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NOT YET RECRUITING
NCT06394713
PHASE1/PHASE2

A Study to Evaluate the Efficacy and Safety of QLF31907 Combination Therapy in Patients With Advanced Malignant Tumors

Sponsor: Qilu Pharmaceutical Co., Ltd.

View on ClinicalTrials.gov

Summary

This study is designed to evaluate the safety and efficacy of QLF31907 combination therapy in advanced malignant tumors.

Official title: A Phase 1b/2 Trial to Evaluate the Efficacy and Safety of QLF31907 (PD-L1/4-1BB Bi-specific Antibody) Combination Therapy in Patients With Advanced Malignant Tumors

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

60

Start Date

2024-06-15

Completion Date

2026-12-15

Last Updated

2024-05-01

Healthy Volunteers

No

Interventions

DRUG

QLF31907

intravenous administration, once every 3 weeks

DRUG

Irinotecan

intravenous administration, 125 mg/m2, d1 and d8, every 3 weeks

DRUG

Docetaxel

intravenous administration, 75mg/m2, d1, every 3 weeks