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Study of Osimertinib With Carotuximab in Advanced, EGFR-mutated Non-Small Cell Lung Cancer

NCT05401110

This study is recruiting at 5 US sites in 1 state, according to its ClinicalTrials.gov record last updated .

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.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Non Small Cell Lung Cancer
  • Lung Cancer

Eligibility basics and study details

Study type
Interventional
Phase
Phase 1
Ages
18 years and older
Sex
All
Healthy volunteers
Not accepted
Sponsor
Karen Reckamp, MD, MS
Last updated on ClinicalTrials.gov
August 6, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

California · 5

  • Cedars-Sinai Cancer at Beverly Hills (THO) · Beverly Hills, CA
  • Cedars-Sinai Cancer at SOCC · Los Angeles, CA
  • Cedars-Sinai Cancer at The Angeles Clinic and Research Institute · Los Angeles, CA
  • Cedars-Sinai Medical Center · Los Angeles, CA
  • Cedars-Sinai Cancer at Hunt Cancer Center - TMPNCC · Torrance, CA

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.