Drug pipeline
Full profile accessExplore the programs pursuing this target and their development progress.
- Drug candidates
- Developers
- Development stage
Target intelligence / Profile preview
Granzyme K (GZMK) is a serine protease primarily expressed in cytotoxic lymphocytes, including natural killer (NK) cells and cytotoxic T lymphocytes (CTLs), where it plays key roles in immune defense and immunoregulation. It induces apoptosis via caspase-independent mechanisms, cleaving substrates such as SET, Bid, Ape1, and p53. Extracellularly, it activates endothelial cells and modulates pro-inflammatory cytokine responses by cleaving and activating Protease Activated Receptor 1 (PAR-1) and enhancing LPS–CD14 complex formation, augmenting Toll-like receptor 4 signaling.
Serine protease-mediated cleavage of intracellular and extracellular substrates, leading to apoptosis and inflammatory signaling.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Explore the programs pursuing this target and their development progress.
Follow the clinical studies evaluating therapies directed at this target.
Compare approaches across drug candidates, modalities, and indications.
Investigate the research and source evidence behind target biology and development.
Explore patent activity around therapies and technologies addressing this target.
Connect target biology, drug development, and emerging evidence in your research.
See how Gosset can support your research on Granzyme K (GrK).