A Clinical Trial to Assess Safety and Efficacy of Daratumumab in the Treatment of Primary Immune Thrombocytopenia

Last updated: February 20, 2025
Sponsor: Institute of Hematology & Blood Diseases Hospital, China
Overall Status: Active - Recruiting

Phase

2

Condition

Immune (Idiopathic) Thrombocytopenic Purpura (Itp)

Thrombosis

Thrombocytopenia And Thrombocytopenia Prevention

Treatment

Daratumumab Injection

Clinical Study ID

NCT05562882
IIT2022039（1）
2022-D-ITP
  • Ages > 18
  • All Genders

Study Summary

A single-center, open-label, off-label use investigator-initiated clinical study with safety run-in to explore the clinical activity and safety of daratumumab in adult ITP patients who have not responded adequately or relapsed after first-line treatment and at least one second-line therapy including rituximab and/or TPO-RA.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Male or female aged ≥18 years.

  • Diagnosed with ITP that has persisted for ≥3 months and with a platelet count of <30X 109/L measured within 2 days prior to inclusion.

  • Failure to achieve response or relapse after corticosteroid therapy, and at leastone second-line therapy including rituximab and/or TPO-RA.

  • If receiving emergency care for ITP, treatment should be stopped >2 weeks beforefirst dose.

  • A positive result to the ELISA test to detect antibody against GPIIb/IIIa orGPIIb/IIIa and GPIb/IX within 1 week prior to inclusion.

  • With normal hepatic and renal functions.

  • ECOG Performance Status ≤ 2.

February 16, 2023 After approval by the Ethics Committee on , subjects no longer require platelet glycoprotein autoantibodies positivity upon enrollment.

Exclusion

Exclusion Criteria:

  • Received any treatment of anti-CD38 antibody drug.

  • Has been diagnosed with malignancy and/or liver failure, heart failure and renalfailure.

  • Known previous infection or seropositivity for HIV, Hepatitis B, Hepatitis C,Cytomegalovirus, EB virus, Syphilis.

  • Any clinically overt hemorrhage.

  • Has been diagnosed with cardiac disease, arrhythmia and/or severe or uncontrollablehypertension

  • Known pulmonary embolism, thrombosis and/or atherosclerosis.

  • Has been received allogeneic stem cell transplantation or organ transplantation.

  • Patients with history of current or past psychiatric disease that might interferewith the ability to comply with the study protocol or give informed consent.

  • Pregnancy or lactation.

Study Design

Total Participants: 20
Treatment Group(s): 1
Primary Treatment: Daratumumab Injection
Phase: 2
Study Start date:
December 10, 2022
Estimated Completion Date:
December 31, 2025

Study Description

Primary immune thrombocytopenia is an autoimmune disease associated with a reduced peripheral blood platelet count. The first-line treatment is corticosteroids. Splenectomy, rituximab, and thrombopoietin receptor agonists (TPO RAs, such as Etrapopar and Romistine) are commonly used as second-line therapy. However, many of the treatments used achieve few lasting remissions. About 20% - 30% of patients have inadequate or no response to first-line and second-line treatment, and would develop into recurrent/refractory (r/r) ITP.

A branch of pathogenesis for ITP has been revealed that plasma cells secrete pathogenic antibodies directed against platelet and red blood cell antigens. Antiplatelet specific plasma cells have been detected in the spleen of patients with rituximab refractory ITP. In those refractory cases, persistent autoreactive long-lived plasma cells in the bone marrow could explain treatment failure.

Daratumumab, an anti-CD38 monoclonal antibody developed to target tumoral plasma cells in multiple myeloma, was recently found to be effective in antibody-mediated diseases, such as autoimmune cytopenia following hematopoietic stem cell transplantation, systemic lupus and also ITP.

This study will evaluate the safety and biologic activity of Daratumumab in r/r primary ITP who fail to respond to at least one previous second-line therapy. The study will enroll approximately 20 participants. This trial will be conducted in China. All participants will be followed for at least 16 weeks after the 8 weeks of treatment.

Connect with a study center

  • Chinese Academy of Medical Science and Blood Disease Hospital

    Tianjin, Tianjin 300020
    China

    Active - Recruiting

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