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Clinical Trial Summary

This study was designed to evaluate the efficacy and safety of cadonilimab (anti PD-1 and CTLA-4 bispecific antibody) in combination with pemetrexed and anlotinib for treatment of elderly patients with T790M-negative advanced non-squamous non-small cell lung cancer following resistance to EGFR-TKI.


Clinical Trial Description

This prospective study aims to enroll 20 elderly patients (ageā‰„65 years) with advanced non-squamous NSCLC with T790M negative after EGFR-TKI resistance. Eligible patients will be given 4 to 6 cycles of cadonilimab plus pemetrexed and anlotinib, followed by maintenance treatment with cadonilimab plus anlotinib until disease progression, intolerable toxicity, withdrawal of consent, death, or other protocol-specified causes, whichever occurs first. Imaging assessments are scheduled to conduct every 6 weeks for the first year and then every 12 weeks thereafter. The follow-up of participants who discontinued treatment for reasons unrelated to disease progression will be continued, until the initiation of other anti-tumor therapy, disease progression, death, or the end of the study, whichever occurrs first. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06277674
Study type Interventional
Source Guangzhou University of Traditional Chinese Medicine
Contact Fangfang Hou, Dr
Phone 86-020-81887233
Email 13527816095@163.com
Status Recruiting
Phase Phase 2
Start date November 2, 2023
Completion date June 2025

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