Clinical Trials Logo

Clinical Trial Summary

The purpose of this study is to test the safety of high dose omeprazole and see what effects that it has on patients with exocrine pancreatic cancer.


Clinical Trial Description

During this study patients will receive treatment of omeprazole at the dose depending on group enrollment - Group A will receive omeprazole 80 mg, twice a day for 14 days unless unacceptable toxicity - Group B, will receive omeprazole 20 mg, once a day for 14 days Patients will receive treatment for 2~3 weeks during the study, and 2 months of follow up. Total accrual is anticipated to take 2 years. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04930991
Study type Interventional
Source University of Oklahoma
Contact SCC IIT Office
Phone 405-271-8777
Email SCC-IIT-Office@ouhsc.edu
Status Recruiting
Phase Early Phase 1
Start date September 7, 2021
Completion date June 2025

See also
  Status Clinical Trial Phase
Recruiting NCT04011982 - PATAKESS Protocol : Clinical and Biological Analysis of Exocrine Pancreatic Tumors
Completed NCT01020006 - Study of Safety and Tolerability of PCI-27483 in Patients With Pancreatic Cancer Patients Receiving Treatment With Gemcitabine Phase 2
Recruiting NCT03485209 - Efficacy and Safety Study of Tisotumab Vedotin for Patients With Solid Tumors Phase 2