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
| Type | Name | Description |
|---|---|---|
| DRUG | Icotinib | Patients 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.