Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Runimotamab is a bispecific monoclonal antibody developed by Genentech (a subsidiary of F. Hoffmann-La Roche) for the treatment of HER2-expressing solid tumors, including metastatic breast cancer, gastric cancer, and adenocarcinoma of the gastroesophageal junction. It functions as a T-cell dependent bispecific antibody that simultaneously binds to CD3 on T cells and HER2 on tumor cells, crosslinking cytotoxic T lymphocytes with HER2-expressing cancer cells. This mechanism results in potent CTL-mediated lysis of tumor cells through antibody-dependent cell cytotoxicity and direct stimulation of T lymphocytes[1][2][3][5]. Runimotamab was administered intravenously in clinical trials but has been discontinued in Phase I development for its primary indications[2].
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 runimotamab.