NCT04206787Completed
The Study Observes Afatinib as First-line Treatment in Patients With Epidermal Growth Factor Receptor (EGFR) Mutation-positive Advanced Non-small Cell Lung Cancer
Real-world Study on Afatinib as First-line Treatment in Patients With Epidermal Growth Factor Receptor (EGFR) Mutation-positive Advanced Non-small Cell Lung Cancer (NSCLC)
Source: ClinicalTrials.gov · Last updated 28 Feb 2025
Brief summary (registry, in English)
This study aims to observe the sequential strategy with afatinib as first-line treatment and to find the optimal treatment strategy for long-term chemotherapy-free regimens in Chinese patients with EGFR-mutated advanced NSCLC. Furthermore, this study can also assess the effectiveness and safety of afatinib as first-line treatment.
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 72 (actual)
- First submitted
- 11 Dec 2019
- Start date
- 20 May 2020
- Primary completion date
- 18 Dec 2023
- Lead sponsor
- Boehringer Ingelheim
- Diseases
- Lung cancer
- NCT number
- NCT04206787
What you commit to
- Study type: Observational
- Participants enrolled: 72
- From 20 May 2020 to the primary completion date, 18 Dec 2023
- 10 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patients who have received previous systemic therapy (previous adjuvant or neoadjuvant therapies are permitted)
- Patients with symptomatic brain metastases (patients with brain metastases, who were previously treated, are eligible provided they have asymptomatic brain metastasis for at least 4 weeks on stable doses of medication) at the start of afatinib treatment
- Patients with concurrent participation in an interventional oncology clinical trial during the first-line treatment phase or within the last 30 days prior to the first-line treatment phase. If patients join another interventional study during the period of second-line treatment or later-line treatment, this patient should not be excluded from this study
Who the study is looking for
- Patients who are diagnosed with locally advanced or metastatic NSCLC with EGFR sensitive mutation positive
- Patients who will initiate afatinib as first-line treatment for EGFR mutation-positive NSCLC
- Male and female patients with age ≥18 years
- Written informed consent per local regulatory requirement
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (10)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Peking Union Medical College Hospital Coordinator of this site? Confirm its status | Beijing | China | Unknown status |
| West China Hospital Coordinator of this site? Confirm its status | Chengdu | China | Unknown status |
| First Affiliated Hospital of Guangzhou Medical University Coordinator of this site? Confirm its status | Guangzhou | China | Unknown status |
| The First Afiliated Hospital, Sun Yet-sen University Coordinator of this site? Confirm its status | Guangzhou | China | Unknown status |
| Hainan Cancer Hospital Coordinator of this site? Confirm its status | Haikou | China | Unknown status |
| The First Affiliated Hospital, Zhejiang University Coordinator of this site? Confirm its status | Hangzhou | China | Unknown status |
| China Shenyang Chest Hospital Coordinator of this site? Confirm its status | Shenyang | China | Unknown status |
| Shenzhen People's Hospital Coordinator of this site? Confirm its status | Shenzhen | China | Unknown status |
| The First Affiliated Hospital of Zhengzhou Unviersity Coordinator of this site? Confirm its status | Zhengzhou | China | Unknown status |
| Zhongshan People's Hospital Coordinator of this site? Confirm its status | Zhongshan | China | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.