Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Adenoviral vector encoding lacZ + dendritic cells is an experimental cellular immunotherapy comprising autologous or allogeneic dendritic cells (DCs) that have been genetically modified (transduced) with a recombinant adenoviral vector carrying the *lacZ* gene. The *lacZ* gene encodes the enzyme beta-galactosidase, which in this context serves as a model tumor-associated antigen (TAA). The therapy leverages the potent antigen-presenting capabilities of dendritic cells to process and present beta-galactosidase-derived peptides via MHC molecules. This presentation is intended to prime and activate antigen-specific CD4+ and CD8+ T lymphocytes, as well as natural killer (NK) cells, to mount a robust immune response against cells expressing the target antigen. This construct is primarily utilized in preclinical oncology research to evaluate the mechanisms of gene-modified DC vaccines and to study the interplay between innate and adaptive immunity in anti-tumor responses.
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 adenoviral vector encoding lacZ + dendritic cells.