Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This combination therapy consists of **peluntamig**, a first-in-class IgG-like bispecific antibody targeting DLL3 and CD47; **atezolizumab (Tecentriq)**, an anti-PD-L1 monoclonal antibody; **carboplatin**, a platinum-based chemotherapy agent; and **etoposide**, a topoisomerase II inhibitor. Peluntamig is developed by Phanes Therapeutics and acts by dual targeting DLL3 (a Notch pathway protein overexpressed on tumor cells) and CD47 (“don’t eat me” signal on cancer cells), aiming to enable immune recognition and attack of cancer cells. Atezolizumab blocks PD-L1, reactivating T-cells against tumors. Carboplatin forms DNA crosslinks leading to apoptosis, while etoposide inhibits DNA synthesis through topoisomerase II inhibition. The four-drug regimen is being evaluated for the treatment of extensive-stage small cell lung cancer, large cell neuroendocrine carcinoma of the lung, extrapulmonary neuroendocrine carcinomas, and treatment-emergent neuroendocrine prostate cancer in the SKYBRIDGE Phase I/II clinical trial[1][3][5][7].
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 + atezolizumab + carboplatin + etoposide.