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RECRUITING
NCT07534033
PHASE2

Phase II Clinical Study of Probiotic LR607 in Patients With Non-Small Cell Lung Cancer

Sponsor: Zhujiang Hospital

View on ClinicalTrials.gov

Summary

The goal of this clinical trial is to understand whether Lactobacillus rhamnosus LR607 can enhance neoadjuvant chemoimmunotherapy for adult patients with non-small cell lung cancer. It will also evaluate the safety of LR607. The main questions it aims to answer include: Can LR607 improve the major pathological response of neoadjuvant chemoimmunotherapy? What is the relationship between LR607 combined with neoadjuvant chemoimmunotherapy and treatment-related adverse reactions? What changes occur in the gut microbiota composition at the species level and gut metabolites of subjects after LR607 treatment? Participants will: Take LR607 daily for 3 months Visit the hospital for check-ups and examinations every month Record their pathological response, tumor recurrence, and treatment-related adverse reactions

Official title: Probiotics With High Expression of DL-peptidase (LR607) Can Enhance the Efficacy of Chemoradiotherapy in Resectable Stage IIB-IIIB Non-small Cell Lung Cancer: a Single-arm, Open-label, Multicenter, Phase II Clinical Trial

Key Details

Gender

All

Age Range

18 Years - 80 Years

Study Type

INTERVENTIONAL

Enrollment

46

Start Date

2025-12-06

Completion Date

2027-12-23

Last Updated

2026-04-16

Healthy Volunteers

Yes

Interventions

DRUG

Probiotics combined with neoadjuvant chemoimmunotherapy

This clinical study aims to enhance efficacy by using functional probiotics selected from a Chinese food-grade probiotic library in combination with neoadjuvant chemoimmunotherapy.

Locations (1)

Zhu Jiang Hospital of Southern Medical University

Guangzhou, China