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Not Yet RecruitingNCT07390383

A Phase II Clinical Trial of LBL-024 Combination Drug in Patients With Advanced Solid Tumour[Substudy 04]

An Open-label, Multicenter, Phase II Clinical Study to Evaluate the Efficacy and Safety of LBL-024 in Combination With Other Drugs for the Treatment of Patients With Advanced Solid Tumour[Substudy Number 04]

Status
Not Yet Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
110 (estimated)
Sponsor
Nanjing Leads Biolabs Co.,Ltd · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

An Open-label, Multicenter, Phase II Clinical Study to Evaluate the Efficacy and Safety of LBL-024 in Combination With Other Drugs for the Treatment of Patients With Advanced Solid Tumour.

Detailed description

This trial is an open-label, multicenter, phase II clinical study of LBL-024 in combination with other drugs for the treatment of patients with locally advanced or metastatic adenocarcinoma of the gastric or gastroesophageal junction,to evaluate the efficacy and safety of LBL-024 combination therapy. This study will have a safety run-in period in which a small number of subjects will be enrolled to receive LBL-024 combination therapy.After the subjects completed the 21-day safety observation, the sponsor and investigator jointly assessed the safety and tolerability of the combination drugs. If safety and tolerability are good, the extension study of combination administration will be continued, the subjects will be continued to be enrolled, and the randomized, open, positive control trial design will be adopted.Subjects who meet the criteria will be randomly assigned to the experimental group and the control group in a ratio of 2: 1. This trial will enroll up to 110 subjects.

Conditions

Interventions

TypeNameDescription
DRUGLBL-024 for InjectionIntravenous infusion
DRUGCapecitabine tabletsOral administration
DRUGTislelizumab InjectionIntravenous infusion
DRUGOxaliplatin injectionIntravenous infusion

Timeline

Start date
2026-04-01
Primary completion
2028-05-30
Completion
2028-05-30
First posted
2026-02-05
Last updated
2026-04-01

Locations

6 sites across 1 country: China

Source: ClinicalTrials.gov record NCT07390383. Inclusion in this directory is not an endorsement.