Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
TF4 is a humanized, trivalent, bispecific monoclonal antibody (bsMAb) developed by Immunomedics (now part of Gilead Sciences) using the proprietary Dock-and-Lock (DNL) platform. It is specifically designed for pretargeted radioimmunotherapy (PT-RAIT) of CD20-expressing B-cell malignancies, such as non-Hodgkin's lymphoma. The molecule is a tri-Fab construct consisting of two Fab fragments derived from the anti-CD20 antibody veltuzumab (hA20) and one Fab fragment derived from the anti-histamine-succinyl-glycine (HSG) antibody m679. In a pretargeting clinical or preclinical setting, TF4 is administered first to saturate CD20 receptors on tumor cells. After a clearance period, a radiolabeled hapten-peptide (e.g., 90Y-IMP-288) is administered, which binds with high affinity to the HSG-binding site on the tumor-localized TF4, thereby delivering a concentrated dose of radiation to the tumor while sparing healthy tissues.
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 TF4.