Cadonilimab (AK104) Plus Chemotherapy as First-line Treatment in Non-squamous Non-Small Cell Lung Cancer (NSCLC) Patients With Programmed Cell Death Ligand 1 (PD-L1) Negative

NCT06001151 · Status: RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 49

Last updated 2023-08-21

No results posted yet for this study

Summary

This is a single arm, multi-center clinical trial. Target population is advanced or metastatic non-squamous Non-Small Cell Lung Cancer (NSCLC) Patients with Programmed Cell Death Ligand 1 (PD-L1) negative, aiming to evaluate the efficacy and safety of the combination therapy of Cadonilimab and chemotherapy. Cadonilimab is a PD-1/CTLA-4 bi-specific antibody.

Conditions

  • Carcinoma, Non-Small-Cell Lung

Interventions

DRUG

Cadonilimab

Patients receive cadonilimab (10mg/kg) every 3 weeks.

DRUG

Pemetrexed

Patients receive pemetrexed (500mg/m2) every 3 weeks.

DRUG

Carboplatin

Patients receive carboplatin (AUC=5) every 3 weeks for 4 cycles.

Sponsors & Collaborators

  • Akeso Pharmaceuticals, Inc.

    collaborator OTHER
  • Qian Chu

    lead OTHER

Principal Investigators

  • Qian Chu · Tongji Hospital

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-08-07
Primary Completion
2025-08-31
Completion
2027-08-31

Countries

  • China

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06001151 on ClinicalTrials.gov