Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
CD22 bispecific CAR-T cells are a form of chimeric antigen receptor T-cell therapy engineered to target both the CD19 and CD22 antigens on B-cell malignancies. These therapies are designed to overcome resistance and relapse associated with single-antigen targeting (such as loss of CD19 expression after standard anti-CD19 CAR-T therapy). The dual targeting is achieved by incorporating two single-chain variable fragments (scFvs) specific for both antigens into a single or tandem construct. This approach has shown robust cytolytic activity against B-cell acute lymphoblastic leukemia (B-ALL) in preclinical models and early-phase clinical trials. Both autologous (patient-derived) and allogeneic (donor-derived) versions have been developed. Clinical studies indicate that these therapies can induce high rates of minimal residual disease-negative complete remission in relapsed/refractory B-ALL patients[1][2][3][5][8].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on CD22 bispecific CAR-T cells.