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Clinical Trial Summary

The objective is to compare efficacy and safety of masitinib in combination with gemcitabine to placebo in combination with gemcitabine, in treatment of patients with locally advanced or metastatic pancreatic cancer and who have pain related to the disease.


Clinical Trial Description

Masitinib is a selective tyrosine kinase inhibitor that is thought to promote survival via modulation of immunostimulation-mediated anticancer effects and modulation of the tumor microenvironment. The objective of this study is to evaluate the efficacy and safety of masitinib in combination with gemcitabine with respect to placebo in combination with gemcitabine for the treatment of non resectable locally advanced or metastatic pancreatic cancer patients with pain related to the disease. Approximately 330 patients with pain Visual Analogue Scale (VAS) > 20 and/or treated with 'opioid analgesics' dose ≥ 1 mg/kg/day at baseline will be randomized in a 2:1 ratio to the masitinib and placebo arms, respectively. The primary outcome measure is overall survival (OS). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03766295
Study type Interventional
Source AB Science
Contact
Status Completed
Phase Phase 3
Start date July 2014
Completion date December 2020

See also
  Status Clinical Trial Phase
Recruiting NCT03579836 - Evaluation of Safety and Efficacy in BEY1107 in Monotherapy Gemcitabine Combination in Patient With Pancreatic Cancer Phase 1/Phase 2
Enrolling by invitation NCT03443492 - SLOG vs mFOLFIRINOX as the First-line Treatment in Locally Advanced Uncresectable or Metastatic Pancreatic Cancer Phase 2
Completed NCT00651742 - Phase 2 Study of S-1 in Advanced or Metastatic Pancreatic Cancer Phase 2
Completed NCT01181245 - A Phase 1 Study of Safety and Bioactivity With FG-3019 in Combination With Gemcitabine and Erlotinib for Subjects With Locally Advanced or Metastatic Pancreatic Cancer Phase 1