Pharmacogenomic Study in Patients of Lung, Colorectal and Head/Neck Cancers Receiving Chemotherapy
1 other identifier
observational
70
1 country
1
Brief Summary
The purpose of this study is to look at several genes that might determine how the body processes the drugs used to treat lung, colorectal and head and neck cancers. The goal of this examination is to help investigators determine the proper dosage to give future cancer patients or to better predict which future patients will respond to particular drug therapies.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Feb 2006
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2006
CompletedFirst Submitted
Initial submission to the registry
March 1, 2007
CompletedFirst Posted
Study publicly available on registry
March 2, 2007
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2008
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2008
CompletedNovember 28, 2016
November 1, 2016
2.6 years
March 1, 2007
November 23, 2016
Conditions
Study Arms (3)
2
colorectal cancer patients
3
head and neck cancer patients
1
lung cancer patients
Eligibility Criteria
medical center
You may qualify if:
- Lung, Colorectal and Head and Neck Cancer Patients that have received or plan to receive chemotherapy as part of their treatment
You may not qualify if:
- Colorectal cancer patients that have never received or will not receive chemotherapy as part of their therapy
- Head and Neck cancer patients that have never received or will not receive chemotherapy as part of their treatment
- Patients with cancer types other than colorectal or head and neck
- Unable to give informed consent
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Kansas Medical Centerlead
- Paul J. Patton Trustcollaborator
Study Sites (1)
University of Kansas Medical Center
Kansas City, Kansas, 66160, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Yu-Jui Yvonne Wan, Ph.D.
University of Kansas Medical Center
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 1, 2007
First Posted
March 2, 2007
Study Start
February 1, 2006
Primary Completion
September 1, 2008
Study Completion
September 1, 2008
Last Updated
November 28, 2016
Record last verified: 2016-11