Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
PTPµ (Protein Tyrosine Phosphatase receptor type Mu, encoded by the PTPRM gene) is a cell adhesion molecule that is frequently proteolytically cleaved in cancer, particularly glioblastoma multiforme (GBM). The PTPµ-targeted agent is a peptide-based molecule designed to specifically bind to the extracellular fragment of PTPµ that remains on the surface of tumor cells or is present in the tumor microenvironment. Developed primarily by researchers at Case Western Reserve University, notably Susann Brady-Kalnay, these agents are being developed for two main purposes: intraoperative imaging (when conjugated to a fluorophore like IRDye800CW) to define tumor margins, and targeted therapy (when conjugated to cytotoxic payloads or used to inhibit PTPµ signaling). The agent exploits the fact that PTPµ is specifically cleaved and redistributed in glioma cells compared to normal brain tissue, providing high tumor-to-normal contrast.
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 PTPµ-targeted agent.