Since the sudden appearance of Helicobacter pylori in 1983, the perception of upper gastrointestinal tract diseases such as peptic ulcers has radically changed. The idea that most gastroduodenal diseases are infectious can indeed be called a paradigm shift. This ingenious idea, proposed by Warren and Marshall, marked what can be coined a revolutionary turnaround in the perception of upper gastrointestinal tract diseases. It is no doubt that the greatest discovery of the last century, tantamount to the discovery of hepatitis B and C virus strains that cause hepatitis, cirrhosis, and hepatocellular carcinoma, and is indeed an achievement that deserves the Nobel Prize. As a result, the treatments of peptic ulcers, said to be constitutional and destined to recur, have been transformed into treatments designed for infections. Most peptic ulcers, which have tormented humankind throughout our history, are now maladies that can be easily cured clinically. Japan is known for its universally high rate of stomach cancer; however, we are faced with the urgent need to clarify the relationship between H. pylori and stomach cancer. Various studies have brought to light that this bacteria does cause chronic gastritis, in particular, atrophic gastritis, but there is no sound evidence showing that it directly causes stomach cancer as of yet. Indeed, the WHO has established the epidemiological connection of the bacteria, but I think that this serves no proof of direct causal associations. The truth about the sequence of infection by H. pylori, atrophic gastritis, intestinal metaplasia, and finally stomach cancer must be ascertained in Japan for its troublingly high stomach cancer rate. Against this background, we set up the MAGIC Project to investigate the connections between H. pylori and gastritis or stomach cancer. MAGIC stands for ‘Mucosta Against Gastric Inflammation & Carcinogenesis’. The issue that must be resolved now is: ‘Does H. pylori infection cause stomach cancer directly, and can eliminating this bacteria cure atrophic gastritis and thus prevent stomach cancer?’ To date, numerous cytoprotective agents have been developed and used clinically, predominantly in Japan. In the age of the H. pylori, we find ourselves questioning the significance of these drugs, and unwillingly admitting the crisis of cytoprotective agents. In this ‘age’, we are thrust with the fundamentally grave task of questioning the roles these agents play, and if they are really needed. The answers to these questions must of course be based on evidence. The MAGIC Project therefore decided to take up rebamipide (Mucosta), the representative cytoprotective agent, and investigate its roles in the stomach cancer sequence, regarding: whether rebamipide is able to prevent inflammations caused by H. pylori; if it can help heal mucosal atrophy; and if, as a result, it can contribute to the prevention of stomach cancer in some way. Rebamipide suppresses or eliminates the production of active oxygen species and suppresses the release of inflammatory cytokines from H. pylori-infected gastric mucosa, thereby controlling gastric inflammation. This ambitious study aims to clarify if such actions contribute to the recovery of the gastric mucosa after elimination of the bacteria, and finally to the prevention of stomach cancer. This study was continued for 4 years, mostly in 20 facilities around the world. The results were presented at a conference held during the Digestive Disease Week (DDW) meeting in San Francisco in 2002. This Alimentary Pharmacology and Therapeutics supplement issue carries the proceedings of those presentations. Most of these presentations deal with fundamental studies, but all are directly connected to clinical efficacy, and thus are considered to contribute to evidence-based medicine. I would first like to express my gratitude to Professor Pounder of Alimentary Pharmacology and Therapeutics for helping with the editing of this issue, and my respects to the many researchers who continued working on these long-term studies. Finally, I would like to express my heartfelt thanks to Otsuka Pharmaceutical Co., Ltd. for supporting this project.