Study to Evaluate the Efficacy and Safety of MY008211A in Subjects with Primary Immunoglobulin a Nephropathy (IgAN)
NCT06687174 · Status: NOT_YET_RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 72
Last updated 2024-11-18
Summary
Efficacy and safety of MY008211A in IgAN patients
Conditions
- IgA Nephropathy (IgAN)
Interventions
- DRUG
-
MY008211A tablets
MY008211A BID
- DRUG
-
MY008211A tablets matched placebo
Matching placebo to MY008211A taken twice a day.
Sponsors & Collaborators
-
Wuhan Createrna Science and Technology Co., Ltd
lead INDUSTRY
Principal Investigators
-
Hong Zhang, PH.D. · Peking University First Hospital
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-12-31
- Primary Completion
- 2026-06-15
- Completion
- 2028-01-31
Countries
- China
Study Locations
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