Drug intelligence / Profile preview

tafasitamab + idelalisib

Development stage
Unknown
Lead developer
Incyte
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous, Oral
01

Overview

Tafasitamab + idelalisib is an investigational combination therapy for relapsed or refractory chronic lymphocytic leukemia (CLL), particularly in patients who have failed prior treatment with a Bruton's tyrosine kinase inhibitor[1][3][4]. **Tafasitamab** is a humanized monoclonal antibody targeting CD19, inducing programmed cell death in malignant B cells and enhancing immune responses through antibody-dependent cellular cytotoxicity (ADCC) and phagocytosis[5][7]. **Idelalisib** is a selective small molecule inhibitor of the delta isoform of phosphatidylinositol-4,5-bisphosphate 3-kinase (PI3Kδ), which is important for B-cell survival, trafficking, and proliferation[2]. The rationale for combination is to target malignant B cells via both direct immunologic killing (CD19) and inhibition of survival/proliferation signaling (PI3Kδ). Clinical studies suggest high overall response rates and undetectable minimal residual disease in a subset of patients with R/R CLL[1][3][4]. This regimen remains investigational and not yet approved for standard care.

Other names
tafasitamab-cxixidelalisib
02

Targets

CD19 (B lymphocyte antigen CD19)PIK3CD (Phosphatidylinositol 3-kinase delta)

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