Clinical trialPhase 1Completed
A Research Trial of High Dose Vitamin C and Chemotherapy for Metastatic Pancreatic Cancer
A Phase I Trial of Ascorbic Acid and Gemcitabine for the Treatment of Metastatic Pancreatic Cancer
- Outcome
- Finished, no results posted
- Phase
- Phase 1
- Status
- Completed
- Study type
- Interventional
- Start
- December 2009
- Expected end
- March 2013
- Enrollment
- 15 participants
- Sites
- 1
- Primary outcomes
- Blood cell counts (neutropenia, thrombocytopenia) and serum chemistries (liver function tests, creatinine)
- Sponsor
- Other
- Results posted
- No
- Last update
- 21 April 2017
These are registry fields. A trial card, with population, design, endpoints and result direction each tied to a quote, is not in the data yet.
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Brief summary public domain (ClinicalTrials.gov)
This study is designed to determine the maximum tolerated dose of vitamin C when given with a standard chemotherapy for people who have metastatic pancreatic cancer.
Detailed description public domain (ClinicalTrials.gov)
This is a phase I, dose-escalating study of ascorbic acid (vitamin C) designed to determine the maximum tolerated dose of vitamin C or, if well tolerated, the dose required to obtain a desired ascorbic acid plasma concentration. Because this is a phase I study, prospective subjects should have advanced disease (i.e., metastasis) and have failed other curative therapies (or, are unable to receive curative therapies due to comorbidities or stage of disease).
Papers 1
- Registry-listed results paperPharmacological ascorbate with gemcitabine for the control of metastatic and node-positive pancreatic cancer (PACMAN): … DOI 10.1007/s00280-013-2070-8↗
The registry lists these as results papers; in a hand check of 27 such links about 78% reported the trial’s results, so read the paper before treating it as the outcome.