drugset / Trial / NCT06687174
Study to Evaluate the Efficacy and Safety of MY008211A in Subjects with Primary Immunoglobulin a Nephropathy (IgAN)
RandomizedParallel-groupTriple-blindTreatment
Summary
Efficacy and safety of MY008211A in IgAN patients
Timeline
- Start
- 2024-12-31
- Primary completion
- 2026-06-15
- Completion
- 2028-01-31
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | MY008211A | Unknown | 200 mg | — |
| Subject | MY008211A | Unknown | 400 mg | — |