Drug intelligence / Profile preview

budigalimab + rovalpituzumab tesirine

Development stage
Phase 1
Lead developer
AbbVie
Modality
Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

**Budigalimab + rovalpituzumab tesirine** is a combination therapy investigated for advanced solid tumors, especially small cell lung cancer (SCLC)[3][1][7][5][9]. Budigalimab is a humanized IgG1 monoclonal antibody that targets the programmed cell death 1 (PD-1) receptor on T-cells, functioning as an immune checkpoint inhibitor by blocking PD-1/PD-L1 interactions and reactivating exhausted T-cells for anti-tumor effects[2][3][4][8]. Rovalpituzumab tesirine is an antibody-drug conjugate (ADC) targeting delta-like protein 3 (DLL3), a protein highly expressed on SCLC cells. Rovalpituzumab tesirine delivers a cytotoxic payload directly to DLL3-expressing tumor cells, resulting in cell death. The combination was tested in the NCT03000257 phase I clinical trial, where patients received intravenous budigalimab and Rova-T infusions as separate agents for synergistic antitumor activity. While the combination demonstrated tolerability and clinical activity in SCLC, development of rovalpituzumab tesirine has since been discontinued due to evolving company strategies[3].

Other names
budigalimab + Rova-T
02

Targets

DLL3 (Delta-like ligand 3)PDCD1 (Programmed cell death protein 1 receptor)

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