XNW27011, a Claudin 18.2(CLDN18.2) targeted antibody-drug conjugate (ADC), in patients with CLDN18.2-positive gastric/gastroesophageal junction adenocarcinoma (G/GEJA): A phase 2 study.

3036 Background: The prognosis of G/GEJA remains poor, especially in late line patients (pts). mPFS for G/GEJA pts who received ≥ 2 prior lines of standard therapy is 1.6 - 2.6 months (mos). XNW27011 is a novel antibody-drug conjugate (ADC) targeting CLDN18.2, a promising therapeutic target that is aberrantly expressed in patients with G/GEJA. Methods: This phase 2 study aims to evaluate the efficacy and safety of XNW27011. Adult pt with advanced solid tumors who has failed standard therapy or is intolerable to available standard therapy/without available standard therapy, and with CLDN18.2 expression in ≥5% tumor cells (TC) with IHC staining ≥2+ (IHC≥2+, TC≥5%, EPR19202) were enrolled, including G/GEJA pts. All patients had measurable disease (RECIST v1.1) and ECOG 0-1. Patients received XNW27011 at 2.4-4.8 mg/kg Q3W. Endpoints included ORR for efficacy, TRAE events for safety and PK parameters. Results: As of Dec 29, 2025, a total of 86 eligible G/GEJA pts were enrolled at 2.4-4.8 mg/kg. IHC≥2+, TC≥20% was chosen as the CLDN18.2 expression criteria for further development of XNW27011. Here, we report the results in G/GEJA pts with CLDN18.2 expression of IHC≥2+, TC≥20%. Safety: 71 enrolled pts had CLDN18.2 expression of IHC≥2+, TC≥20%. The median age was 57.0 years, 87.3% of the pts had received ≥2 lines of systemic therapy, 85.9% of the pts had received immune checkpoint inhibitors. The common TRAEs (≥20%) included anemia, nausea, white blood cell count decreased, decreased appetite, neutrophil count decreased, vomiting, weight loss, hypoalbuminemia, asthenia, platelet count decreased, lymphocyte count decreased and hypokalemia. Efficacy: At 3.0 mg/kg, 26 patients were evaluable for efficacy, with 23 and 3 pts had received ≥2 and 1 prior lines of systemic therapy, respectively. The median follow-up(mFU) was 11.3 mos, cORR and cDCR were 65.4% and 84.6%, respectively. mPFS was 5.7 mos and mOS was 11.7 mos. Among the 23 pts who had ≥2 prior lines of therapy, the mPFS was 6.8 mos and mOS was 11.9 mos, with the mFU of 11.5 mos. Notably, one patient previously treated with CLDN18.2-targeted therapy still demonstrated durable clinical benefit, with PFS of 11.3 mos and still remains on treatment as of data cutoff date. Pharmacokinetics: At doses from 0.6 - 6.0 mg/kg in pts with solid tumors including G/GEJA, XNW27011 exposure (C max and AUC 0-∞ ) increased in an approximately dose proportional manner with a half-life of 5~7 days. Across all dose levels, circulating blood payload concentrations were low with 3.3% ADA positive rate. Conclusions: XNW27011 demonstrated promising anti-tumor activity and a manageable safety profile in CLDN18.2-positive G/GEJA. A pivotal phase 3 study evaluating XNW27011 as a ≥3 line therapy in G/GEJA pts is currently ongoing. Clinical trial information: NCT06792435 .

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Journal
Journal of Clinical Oncology
Published
2026-05-27
DOI
https://doi.org/10.1200/jco.2026.44.16_suppl.3036
Primary Topic
Barrier Structure and Function Studies
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article
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article

XNW27011, a Claudin 18.2(CLDN18.2) targeted antibody-drug conjugate (ADC), in patients with CLDN18.2-positive gastric/gastroesophageal junction adenocarcinoma (G/GEJA): A phase 2 study.

Guo Zeng-qing, Z.H. Liu, Zheng Hongxia, J Xia et al.
Journal of Clinical Oncology
Barrier Structure and Function Studies
article

XNW27011, a Claudin 18.2(CLDN18.2) targeted antibody-drug conjugate (ADC), in patients with CLDN18.2-positive gastric/gastroesophageal junction adenocarcinoma (G/GEJA): A phase 2 study.

Guo Zeng-qing, Z.H. Liu, Zheng Hongxia, J Xia, Feng Wang, Dongrun Zhu, Tianshu Liu, Qing Wen, Jingdong Zhang, Meili Sun, Hui Zhao, Lixin Wan, Linlin Wang, Jinming Yu, Dan Zhao, Jieer Ying, Fangling Ning, Jun Zhao, Ting Deng
article en

Abstract

3036 Background: The prognosis of G/GEJA remains poor, especially in late line patients (pts). mPFS for G/GEJA pts who received ≥ 2 prior lines of standard therapy is 1.6 - 2.6 months (mos). XNW27011 is a novel antibody-drug conjugate (ADC) targeting CLDN18.2, a promising therapeutic target that is aberrantly expressed in patients with G/GEJA. Methods: This phase 2 study aims to evaluate the efficacy and safety of XNW27011. Adult pt with advanced solid tumors who has failed standard therapy or is intolerable to available standard therapy/without available standard therapy, and with CLDN18.2 expression in ≥5% tumor cells (TC) with IHC staining ≥2+ (IHC≥2+, TC≥5%, EPR19202) were enrolled, including G/GEJA pts. All patients had measurable disease (RECIST v1.1) and ECOG 0-1. Patients received XNW27011 at 2.4-4.8 mg/kg Q3W. Endpoints included ORR for efficacy, TRAE events for safety and PK parameters. Results: As of Dec 29, 2025, a total of 86 eligible G/GEJA pts were enrolled at 2.4-4.8 mg/kg. IHC≥2+, TC≥20% was chosen as the CLDN18.2 expression criteria for further development of XNW27011. Here, we report the results in G/GEJA pts with CLDN18.2 expression of IHC≥2+, TC≥20%. Safety: 71 enrolled pts had CLDN18.2 expression of IHC≥2+, TC≥20%. The median age was 57.0 years, 87.3% of the pts had received ≥2 lines of systemic therapy, 85.9% of the pts had received immune checkpoint inhibitors. The common TRAEs (≥20%) included anemia, nausea, white blood cell count decreased, decreased appetite, neutrophil count decreased, vomiting, weight loss, hypoalbuminemia, asthenia, platelet count decreased, lymphocyte count decreased and hypokalemia. Efficacy: At 3.0 mg/kg, 26 patients were evaluable for efficacy, with 23 and 3 pts had received ≥2 and 1 prior lines of systemic therapy, respectively. The median follow-up(mFU) was 11.3 mos, cORR and cDCR were 65.4% and 84.6%, respectively. mPFS was 5.7 mos and mOS was 11.7 mos. Among the 23 pts who had ≥2 prior lines of therapy, the mPFS was 6.8 mos and mOS was 11.9 mos, with the mFU of 11.5 mos. Notably, one patient previously treated with CLDN18.2-targeted therapy still demonstrated durable clinical benefit, with PFS of 11.3 mos and still remains on treatment as of data cutoff date. Pharmacokinetics: At doses from 0.6 - 6.0 mg/kg in pts with solid tumors including G/GEJA, XNW27011 exposure (C max and AUC 0-∞ ) increased in an approximately dose proportional manner with a half-life of 5~7 days. Across all dose levels, circulating blood payload concentrations were low with 3.3% ADA positive rate. Conclusions: XNW27011 demonstrated promising anti-tumor activity and a manageable safety profile in CLDN18.2-positive G/GEJA. A pivotal phase 3 study evaluating XNW27011 as a ≥3 line therapy in G/GEJA pts is currently ongoing. Clinical trial information: NCT06792435 .

Journal of Clinical OncologyVol. 44(16_suppl)
Binzhou Medical University (CN), Shandong University of Aeronautics (CN), Sun Yat-sen University (CN), Changzhi Medical College (CN), Fudan University (CN), Tianjin Medical University Cancer Institute and Hospital (CN), Zhejiang Cancer Hospital (CN), Coherus BioSciences (United States) (US), Jinan Central Hospital (CN), Nanyang Institute of Technology (CN), Hunan Cancer Hospital (CN), Zhongshan Hospital (CN), The First Affiliated Hospital, Sun Yat-sen University (CN), Fujian Provincial Cancer Hospital (CN), Affiliated Hospital of Shandong University of Traditional Chinese Medicine (CN), Liaoning Cancer Hospital & Institute (CN), Anyang Tumor Hospital (CN), Shandong First Medical University (CN)
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Barrier Structure and Function Studies
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