Phase 2 ivonescimab PD-1×VEGF bispecific antibody consolidation after SBRT in early NSCLC
- Trial ID
- NCT07594522 on ClinicalTrials.gov
- Cancer type
- Non-Small Cell Lung Cancer (NSCLC)
- Stage of research
- Exploratory
- Location
- Basking Ridge, Middletown, Montvale, Harrison, and Uniondale (NJ/NY) + Commack, NY
- Published in
- New in Oncology - June 4, 2026
Memorial Sloan Kettering Cancer Center is running I-PRECISE, a Phase 2 study asking whether adding ivonescimab after definitive stereotactic body radiotherapy (SBRT)—delivered with either photon or proton techniques—can improve outcomes for early-stage, unresectable non-small cell lung cancer (NSCLC). Patients receive SBRT as usual care, then start consolidation ivonescimab about 4–6 weeks later on 21-day cycles; ivonescimab is a dual-targeting bispecific antibody designed to block PD-1 immune checkpoint signaling and VEGF-mediated angiogenesis. The key population is early-stage NSCLC without EGFR or ALK alterations, a group where targeted TKIs are not relevant and relapse prevention after local therapy remains a major need. The scientific angle is the “local control + systemic immune/anti-angiogenic consolidation” strategy—conceptually analogous to how consolidation immunotherapy changed unresectable stage III NSCLC, but here tested after ablative SBRT in earlier-stage disease. Today’s care for medically inoperable early-stage NSCLC is curative-intent SBRT alone (photon or, in select centers, proton), with no widely adopted post-SBRT systemic consolidation standard.
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