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Clinical Trial Summary

The purpose of this study is to examine the combination of osimertinib and carotuximab to assess the safety and find the recommended dose for treatment of advanced EGFR-mutated non-small cell lung cancer (NSCLC). Safety and tolerability will be measured by the number of dose-limiting toxicities, according to National Cancer Institute Common Toxicity Criteria for Adverse Events (NCI CTCAE) Version 5, to find the maximum tolerated dose. The secondary objectives include evaluating the rate of objective response rate, duration of response, progression-free survival, and disease control rate, along with assessing biomarkers through tumor tissue and circulating tumor DNA.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05401110
Study type Interventional
Source Cedars-Sinai Medical Center
Contact Clinical Trial Recruitment Navigator
Phone 310-423-2133
Email cancer.trial.info@cshs.org
Status Recruiting
Phase Phase 1
Start date September 15, 2023
Completion date January 2026

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