Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Tislelizumab + zanidatamab is an investigational combination therapy consisting of two monoclonal antibodies: tislelizumab, a humanized IgG4 anti-programmed death-1 (PD-1) immune checkpoint inhibitor, and zanidatamab, a bispecific antibody targeting two distinct extracellular domains of the human epidermal growth factor receptor 2 (HER2). Tislelizumab blocks PD-1 to enhance T-cell mediated antitumor immunity, while zanidatamab binds HER2 with biparatopic binding for dual signal blockade, increased receptor internalization and downregulation, and potent effector function. This combination is being studied primarily as first-line treatment for advanced or metastatic HER2-positive gastroesophageal adenocarcinoma in combination with chemotherapy. Early-phase studies have shown promising antitumor activity and manageable safety profiles[1][3][6].
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 tislelizumab + zanidatamab.