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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
Conditions
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