Condition: IgA Nephropathy (IgAN) · Sponsor: Haisco Pharmaceutical Group Co., Ltd.
This is a Phase II, multicenter, open-label study. Eligible subjects who have completed the HSK39297-202 study will be enrolled.Starting dose is 200 mg QD.Dose may be increased to 300 mg QD after 8-12 weeks of stable 200 mg QD therapy if 24-h urine protein excretion (UPE) remains \>1 g/24 h and no Grade ≥3 treatment-related adverse events (AEs) occur.After the treatment period, subjects will enter the 4-week safety follow-up period.
This description comes directly from the study's public registry record.
li fangqiong Li · +86028-67258840 · lifangq@haisco.com
Always discuss trial participation with your own doctor first.
| Peking University First Hospital | Beijing, China | Completed |
| Peking University First Hospital | Beijing, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07616700