Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**Tafasitamab + lenalidomide + R-CHOP** is a pharmaceutical combination regimen comprising an anti-CD19 monoclonal antibody (tafasitamab), an immunomodulatory agent (lenalidomide), and the standard first-line chemotherapeutic protocol for diffuse large B-cell lymphoma (DLBCL) known as R-CHOP, which includes rituximab (anti-CD20 monoclonal antibody), cyclophosphamide, doxorubicin, vincristine, and prednisone[1][3][7].\nTafasitamab enhances immune response by increasing antibody-dependent cellular cytotoxicity (ADCC) and antibody-dependent cellular phagocytosis (ADCP) through its Fc-engineered structure, specifically targeting CD19 on B-cells[6]. Lenalidomide acts as an immunomodulatory agent, promoting NK cell activity and synergistically improving the efficacy of anti-CD19 therapy, while also exhibiting direct antineoplastic effects. The R-CHOP regimen utilizes cytotoxic and immunotherapeutic agents to target malignant B cells through distinct mechanisms.\nThis combination is being investigated as front-line therapy for untreated DLBCL in phase 3 clinical trials (frontMIND), following promising safety and efficacy data from earlier studies[1][3][7].
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 tafasitamab + lenalidomide + R-CHOP.