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Active, Not Recruiting

NCT Number: NCT04398459

The Safety and Efficacy of Ibrutinib in Refractory/Relapsed Autoimmune Hemolytic Anemia

This is an open-label, single-arm study to evaluate the safety and efficacy of Ibrutinib in subjects with refractory/relapsed autoimmune hemolytic anemia.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

6 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Zhoukou Central Hospital, Zhoukou, Henan, China

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • ECOG ≤ 3
  • Age from 6 to 70.
  • Diagnosed with WAIHA or MAIHA.
  • Meets the criteria of relapsed / refractory AIHA.
  • Meets the criteria of DAT-negative AIHA without any other inherited or acquired hemolytic diseases, and previously treated effectively with glucocorticoids and rituximab.
  • Signed informed consent.
  • Organs in good function.

Exclusion criteria

  • Nursing woman
  • Active bacterial, virus, fungal or parasitic infection, including HIV infection, HbsAg and HBV DNA positive, HCV DNA positive, etc.
  • Diagnosed with cold agglutinin disease or cold agglutinin syndrome or paroxysmal cold hemoglobinuria.
  • Secondary AIHA caused by drugs or infection.
  • Received rituximab in 8 weeks before enrollment.
  • Previously received treatment with BTK inhibitor.
  • Previously received organ or stem cell transplantation.
  • Have a history of thrombosis or organ infarction.
  • Diagnosed with an active stage of connective tissue disease.
  • Have a history of lymphoproliferative tumors or any other malignant tumors.
  • Have other inherited or acquired hemolytic diseases.
  • Received low-molecular-weight heparin or warfarin within 1 week before enrollment or during the Ibrutinib treatment.
  • Received CYP3A4 Enzyme Inhibitors or Inducers within 1 week before enrollment or during the Ibrutinib treatment.
  • Have a history of mental illness.
  • Inability to understand or to follow study procedures.

Treatment and study plan

Ibrutinib

Drug

Each recruited subject will accept Ibrutinib treatment.

Other names: BTK inhibitor

Primary outcomes

  1. Overall response rate

    Time frame: within 12 weeks

Secondary outcomes

  1. Incidence of adverse events and severe adverse events

    Time frame: within 48 weeks

  2. Relapse free survival rate

    Time frame: within 48 weeks

Sponsors and collaborators

Lead sponsor

Institute of Hematology & Blood Diseases Hospital, China

Other

Registry information

Official study title

A Phase II, Multicenter, Open-label Trial to Determine the Safety and Efficacy of Ibrutinib in Refractory/Relapsed Autoimmune Hemolytic

Important dates

Study start
2020
Primary completion
2024
Study completion
2025
First posted
May 21, 2020
Registry last updated
Sep 25, 2024

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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