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NCT06067048Not yet recruiting

Zanubrutinib in Primary Cold Agglutinin Disease

Phase II Trial of Zanubrutinib in Primary Cold Agglutinin Disease. CaZa Study
Stichting Hemato-Oncologie voor Volwassenen NederlandPhase 2ClinicalTrials.govdrug
Study focus
Disease/Condition
Lymphoma
Drug/Device/Intervention
Zanubrutinib Oral Capsule
Study type
Interventional
Intervention type
drug
Sponsor & location
Primary sponsor
Stichting Hemato-Oncologie voor Volwassenen Nederland
Location
Leuven,Roeselare,Kopenhagen,Odense,Amsterdam,Nijmegen,Rotterdam,Bergen,Oslo, Belgium,Denmark,Netherlands,Norway
Timeline & enrollment
Phase
Phase 2
Start date
Feb 01, 2024
End date
Nov 01, 2028
Enrollment
25 participants
Primary outcome

CAD response rate (PR or CR) after 6 cycles of zanubrutinib treatment

Summary

Cold agglutinin disease (CAD) is defined as a chronic autoimmune hemolytic anemia (AIHA) with
 a monospecific direct antiglobulin test (DAT) strongly positive for C3d and the presence of
 cold agglutinins (CA; titer ≥ 64 at 4°C). Patients may have a B-cell clonal
 lymphoproliferative disorder (LPD) detectable in blood or marrow but no clinical or
 radiological evidence of malignancy. CAD can lead to AIHA, peripheral ischemic symptoms
 (cold-induced peripheral symptoms such as acrocyanosis etc.), or both. The CAs are typically
 monoclonal IgM antibodies produced by the clonal B-cells, usually IgM kappa with specificity
 for the I antigen on erythrocytes. There is no curative treatment. Current treatment options
 include rituximab monotherapy, however this has only a limited and short-lasting effect.
 Rituximab in combination with chemotherapy induces deeper and more durable responses, however
 since CAD patients typically do not have an overt malignancy this comes with concerns about
 short- and long-term toxicity. Novel complement inhibitors may be effective for the hemolysis
 but are not expected to be effective against cold induced peripheral symptoms while this is
 directly IgM mediated. Bruton Tyrosine Kinase inhibitors (BTKis) are effective in many B-cell
 lymphoproliferative disorders including the IgM producing clone of Waldenström
 macroglobulinemia (WM) and were very effective on both AIHA and peripheral ischemic symptoms
 in patients with CAD based on retrospective data.

ICD-10 classifications
Hodgkin lymphomaFollicular lymphomaNon-Hodgkin lymphoma, unspecifiedFollicular lymphoma, unspecifiedHodgkin lymphoma, unspecified
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06067048
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06067048 through Pure Global AI's free database. This Phase 2 trial is sponsored by Stichting Hemato-Oncologie voor Volwassenen Nederland and is currently Not yet recruiting. The study focuses on Lymphoma. Target enrollment is 25 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.