 4 weeks before randomization. 2. Subjects who have undergone major surgery or organ transplantation within 3 months before randomization. 3. Subjects with major cardiovascular disease within 6 months before randomization. 4. History of chronic infection or recurrent infection within 1year before randomization. 5. History of malignant tumor or current history of combined malignant tumor within 5 years before screening. 6. History of secondary hyperuricemia, refractory gout, or xanthine metabolism disorder. 7. Subjects with poorly controlled blood pressure or diabetes mellitus. 8. History of chronic diffuse connective tissue disease and/or massively elevated urate diseases and/or untreated clinically significant thyroid disease. 9. History of diseases that may affect the in vivo process, safety evaluation, or subjects' participation in the research. 10. Abnormal laboratory tests that may affect subjects participating in the research. 11. Combined use of prohibited drugs. 12. Allergic to ingredient or component of the experimental drug. 13. Participated in other clinical trials within 1 month before randomization. 14. Pregnant or nursing women. 15. History of drug abuse, drug use and/or excessive drinking within 1 year before screening. 16. The investigators determined that other conditions were inappropriate for participation in this clinical trial.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Maximum Age: 75 Years
Study: NCT06139393
Study Brief:
Protocol Section: NCT06139393