Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
HB2198 is a trispecific antibody-based therapeutic developed by Hinge Bio, designed to achieve rapid and deep B cell depletion in both peripheral blood and lymphoid tissues. Its mechanism of action involves cooperative binding to CD19, CD20, and Fc gamma receptors (FcγR), enabling potent engagement of immune effector cells such as natural killer (NK) cells and monocytes. The drug leverages Hinge Bio’s proprietary GEM-DIMER platform, which creates multivalent, multispecific antibodies with enhanced biological activity compared to conventional monoclonal antibodies or CAR-T therapies. HB2198 aims for an “immune reset” in patients with autoimmune diseases by providing profound B cell depletion while maintaining the safety profile of off-the-shelf antibody therapeutics. Preclinical data suggest superior efficacy over existing antibody-based therapies for B cell-mediated diseases such as systemic lupus erythematosus (SLE), rheumatoid arthritis, B-cell lymphoma, and other B-cell malignancies[1][2][3][5][6][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 HB2198.