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A Prospective Longitudinal Collection of Subjects Diagnosed With Small Cell
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.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Kelly Family Medical Center, PC
Eastpointe, Michigan, United States
St.Louis Cancer Care, LLP
Bridgeton, Missouri, United States
Heartland Regional Medical Center
Saint Joseph, Missouri, United States
Hematology Oncology Consultants, Inc.
St Louis, Missouri, United States
Start Date
May 1, 2011
Primary Completion Date
July 1, 2012
Completion Date
July 1, 2012
Last Updated
March 6, 2015
4
ACTUAL participants
Lead Sponsor
Fujirebio Diagnostics, Inc.
Collaborators
NCT06066138
NCT06305754
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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