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Clinical Trial Summary

This is a prospective, randomised, uncontrolled phase II clinical trial planned to include 84 subjects with metastatic lung adenocarcinoma that had progressed after first- or second-line treatment with Osmertinib, who were randomly assigned to trial group 1 and trial group 2, and were given Furmonertinib 160 mg and 240 mg once/day, orally, respectively, with efficacy evaluated every 6 weeks until disease progression, intolerable toxic side effects, or Subjects voluntarily withdrew informed consent.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06394674
Study type Interventional
Source Changhai Hospital
Contact
Status Recruiting
Phase Phase 2
Start date May 2024
Completion date September 2026

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