Lung Cancer Clinical Trial

Clinical Trial Finder Lung Cancer Trials

A Prospective Longitudinal Collection of Subjects Diagnosed With Small Cell Lung Cancer

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Summary

The purpose of this study is to collect samples to evaluate the ProGRP and NSE assays independently as aids for monitoring the course of disease and therapy in subjects diagnosed with SCLC.

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Eligibility Criteria

Inclusion Criteria:

Age ≥ 18
Confirmed diagnosis of SCLC or mixed SCLC/non-SCLC per histopathology results
Scheduled to undergo first-, second- or third-line treatment for SCLC, including chemotherapy, chemotherapy + radiation therapy, or combined concurrent chemoradiotherapy.
Able to understand and willing to provide Informed Consent

Exclusion Criteria:

No diagnosis of SCLC
Not scheduled to undergo treatment for the diagnosis of SCLC
Unable to provide Informed Consent

Study is for people with:

Lung Cancer

Estimated Enrollment:

4

Study ID:

NCT01591512

Recruitment Status:

Terminated

Sponsor:

Fujirebio Diagnostics, Inc.

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There are 4 Locations for this study

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Kelly Family Medical Center, PC
Eastpointe Michigan, 48021, United States
St.Louis Cancer Care, LLP
Bridgeton Missouri, 63044, United States
Heartland Regional Medical Center
St. Joseph Missouri, 64506, United States
Hematology Oncology Consultants, Inc.
St. Louis Missouri, 63136, United States

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Estimated Enrollment:

4

Study ID:

NCT01591512

Recruitment Status:

Terminated

Sponsor:


Fujirebio Diagnostics, Inc.

How clear is this clinincal trial information?

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