Abstract CT116: A first-in-human phase 1 study on the safety, PK, receptor occupancy, and pharmacodynamic markers of SPX-303, a first-in-class LILRB2×PD-L1 bispecific antibody
Abstract Background: Leukocyte immunoglobulin-like receptor B2 (LILRB2) suppresses immune cell activation, particularly within myeloid cells in the tumor microenvironment (TME), while the PD-1/PD-L1 axis serves as a key immune checkpoint that inhibits T-cell function. SPX-303 is a novel bispecific antibody designed to simultaneously block LILRB2 and PD-L1, thereby revitalizing antitumor immune responses. Here, we present initial findings from the ongoing first-in-human Phase 1 trial of SPX-303 in patients with advanced solid tumors, including safety, pharmacokinetics (PK), and receptor occupancy (RO). Methods: This is an open-label, multicenter Phase 1 study for patients with advanced solid malignancies with 3+3 dose-escalation design, followed by an expansion cohort at the recommended Phase 2 dose (RP2D). SPX-303 is administered intravenously every three weeks and safety is assessed through CTCAE v5.0 criteria. Primary Objectives of this study are to determine the safety, tolerability, and RP2D of SPX-303. Secondary endpoints include antitumor activity as well as characterization of the PK and PD of SPX-303. This study is currently open and enrolling in escalation cohorts. Citation Format: Justin Moser, Hao Xie, Yujie Zhao, Yousef Zakharia, Dongdong Li, Brandon William, Dinh-Duc Nguyen, Jack Hovey, Tiffany Li, Robert Cai, Jichun Ma, Jingdong Qin, Martin Siekierzycki, Anthony Haight, Hua Jin, Weiwei Mao, Kevin Bin Li, Gui-Dong Zhu. A first-in-human phase 1 study on the safety, PK, receptor occupancy, and pharmacodynamic markers of SPX-303, a first-in-class LILRB2×PD-L1 bispecific antibody [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 2 (Late-Breaking, Clinical Trial, and Invited Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_2):Abstract nr CT116.
Authors
- Anthony R. Haight (ORCID: https://orcid.org/0009-0005-5300-7163)
- Dongdong Li (ORCID: https://orcid.org/0009-0005-5133-4478)
- Hao Xie (ORCID: https://orcid.org/0000-0002-9640-4055)
- K. Li (ORCID: https://orcid.org/0009-0005-9434-1600)
- Yousef Zakharia (ORCID: https://orcid.org/0000-0001-9480-2626)
- Jingdong Qin
- Ji‐chun Ma (ORCID: https://orcid.org/0000-0002-6404-4497)
- Brandon William
- Hua Jin (ORCID: https://orcid.org/0000-0001-5478-4611)
- Dinh-Duc Nguyen (ORCID: https://orcid.org/0000-0001-9366-9253)
- Martin Siekierzycki
- Gui-Dong Zhu
- Robert Cai
- Yujie Zhao (ORCID: https://orcid.org/0000-0002-6702-6526)
- Weiwei Mao (ORCID: https://orcid.org/0009-0006-2517-2257)
- Tiffany Li (ORCID: https://orcid.org/0000-0003-1138-1489)
- Justin C. Moser (ORCID: https://orcid.org/0000-0002-4427-9387)
- Jack Hovey
Institutions
- Nemours Children’s Clinic (US)
- Mayo Clinic in Arizona (US)
- HonorHealth (US)
- Mayo Clinic in Florida (US)
Publication Details
- Journal
- Cancer Research
- Published
- 2025-04-25
- DOI
- https://doi.org/10.1158/1538-7445.am2025-ct116
- Primary Topic
- Monoclonal and Polyclonal Antibodies Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00