Zanubrutinib in Primary Cold Agglutinin Disease - Trial NCT06067048

Timeline & Enrollment

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