Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Peluntamig (PT217) is a first-in-class, native IgG-like bispecific monoclonal antibody that targets both delta-like ligand 3 (DLL3) and CD47. It is being developed by Phanes Therapeutics for the treatment of small cell lung cancer (SCLC), neuroendocrine carcinoma (NEC), and neuroendocrine prostate cancer (NEPC). The drug exerts its anti-tumor effects through multiple mechanisms, including inhibition of DLL3 protein and CD47 antigen, stimulation of macrophage activity, and induction of antibody-dependent cell cytotoxicity. Peluntamig has received orphan drug designations for SCLC and NEC as well as fast track designations from the FDA for extensive-stage SCLC with disease progression after platinum chemotherapy and metastatic or treatment-emergent NEPC. Clinical trials are ongoing in the US and China, with development currently in phase 1/2 for SCLC and NEC[1][2][3][4][5].
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 peluntamig.