Clinical trial

Study of Epirubicin (Pharmorubicin®), Carboplatin (Paraplatin®) and Capecitabine…

NCT00130936 · AHS Cancer Control Alberta, Other · Terminated

Key facts

NCT number NCT00130936
Title Study of Epirubicin (Pharmorubicin®), Carboplatin (Paraplatin®) and Capecitabine (Xeloda®) (ECC) in the Treatment of Unresectable Locally Advanced or Metastatic Gastric/Gastroesophageal Junction Cancer With Pharmacogenetic Correlates
Official title Combined Phase I/II Study of Epirubicin (Pharmorubicin®), Carboplatin (Paraplatin®) and Capecitabine (Xeloda®) (ECC) in the Treatment of Unresectable Locally Advanced or Metastatic Gastric/Gastroesophageal Junction Cancer With Pharmacogenetic Correlates
Lead sponsor AHS Cancer Control Alberta, Other
Status Terminated
Phase Phase 1/Phase 2
Study type Interventional
Conditions Gastric Cancer, Esophageal Cancer, Tumors
Intervention type Drug
Interventions Epirubicin, Carboplatin, Capecitabine
Enrollment 50
Start date Oct 1, 2005
Completion Nov 1, 2007
First posted Aug 17, 2005
Last update posted Feb 15, 2016
Countries Canada

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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