Intravenous Vitamin C in Combination With Standard Chemotherapy for Pancreatic Cancer

Completed · Phase 1

Conditions studied: Metastatic Pancreatic Cancer

In brief

Eligible candidates will be adults with metastatic pancreatic cancer (confirmed diagnosis with pathology reports and measurable computed tomography (CT) or magnetic resonance imaging (MRI)). Participants must not be receiving any other concurrent chemotherapy, or radiation therapy. Full inclusion/exclusion criteria are available. History and physical examination, and laboratory and imaging analyses will be done within 14 days prior to registration. The three cohorts of subjects will receive 50, 75 or 100 grams of intravenous ascorbic acid, three times per week for 8 weeks. Subjects will also have co-administration of the chemotherapy medications, gemcitabine (intravenously) and erlotinib (orally). Approximately 9 to 18 participants will be enrolled in this Phase I study.

Key facts

Study ID
NCT00954525
Run by
Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University
People needed
14
Starts
2009-07-01
Expected to finish
2011-12-01
Last updated by the study team
2025-05-02

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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