This is a multicenter, open-label study to evaluate the long-term safety, tolerability and efficacy of HSK39297. Adult patients with PNH who had previously received and completed HSK39297 study treatment will be included. Eligible subjects can maintain HSK39297 treatment until the end of the study.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
47
HSK39297 tablets until the end of treatment
The First Affiliated Hospital of Nanjing Medical University
Nanjing, Jiangsu, China
RECRUITINGIncidence and severity of adverse events
Time frame: through study completion,about 2 years
Proportion of participants achieving hemoglobin levels ≥ 12 g/dL in the absence of red blood cell transfusions
Time frame: through study completion,about 2 years
Change From Baseline in Hemoglobin in the absence of red blood cell transfusions
Time frame: through study completion,about 2 years
Proportion of participants who remain free from transfusions
Time frame: through study completion,about 2 years
Rate of breakthrough hemolysis (BTH)
Time frame: through study completion,about 2 years
Proportion of participants with Major Adverse Vascular Events (MAVEs)
Time frame: through study completion,about 2 years
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