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NCT Number: NCT07151872

Combination of QLS31905 and Chemotherapy ± QL2107 in Patients With CLDN18.2-positive Advanced Biliary Tract Cancer

This is an open-label, multicenter Phase II clinical study aimed at evaluating the efficacy, safety, PK profile, and immunogenicity of QLS31905 for Injection combined with Chemotherapy ± QL2107 in Patients with CLDN18.2-positive Advanced Biliary Tract Cancer

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subjects with unresectable locally advanced or metastatic Biliary Tract Cancer confirmed by histopathological or cytological examination;
  • Subjects with at least one measurable lesion designated as a target lesion, as assessed by the investigator according to RECIST v1.1. Lesions that have received radiotherapy or other local treatments may be considered measurable if they demonstrate imaging PD;
  • No prior systemic anti-tumor treatment for locally advanced or metastatic Biliary Tract Cancer.

Exclusion criteria

  • Subjects with a known history of severe or repeated allergy, intolerance, or contraindication to QLS31905, QL2107, or other large molecule protein preparations, as well as Gemcitabine Hydrochloride for Injection, Cisplatin for Injection, Oxaliplatin Injection or Capecitabine Tablets and any components in their preparations;
  • Subjects had other second primary malignancies within 5 years prior to the first dose;
  • Subjects with clinically significant hemorrhage within 3 months before the first dose;

Treatment and study plan

QLS31905 for Injection

Drug

QLS31905 for Injection

Gemcitabine Hydrochloride for Injection

Drug

Gemcitabine Hydrochloride for Injection

Cisplatin for Injection

Drug

Cisplatin for Injection

QL2107 Injection

Drug

QL2107 Injection

Oxaliplatin injection

Drug

Oxaliplatin Injection

Capecitabine tablets

Drug

Capecitabine Tablets

Primary outcomes

  1. ORR (Objective Response Rate)

    Time frame: Approximately 24 months

    ORR is defined as the proportion of participants who have a best overall response of Complete Response (CR) or Partial Response (PR) as assessed by investigator per RECIST 1.1

Study contacts

Contact information is provided by the study sponsor or research team.

Tongsen Zheng, PHD

CONTACT

[email protected]

15134569619

Sponsors and collaborators

Lead sponsor

Qilu Pharmaceutical Co., Ltd.

Industry

Registry information

Official study title

A Phase II Clinical Study to Evaluate the Efficacy and Safety of QLS31905 for Injection in Combination With Chemotherapy ± QL2107 in Patients With CLDN18.2-positive Advanced Biliary Tract Cancer

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Sep 3, 2025
Registry last updated
Sep 3, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.