Study on the Safety and Effectiveness of AZD5492, a T Cell-Engaging Antibody for Treating Relapsed or Refractory B-Cell Cancers

Sponsor: AstraZeneca

Sponsor score: 40
Inactive

ClinicalTrials ID:NCT06542250

This clinical trial is testing a new antibody treatment, AZD5492, to see if it is safe and effective for patients with B-cell cancers that have returned or not responded to previous treatments.

Patient Parameters

Program Overview

The purpose of this study is to determine if the experimental antibody AZD5492, which targets a protein called CD20 on B-cells, is safe and effective for patients with B-cell cancers that have come back or are not responding to other treatments. This study is in Phase I/II, which means it is early in the research process and aims to find out more about the safety and potential benefits of the treatment.

Eligibility Criteria

Inclusion Criteria

  • Must be 18 years or older.
  • Have a confirmed diagnosis of a CD20-positive B-cell cancer, such as:
    • Large B-cell lymphoma
    • Follicular lymphoma
    • Mantle cell lymphoma
    • Chronic lymphocytic leukemia
    • Small lymphocytic lymphoma
  • The cancer must have returned or not responded after at least two previous treatments.
  • Be in relatively good health with an ECOG performance status of 2 or lower, meaning fully active or able to do light work.

Note: Additional criteria may apply.

Exclusion Criteria

  • Have active cancer involvement in the brain or other central nervous system issues.
  • Have certain types of aggressive lymphomas, such as post-transplant lymphoproliferative disease, Richter's transformation, Burkitt's lymphoma, or Burkitt-like lymphoma.
  • Have had a stem cell transplant within the last 90 to 180 days, depending on the type, or cell therapy within the last 90 days.
  • Have a history of severe side effects from previous cancer treatments, such as high-grade cytokine release syndrome (CRS) or neurotoxicity (ICANS).
  • Have active and uncontrolled infections.
  • Have unresolved side effects from previous cancer treatments that are moderate or severe, with some exceptions.

Note: Additional criteria may apply.

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