The main purpose of this study is to evaluate the efficacy of MY008211A in PNH patients with residual anemia despite treatment with anti-C5 antibody.
This is a multicenter, single-arm, open-label phase III clinical trial. The purpose of this study is to determine whether MY008211A is efficacious and safe for the treatment of PNH patients Who Are Still Anemia After Anti-C5 Antibody Treatment.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
20
MY008211A tablets Participants will receive MY008211A at a dose of 400 mg orally b.i.d
Peking Union Medical College Hospital (PUMCH).
Beijing, Beijing Municipality, China
RECRUITINGThe proportion of Participants With Sustained Hemoglobin Levels of ≥ 120 g/L in the Absence of Red Blood Cell Transfusions (defined as no red blood cell infusion after D14 to D168)
The proportion of patients with sustained hemoglobin levels ≥ 120 g/L among those without RBC transfusion.
Time frame: between Day 126 and Day 168
The proportion of subjects with an increase in hemoglobin concentration ≥ 20 g/L from baseline among subjects who do not receive RBC transfusion (defined as no red blood cell infusion after D14 to D168)
Proportion of participants achieving a sustained increase from baseline in hemoglobin levels of ≥ 20 g/L assessed among those without RBC transfusion.
Time frame: between Day 126 and Day 168
Change From Baseline in Hemoglobin
Change in hemoglobin concentration from baseline in patients without RBC transfusion.
Time frame: between Day 126 and Day 168
The proportion of patients with LDH < 1.5 ULN among those without RBC transfusion.
The proportion of patients with hemolysis controlled (defined as LDH \< 1.5 ULN) among those without RBC transfusion.
Time frame: between Day 126 and Day 168
Change (Expressed as Percentages) in LDH level from baseline
Change (Expressed as Percentages) in LDH level from baseline
Time frame: between Day 126 and Day 168
Change in reticulocyte count from baseline
Change in reticulocyte count from baseline
Time frame: between Day 126 and Day 168
The proportion of patients without RBC transfusion
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The proportion of patients without RBC transfusion.
Time frame: between Day 14 and Day 168
Change in FACIT-F score from baseline
Change in FACIT-Fatigue score from baseline. The FACIT-Fatigue is a 13-item questionnaire with support for its validity and reliability in PNH that assesses patient self-reported fatigue and its impact on daily activities and function. All FACIT scales are scored so that a high score is better. As each of the 13 items of the FACIT-F Scale ranges from 0-4, the range of possible scores is 0-52, with 0 being the worst possible score and 52 the best.
Time frame: between Day 126 and Day 168
The Clinical BTH Rate
The Clinical BTH Rate
Time frame: between Day 1 and Day 168
The Major Adverse Vascular Events Rate
The Major Adverse Vascular Events Rate
Time frame: between Day 1 and Day 168