Clinical Trials Logo

Hypergastrinaemia clinical trials

View clinical trials related to Hypergastrinaemia.

Filter by:
  • None
  • Page 1

NCT ID: NCT01699113 Completed - Hypergastrinaemia Clinical Trials

Effects of YF476 and Rabeprazole on Gastric Function

Start date: August 2006
Phase: Phase 1
Study type: Interventional

The primary objectives are to find out in healthy subjects if: - YF476 prevents the ECL-cell hyperplasia induced by repeated doses of rabeprazole - a proton pump inhibitor; - YF476 also prevents rebound hyperacidity after stopping rabeprazole; and - YF476 by itself causes neither ECL-cell hyperplasia after repeated doses nor rebound hyperacidity after stopping YF476. The secondary objectives are to: - assess the safety and tolerability of YF476, alone and in combination with rabeprazole; - compare the effects of YF476, alone and in combination with rabeprazole, on serum gastrin and plasma CgA and SST; - assess if there is a pharmacokinetic interaction between YF476 and rabeprazole; - assess the pharmacokinetics of repeat doses of YF476 by itself; and - study the metabolism of YF476.

NCT ID: NCT01601418 Completed - Hypergastrinaemia Clinical Trials

Effect of Single Doses of YF476 on Stomach Acidity

Start date: October 2001
Phase: Phase 1
Study type: Interventional

The objective of the study was to assess the effect of a range of single oral doses of YF476 on pentagastrin-induced gastric acid output in healthy volunteers

NCT ID: NCT01601405 Completed - Hypergastrinaemia Clinical Trials

Effect of Repeated Doses of YF476 on Stomach Acidity

Start date: October 2001
Phase: Phase 1
Study type: Interventional

The objectives of the study were: 1. To show that a single dose of YF476 blocks gastrin receptors in healthy subjects 2. To show that YF476 retains its ability to block gastrin receptors after repeated dosing despite losing its ability to suppress gastric acidity.

NCT ID: NCT01339169 Completed - Clinical trials for Chronic Atrophic Gastritis

YF476 and Type I Gastric Carcinoids

Start date: January 4, 2011
Phase: Phase 2
Study type: Interventional

The aim of the study is to find out if the experimental medicine, YF476, can make gastric carcinoids, a rare type of stomach tumour, shrink and disappear. Gastric carcinoids occur mainly in patients with chronic atrophic gastritis (CAG), a condition in which the acid-producing cells in the lining of the stomach can't make acid. Acid production is controlled by gastrin, a hormone (chemical messenger) that's released into the bloodstream. If the stomach can't make acid, blood levels of gastrin rise. High blood levels of gastrin in patients with CAG can cause other cells (ECL cells) in the lining of the stomach to grow and, over the years, to give rise to gastric carcinoids. Gastric carcinoids are usually benign, but they can become malignant. Therefore, patients with CAG and gastric carcinoids have the inside of their stomach checked regularly, by gastroscopy, to see if the gastric carcinoids need removing surgically. A gastroscope is a thin (1 cm), flexible tube at end of which is a mini video camera, which enables the user to inspect the lining of the stomach and a 'snare' to take samples of tissue (biopsies). YF476 (netazepide) is a gastrin receptor antagonist (blocks the effects of gastrin), so it's a potential new medical treatment for gastric carcinoids in patients with CAG. Up to 10 of these patients will take YF476 daily for up to 12 weeks. If they benefit from that treatment, they may take YF476 daily for up to another 52 weeks. They'll make several outpatient visits for tests, including checks on the safety of YF476. At some of the visits, they'll have a gastroscopy. At each gastroscopy, the gastric carcinoids will be measured and biopsies taken for laboratory tests.