Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**TEV-56278 + pembrolizumab** is an investigational combination therapy for advanced and metastatic solid tumors, currently in Phase 1 clinical development. TEV-56278 is an anti-PD-1 antibody–interleukin-2 (IL-2) fusion protein (ATTENUKINE) designed to selectively deliver IL-2 cytokine stimulation specifically to PD-1–expressing T cells within the tumor microenvironment, thereby amplifying anti-tumor immune responses while reducing systemic toxicity[1][4][8]. Pembrolizumab, marketed as Keytruda, is a monoclonal antibody PD-1 inhibitor approved in numerous cancers; when combined, the therapeutics aim to synergistically activate and sustain T-cell mediated anti-tumor activity[6]. The combination is being developed by Teva and Fosun Pharma for cancers including melanoma and other solid tumors, with documented activities of tumor regression, enhanced T-cell infiltration, and durable immune memory in preclinical and early clinical studies[1][4][6][8].
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 TEV-56278 + pembrolizumab.