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Study identifier: NCT06792435 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

XNW27011 Study of Advanced Solid Tumor Subjects Who Failed Standard Therapies.

Condition: Pancreatic Adenocarcinoma Metastatic · Lung Cancer (NSCLC) · Ovarian Cancer  ·  Sponsor: Evopoint Biosciences Inc.

PhasePhase 1/Phase 2
Planned participants240
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a global, multi-center, open-label, Phase I/II first-in-human study of XNW27011 monotherapy as an investigational product (IP) in patients with locally advanced and/or metastatic solid tumors who have failed or are intolerant to standard therapies. XNW27011 is an antibody-drug conjugate (ADC) targeting Claudin 18.2 (CLDN18.2), a transmembrane protein important to tight junctions. The study consists of 2 parts: Part 1 is the dose-escalation phase (Phase I), and Part 2 is the does-expansion phase (Phase II). In phase I part of the study, approximately 42 patients with locally advanced and/or metastatic solid tumors will be enrolled, irrespective of CLDN18.2 expression. However, the most recently available tumor tissue specimen will be collected (if available) for a retrospective CLDN18.2 expression confirmation. In phase II part of the study, only patients with confirmed CLDN18.2 expression by IHC in the central laboratory will be enrolled.The phase II part of the study will consist of the following four groups,Up to three dose cohorts for each patient group are planned currently. Each dose cohort will include approximately 20 patients. Approximately 240 patients evaluable will be enrolled in Phase Ⅱ part of the study.

This description comes directly from the study's public registry record.

Talk to the study team

Yingjie Zhao  ·  +86 15172466243  ·  yingjie.zhao@evopointbio.com

zhenhao Ma  ·  +86 13325139290  ·  zhenhao.ma@evopointbio.com

Always discuss trial participation with your own doctor first.

Locations (1)

Affiliated Hospital of Shandong First Medical UniversityJinan, Shandong, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06792435