Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**TAEK-VAC-HerBy + trastuzumab** is a combination immunotherapy regimen under clinical investigation for cancer. TAEK-VAC-HerBy is a first-in-class therapeutic cancer vaccine based on the non-replicating MVA-BN viral vector, encoding a membrane-bound form of human CD40L, a genetically modified HER2 (to prevent binding by trastuzumab and pertuzumab and preclude oncogenic activity), and a genetically modified form of the transcription factor Brachyury (to prevent its nuclear localization and oncogenic potential). Trastuzumab is a monoclonal antibody that targets the HER2 receptor, blocking its signal transduction and mediating antibody-dependent cell cytotoxicity. This combination is being studied for its potential to stimulate anti-tumor immunity in HER2- or Brachyury-expressing advanced cancers, especially HER2-positive breast and gastric cancers. The vaccine is designed for intravenous use, given together with trastuzumab, with or without pertuzumab, in relevant patient cohorts[1][2][3][4][5][7]. Developed and sponsored by Bavarian Nordic, the regimen is being tested primarily in adults with advanced or metastatic HER2-positive or Brachyury-expressing cancers.
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 TAEK-VAC-HerBy + trastuzumab.