A Study to Learn About Dacomitinib in Patients With Non-small Cell Lung Cancer.
NCT ID: NCT06321510
Last Updated: 2025-07-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
29 participants
OBSERVATIONAL
2024-07-01
2025-12-31
Brief Summary
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This study is seeking participants who:
* have lung cancer that could not be controlled.
* have a type of gene called epidermoid growth factor receptor. A gene is a part of your DNA that has instructions for making things your body needs to work.
* have received dacomitinib for their lung cancer.
All participants in this study had received dacomitinib. Dacomitinib is a tablet that is taken by mouth at home. They continued to take dacomitnib until their cancer was no longer responding. The study will look at the experiences of people receiving the study medicine. This will help to see if the study medicine is safe and effective.
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Patients who were treated with dacomitinib as first-line treatment for advanced NSCLC during 01 October 2020 to 31 December 2022.
* Age ≥18 years old
* Evidence of a personally signed and dated informed consent document indicating that the patient (or a legally acceptable representative) has been informed of all pertinent aspects of the study.
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Pfizer
INDUSTRY
Responsible Party
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Principal Investigators
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Pfizer CT.gov Call Center
Role: STUDY_DIRECTOR
Pfizer
Locations
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Tri-Service General Hospital
Taipei, , Taiwan
Countries
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Related Links
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To obtain contact information for a study center near you, click here.
Other Identifiers
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NCT06321510
Identifier Type: REGISTRY
Identifier Source: secondary_id
A7471070
Identifier Type: -
Identifier Source: org_study_id
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