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A Study to Learn About Dacomitinib in Patients With Non-small Cell Lung Cancer. - Trial NCT06321510

Access comprehensive clinical trial information for NCT06321510 through Pure Global AI's free database. This phase not specified trial is sponsored by Pfizer and is currently Not yet recruiting. The study focuses on Lung Cancer. Target enrollment is 100 participants.

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NCT06321510
Not yet recruiting
Trial Details
ClinicalTrials.gov โ€ข NCT06321510
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A Study to Learn About Dacomitinib in Patients With Non-small Cell Lung Cancer.
Real-World Treatment Patterns and Clinical Effectiveness of Dacomitinib in Advanced Non-Small Cell Lung Cancer Patients With Epidermal Growth Factor Receptor-Positive in Taiwan

Study Focus

Lung Cancer

Observational

Sponsor & Location

Pfizer

Timeline & Enrollment

N/A

Apr 01, 2024

Mar 15, 2025

100 participants

Primary Outcome

Percentage of patients with dacomitinib dosage change and reasons,Percentage of patients with dacomitinib treatment discontinuation

Summary

The purpose of this study is to learn about dacomitinib for the possible treatment of lung
 cancer.
 
 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.

ICD-10 Classifications

Carcinoma in situ: Bronchus and lung
Secondary malignant neoplasm of lung
Malignant neoplasm of bronchus and lung
Malignant neoplasm: Bronchus or lung, unspecified
Malignant neoplasm: Overlapping lesion of bronchus and lung

Data Source

ClinicalTrials.gov

NCT06321510

Non-Device Trial