Drug intelligence / Profile preview

TEV-56278 + pembrolizumab

Development stage
Unknown
Lead developer
Teva Pharmaceutical Industries
Modality
Immunomodulatory ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

**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].

Other names
pembrolizumab
02

Targets

PDCD1 (Programmed cell death protein 1 receptor)IL-2R (Interleukin-2/interleukin-15 receptor complex)

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