Lung Cancer Clinical Trial

A Study in the United States Using Electronic Medical Records (EMR) to Assess Effectiveness of Afatinib (Gilotrif) Following Pembrolizumab and Chemotherapy in the Treatment of Metastatic Squamous Cell Carcinoma of the Lung

Summary

This study aims to characterize the profile and outcomes for patients with Squamous Cell Carcinoma of the Lung (SqCC) who progress on 1L pembrolizumab in combination with platinum based chemotherapy and receive afatinib as second line (2L) therapy.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Diagnosis of squamous or mixed histology non-small cell lung cancer

Treated with pembrolizumab in combination with platinum-based chemotherapy as initial therapy for advanced or metastatic disease (stage IIIB or IV)

First cycle of pembrolizumab received after 06/01/2018
Permanently discontinued 1L pembrolizumab treatment

Initiated second-line treatment at least 3 months prior to the date of data collection, with either :

Afatinib
Any chemotherapy
Age ≥ 18 years

Exclusion Criteria:

-Received pembrolizumab in combination with platinum-based chemotherapy as part of an interventional clinical trial

Study is for people with:

Lung Cancer

Estimated Enrollment:

200

Study ID:

NCT04552535

Recruitment Status:

Completed

Sponsor:

Boehringer Ingelheim

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There is 1 Location for this study

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Cardinal Health Specialty Solutions
Dublin Ohio, 43017, United States

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Study is for people with:

Lung Cancer

Estimated Enrollment:

200

Study ID:

NCT04552535

Recruitment Status:

Completed

Sponsor:


Boehringer Ingelheim

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