Clinical Trials Directory

Trials / Unknown

UnknownNCT03346811

Efficiency of Icotinib in Plasma ctDNA EGFR Mutation-positive Patients Diagnosed With Lung Cancer

Efficiency of Icotinib in Plasma ctDNA EGFR Mutation-positive Patients Diagnosed With Lung Cancer:a Single Arm,Multi-center,Open-label Study

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
120 (estimated)
Sponsor
Betta Pharmaceuticals Co., Ltd. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

this single arm,open-label,multi-center study is aimed to evaluate the efficiency of icotinib in plasma ctDNA EGFR mutation-positive patients diagnosed with lung cancer

Conditions

Interventions

TypeNameDescription
DRUGIcotinibPatients with plasma EGFR mutation-positive are arranged to receive icotinib with a dose of 125 mg three times per day, till progressive disease or unaccepted toxicity

Timeline

Start date
2017-11-18
Primary completion
2019-05-10
Completion
2020-03-10
First posted
2017-11-17
Last updated
2017-11-17

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03346811. Inclusion in this directory is not an endorsement.