Anti-OX40 antibody BAT6026 in patients with advanced solid tumors: A multi-center phase I study

BAT6026 is a fully human IgG1 OX40 monoclonal antibody. This was a multicenter, open-label, dose escalation, and dose expansion phase I study of BAT6026 conducted in patients with advanced solid tumors who failed standard treatment. Patients received BAT6026 injections ranging from 0.01-10 mg/kg on day 1 of every 3 weeks (Q3W) in dose escalation. In dose expansion phase, 6 patients received 10 mg/kg BAT6026 (Q3W). Thirty patients were enrolled, with 24 in the dose escalation phase and 6 in the dose expansion phase. BAT6026 was generally well tolerated and demonstrated an adequate safety profile at doses ranging from 0.01 mg/kg and 10 mg/kg. In 26 patients who were efficacy evaluable, 10 of them achieved stable disease and the disease control rate (DCR) is 38.5%. Further studies including combined with other immunotherapies and some new drug delivery modality and regimen need to be investigated.

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Journal
iScience
Published
2025-03-22
DOI
https://doi.org/10.1016/j.isci.2025.112270
Citations
3
Primary Topic
Cancer Immunotherapy and Biomarkers
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article
Field-Weighted Citation Impact
3.14
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article

Anti-OX40 antibody BAT6026 in patients with advanced solid tumors: A multi-center phase I study

Huaqiang Zhou, Yubiao Guo, Long Tang, Yongsheng Li et al.
3 citations
iScience
Cancer Immunotherapy and Biomarkers
3.14
article

Anti-OX40 antibody BAT6026 in patients with advanced solid tumors: A multi-center phase I study

Huaqiang Zhou, Yubiao Guo, Long Tang, Yongsheng Li, Zhang Li, Yuxiang Ma, Gang Yuan, Ziyi Fu, Jin‐Chen Yu, Hongyun Zhao
article en
3 citations

Abstract

BAT6026 is a fully human IgG1 OX40 monoclonal antibody. This was a multicenter, open-label, dose escalation, and dose expansion phase I study of BAT6026 conducted in patients with advanced solid tumors who failed standard treatment. Patients received BAT6026 injections ranging from 0.01-10 mg/kg on day 1 of every 3 weeks (Q3W) in dose escalation. In dose expansion phase, 6 patients received 10 mg/kg BAT6026 (Q3W). Thirty patients were enrolled, with 24 in the dose escalation phase and 6 in the dose expansion phase. BAT6026 was generally well tolerated and demonstrated an adequate safety profile at doses ranging from 0.01 mg/kg and 10 mg/kg. In 26 patients who were efficacy evaluable, 10 of them achieved stable disease and the disease control rate (DCR) is 38.5%. Further studies including combined with other immunotherapies and some new drug delivery modality and regimen need to be investigated.

iScienceVol. 28(6)
Sun Yat-sen University (CN), Ta Solutions (China) (CN), The First Affiliated Hospital, Sun Yat-sen University (CN), Sun Yat-sen University Cancer Center (CN), Chongqing Cancer Hospital (CN)
Good health and well-being
Openalex Percentile: Top 9%
Cancer Immunotherapy and Biomarkers
3.14
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