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A Phase II Single-Arm Study Evaluating the Efficacy of PD-1 Inhibitor Combined With Denosumab and Chemotherapy in Locally Advanced or Metastatic Non-Squamous Non-Small Cell Lung Cancer Patients With Driver Gene-Negative Status

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This is an interventional study to explore the efficacy and safety of denosumab combined chemotherapy and anti-PD-1/PD-L1 inhibitor in locally advanced or metastatic NSCLC.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• Histologically or cytologically confirmed locally advanced or metastatic non-squamous non-small cell lung cancer (NSCLC)

• Documented negative for EGFR/ALK/ROS1/BRAFV600E/RET/METex14 mutations by validated genomic testing, with no prior targeted therapy and no history of other malignancies

• No previous systemic therapy for advanced/metastatic disease

• At least one measurable lesion per RECIST v1.1

• Eastern Cooperative Oncology Group (ECOG) Performance Status 0-1

• No use of parathyroid hormone/derivatives, calcitonin, osteoprotegerin, mithramycin, or potassium supplements within the past 6 months

• Adequate organ and marrow function

Locations
Other Locations
China
The First Affiliated Hospital of China Medical University
RECRUITING
Shenyang
Contact Information
Primary
Zhang Chief Physician
zhangly1105@126.com
15909881516
Time Frame
Start Date: 2025-05-12
Estimated Completion Date: 2027-10-31
Participants
Target number of participants: 40
Treatments
Experimental: denosumab combined chemotherapy plus anti-PD-1/PD-L1 inhibitor
Sponsors
Leads: China Medical University, China

This content was sourced from clinicaltrials.gov