Gemcitabine
DrugGemcitabine, IV bolus administered weekly (weeks 1-6) at least 4 hours before that day's radiation therapy.
NCT Number: NCT00251355
The purpose of this study is to test a new treatment of pancreatic cancer that cannot be removed by surgery. This treatment is a Phase I dose escalation research study which will combine one drug at increasing doses with a fixed dose of a second drug and radiation therapy. The drug that will be used at increasing doses is gemcitabine whereas 5-fluorouracil will remain the same for all patients.
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Notify Me18 year–72 year
All sexes
Interventional
Phase 1
Brigham and Women's Hospital, Boston, Massachusetts, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Gemcitabine, IV bolus administered weekly (weeks 1-6) at least 4 hours before that day's radiation therapy.
5-FU via continuous IV infusion.
External Beam Radiotherapy (weeks 1-6), Monday through Friday.
Time frame: phase 1
Time frame: phase 1
Time frame: phase 1
Dana-Farber Cancer Institute
Other
A Phase I Study of Gemcitabine, 5-Fluorouracil, and Radiation Therapy in the Treatment of Locally Unresectable Non-Metastatic Pancreatic Cancer
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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