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Axcan Receives FDA Approval Letter for Pylera for the Eradication of Helicobacter Pylori 

Axcan Receives FDA Approval Letter for Pylera, an Innovative 3-in-1 Capsule Triple Therapy for the Eradication of Helicobacter Pylori

MONT-SAINT-HILAIRE, Quebec, September 29, 2006 -- Axcan Pharma Inc. today announced that the US Food and Drug Administration (FDA) has issued an approval letter for the Company’s New Drug Application for Pylera (formerly Helizide). Pylera is a patented 3-in-1 capsule triple therapy, for the eradication of Helicobacter pylori, which is a bacterium now recognized as being the main cause of gastric and duodenal ulcers. Each Pylera capsule contains biskalcitrate potassium (140 mg), metronidazole (125 mg) and tetracycline hydrochloride (125 mg). The U.S. patent on the Pylera capsule technology expires in December 2018.

"We are pleased that the FDA has granted us final approval for Pylera, since our studies confirmed that Pylera is not only as effective as the most widely prescribed therapeutic regimen for the eradication of Helicobacter pylori (omeprazole, amoxicillin and clarithromycin), but that it has the potential to be used in a wide range of patients as a first-line therapy for the eradication of Helicobacter pylori," said Frank Verwiel, M.D., President and Chief Executive Officer of Axcan. "The US market for therapies for the eradication of Helicobacter pylori is in excess of US$160 million, and because of under diagnosis there is significant growth potential for this market. We are looking forward to entering this market with our innovative product, which should bring a clinical benefit by improving patient compliance. We anticipate launching Pylera in the United States in the first half of calendar 2007 and are working on preparing for the filing of this product in the European Union. With the approval of Pylera, we will have a total of 20 marketed products, and we believe that Pylera will add value to the portfolio of products we market, thus further strengthening our already solid base business."

Phase III Clinical Studies

The Phase III North American trials conducted in 275 patients with a history of duodenal ulcer compared Axcan’s Pylera regimen given in combination with two daily doses of 20 mg of omeprazole, to the widely used OAC triple therapy (20 mg of omeprazole, 1 g of amoxicillin and 500 mg of clarithromycin, all given twice a day). On an intent-to-treat basis, the eradication rates, although not statistically significant, were 88% and 83%, respectively, in favor of Pylera.

About Helicobacter pylori

The discovery in 1983 of the Helicobacter pylori organism was one of the major advances in gastroenterology in recent decades, as it revolutionized the approach to many upper gastrointestinal disorders. Helicobacter pylori is now recognized as one of the most important causes of gastric and duodenal ulcers, which affect at least 10% of the North American population at one point in their lives. It is believed to cause a spectrum of diseases in humans, including gastritis, ulcer disease (gastric and duodenal), gastric cancer, and gastric lymphoma. Existing ulcer treatment regimens lead to high recurrence rates. Gastric and duodenal ulcers recur respectively in approximately 40% to 80% of patients within a year after having received short-term treatment with acid suppression therapy. Studies have shown that the recurrence rate of peptic ulcers after one year is only 2% in patients in whom the organism has been eradicated.

Source: Axcan Pharma Inc.

Posted: September 2006


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