NCT06001151

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

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:A Multi-center, Single-arm, Phase II Study
Qian Chu·Phase 2·ClinicalTrials.gov·drugRecruiting
View on ClinicalTrials.gov
Study focus
Drug/Device/Intervention
Cadonilimab
Study type
Interventional
Intervention type
drug
Sponsor & location
Primary sponsor
Qian Chu
Funder
Tongji Hospital
Location
Wuhan, China
Timeline & enrollment
Phase
Phase 2
Start date
Aug 07, 2023
End date
Aug 31, 2027
Enrollment
49 participants
Primary outcome

12-month progression-free-survival (PFS) rate

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.

ICD-10 classifications
Carcinoma in situ: Bronchus and lungSecondary malignant neoplasm of lungMalignant neoplasm: Lower lobe, bronchus or lungMalignant neoplasm: Bronchus or lung, unspecifiedMalignant neoplasm of bronchus and lung
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06001151
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06001151 through Pure Global AI's free database. This Phase 2 trial is sponsored by Qian Chu and is currently Recruiting. The study focuses on Carcinoma, Non-Small-Cell Lung. Target enrollment is 49 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.