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The following trials provide information to treat various types of gastrointestinal diseases, both for ongoing and completed clinical trials.  For more information on this therapy area please click here.

There are a number of ways to help you find trial information.  By using these filters you can find (i) recruiting status, (ii) therapy area, (iii) product and/or (iv) phase of drug development.  You can use one or all filters to identify your specific needs.

When a trial completes the results are reported here no later than one year after completion – this is why you may sometimes find that a Report is unavailable when you are searching through ‘closed’ trials.

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  • collapse A randomised, single blind, three-way cross-over, single-centre study to assess the pharmacodynamics (intragastric pH) and pharmacokinetics after repeated oral administration of D961H 20 and 40 mg, and omeprazole 20 mg in Japanese healthy male subjects
  • collapse A Phase III, Multicentre, Randomised, Double-blind, Parallel-group, Comparative Efficacy and Safety Study of D961H (20 mg once daily) Versus Placebo for the Prevention of Gastric and/or Duodenal Ulcers Associated with Daily Nonsteroidal Anti-inflammatory Drug (NSAIDs) Use
  • collapse A Phase I, Open-label, Randomized, Single-center, 2-stage Group Sequential Design, 2-way Crossover Bioequivalence Study Comparing a Fixed-dose Combination Capsule of Esomeprazole 40 mg and Low-dose Acetylsalicylic Acid 325 mg with a Free Combination of Esomeprazole Capsule 40 mg and Low-dose Acetylsalicylic Acid Tablet 325 mg After Single Oral Administration in Healthy Male and Female Subjects
  • collapse A Phase I, Open, Randomized, Single-centre, 3-way Crossover Drug-drug Interaction Study of Esomeprazole Capsule 40 mg and Low-dose Acetylsalicylic Acid Tablet 325 mg after 5 days Repeated Oral Administration in Healthy Male and Female Subjects
  • collapse A randomised, double-blind, double-dummy, parallel-group, activecontrolled, multicenter study to assess the efficacy and safety of esomeprazole 40 mg q12h i.v. or omeprazole 40 mg q12h iv administration for 5 days in subjects with acute non-variceal upper gastrointestinal bleeding
  • collapse A randomized, double-blind, parallel-group, placebo controlled study of esomeprazole iv (bolus infusion of 80 mg followed by a continuous infusion of 8 mg per hour) administered for 72 hours to assess prevention of rebleeding in patients that have undergone successful primary endoscopic haemostasis of a bleeding peptic ulcer – the PUB study
  • collapse A Multicenter, Randomized, Double-Blind, Placebo-Controlled Efficacy Study Comparing 4 Weeks of Treatment with Esomeprazole 20 mg qd and 40 mg qd to Placebo qd in Patients with Heartburn and Sleep Disturbances Associated with Gastroesophageal Reflux Disease (GERD)
  • collapse A Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Efficacy Study Comparing 4 Weeks of Treatment with Esomeprazole 20 mg qd to Placebo qd for the Resolution of Upper Abdominal Pain in Patients with Symptomatic Gastroesophageal Reflux Disease (sGERD)
  • collapse A 6-month randomized, double-blind, parallel-group, multicentre, placebo-controlled Phase II study to compare anti-asthmatic effect and safety of esomeprazole (Nexium) 40 mg twice daily or 40 mg once daily with placebo in adults with asthma
  • collapse Ulcer GU IV (discont NSAID)
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