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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01585675
Other study ID # 04-0688.cc
Secondary ID P50CA058187
Status Recruiting
Phase
First received
Last updated
Start date November 3, 2005
Est. completion date July 1, 2035

Study information

Verified date December 2023
Source University of Colorado, Denver
Contact Brandi Kubala
Phone 303-724-1657
Email brandi.kubala@cuanschutz.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The primary objective of the protocol is to develop a comprehensive specimen banking program from patients with lung cancer for future translation research, which will enable the investigators to detect lung cancer earlier, develop better therapies and explore screening and prevention strategies.


Description:

The aims of the study are as follows: 1) to continue to unravel the complex biology of lung cancer 2) to identify early detection and prognostic markers to guide therapeutic decision 3) to define markers of response and/or resistance to drug therapy, and 4) to identify new therapeutic and prevention targets.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date July 1, 2035
Est. primary completion date July 1, 2035
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: 1. Subjects who are undergoing further testing for the diagnosis or treatment of lung cancer. 2. Oral and written informed consent Exclusion Criteria: 1. Any individual who does not give oral and written consent for participation

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States University of Colorado Cancer Center Aurora Colorado

Sponsors (2)

Lead Sponsor Collaborator
University of Colorado, Denver National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Development of a comprehensive specimen banking program from patients with lung cancer for future translational research. No statistical analysis will be applied to the overall collection of samples. Rather, each project that utilized tissue bank resources will require an appropriate statistical plan to be submitted along with the initial tissue request. 6 years
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