Ibrutinib
DrugEach recruited subject will accept Ibrutinib treatment.
Other names: BTK inhibitor
NCT Number: NCT04398459
This is an open-label, single-arm study to evaluate the safety and efficacy of Ibrutinib in subjects with refractory/relapsed autoimmune hemolytic anemia.
This study is active but is not currently recruiting participants.
Notify Me6 year–70 year
All sexes
Interventional
Phase 2
Zhoukou Central Hospital, Zhoukou, Henan, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Each recruited subject will accept Ibrutinib treatment.
Other names: BTK inhibitor
Time frame: within 12 weeks
Time frame: within 48 weeks
Time frame: within 48 weeks
Institute of Hematology & Blood Diseases Hospital, China
Other
A Phase II, Multicenter, Open-label Trial to Determine the Safety and Efficacy of Ibrutinib in Refractory/Relapsed Autoimmune Hemolytic
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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