Stopped: Suspended to recruitment following TSC review on efficacy and toxicities
The primary purpose of this study is to assess whether Acelarin (NUC-1031) is superior to gemcitabine in terms of overall survival for treatment of patients with metastatic pancreatic carcinoma. In addition disease progression, quality of life and comparative safety will be evaluated. Secondary objectives are to compare between the two treatment groups the following: * Progression Free Survival (PFS) * Radiological Response and disease control rate * Toxicity and safety * Quality of Life Additional, exploratory objectives are to discover and validate possible biomarkers to predict additional benefit of Acelarin (NUC-1031) over gemcitabine alone.
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Number of participants that have survived throughout treatment and also into follow-up, as measured by the primary cause of death and date of death CRFs.
Timeframe: 4 years