Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
zanidatamab + capecitabine + tucatinib is an investigational combination regimen being studied for the treatment of HER2-positive cancers, particularly metastatic breast cancer. **Zanidatamab** is a bispecific monoclonal antibody that targets two distinct epitopes on the HER2 receptor, leading to dual HER2 blockade and enhanced antitumor activity. **Capecitabine** is an oral prodrug of 5-fluorouracil, a pyrimidine analog that disrupts DNA synthesis in dividing cells, classifying it as a cytotoxic antimetabolite. **Tucatinib** is a small molecule tyrosine kinase inhibitor that selectively inhibits the HER2 receptor, blocking downstream proliferative signaling. The combination aims for synergistic anti-HER2 activity by simultaneously interrupting HER2 signaling with zanidatamab and tucatinib, and inducing DNA damage with capecitabine. This drug regimen is under phase 1/2 study for HER2-positive solid tumors and as of this date has not received regulatory approval for any indication.
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 zanidatamab + capecitabine + tucatinib.