This is an open-label, single-arm study to evaluate the safety and efficacy of Ibrutinib in subjects with refractory/relapsed autoimmune hemolytic anemia.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
18
Each recruited subject will accept Ibrutinib treatment.
Zhoukou Central Hospital
Zhoukou, Henan, China
The Second Affilated Hospital of Shandong First Medical University
Tai’an, Shandong, China
Regenerative Medicine Center
Tianjin, Tianjin Municipality, China
Overall response rate
Time frame: within 12 weeks
Incidence of adverse events and severe adverse events
Time frame: within 48 weeks
Relapse free survival rate
Time frame: within 48 weeks
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