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Randomized Phase II Trial to Outline the Efficacy of Gemcitabine Containing Regimens (Gemcitabine/Carboplatin and Gemcitabine/Paclitaxel) When Used as Preoperative Chemotherapy In Patients With Stage I and II NSCLC
To evaluate the rate of complete pathological response after 3 cycles of gemcitabine containing chemotherapy.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon-Fri from 9AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Chapel Hill, North Carolina, United States
Start Date
June 1, 2001
Completion Date
July 1, 2006
Last Updated
January 26, 2007
77
Estimated participants
Gemcitabine
DRUG
Carboplatin
DRUG
Paclitaxel
DRUG
Lead Sponsor
Eli Lilly and Company
NCT03128008
NCT01671332
NCT00798720
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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