“Built to Wait. Wired to Strike.”
Conditionally active payloads that engage only when the environment is right.
Antibody-drug conjugates have revolutionized cancer therapy by enabling targeted delivery of potent cytotoxins. However, off-tumor toxicity remains a significant limitation, even for tumor-associated target antigens like MUC1 or Cathepsin B enriched in the TME.
Our epitope-based masking technology addresses this challenge by engineering a maskable peptide epitope that naturally blocks the antigen-binding site of the antibody until removed by tumor microenvironment (TME), while proteases cleave the mask and expose the active binding site.
Designed to specifically cover the epitope region of the antibody.
Cleaved by proteases like MMP2/9 or Cathepsin B enriched in the TME.
Once unmasked, the antibody binds its tumor antigen with full affinity.
Internalization and intracellular payload release follow naturally.