Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
K2B-lead-PDC is an engineered SIRPα-based protein-drug conjugate (PDC) developed by K2B Therapeutics for the treatment of solid tumors. The drug is designed to target CD47, a transmembrane protein that acts as a "don't eat me" signal frequently overexpressed on cancer cells to evade phagocytosis. Unlike traditional anti-CD47 monoclonal antibodies, this PDC utilizes a modified SIRPα protein as the targeting moiety to deliver the cytotoxic payload monomethyl auristatin E (MMAE), a potent microtubule inhibitor. A key feature of the program is its "hit-and-run" pharmacology, which is intended to minimize the "sink effect" caused by CD47 expression on healthy red blood cells, thereby reducing the risk of hematologic toxicities such as anemia. The program was developed in partnership with the Korea Institute of Science and Technology (KIST) and is currently in preclinical stages.
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 K2B-lead-PDC.