- Alfasigma USA has acquired the brand ZELNORM (tegaserod), a treatment for IBS-C, from Sloan Pharma S.à r.l.
- In early 2019, ZELNORM was approved for reintroduction by the FDA for the treatment of adult women less than 65 years of age with IBS-C.
- Alfasigma USA plans to relaunch the brand in the United States, making ZELNORM available by prescription in the coming weeks.
Bedminster, NJ, July 8, 2019 – Alfasigma USA, Inc. today announced it has acquired the brand ZELNORM, a prescription pharmaceutical treatment for irritable bowel syndrome with constipation (IBS-C), from Sloan Pharma S.à r.l., a subsidiary of US WorldMeds Holdings, LLC. Plans to relaunch ZELNORM in the United States are currently underway.
Originally approved in 2002 as the first prescription medication for IBS-C, ZELNORM was voluntarily withdrawn from the market in 2007 due to concerns regarding possible cardiovascular risk; however, the drug has remained available in the US through an expanded access program authorized by the FDA. In early 2019, ZELNORM was approved by the FDA for reintroduction for use in adult women (<65 years of age) with IBS-C. The approval to reintroduce ZELNORM came after a thorough safety review by the FDA and an FDA-assembled Gastrointestinal Drugs Advisory Committee (GIDAC). The evaluation consisted of a review of the clinical data from 29 placebo-controlled trials and post-marketing treatment outcomes data.
“We are excited by the opportunity to make ZELNORM once again available to healthcare providers to treat adult women in the US suffering from IBS-C” said Bryan Downey, President and Chief Executive Officer at Alfasigma USA. “There is a substantial unmet need for IBS-C therapies with reliable efficacy, comparable safety, and that help address the debilitating pain and bloating associated with the disease. We look forward to making this effective IBS-C treatment available to the patients who may benefit the most”.
ZELNORM is the only selective serotonin-4 (5-HT4) receptor agonist approved to treat IBS-C. It provides a unique treatment by targeting the 5-HT4 receptor at multiple neurons (sensory, motor, secretory motor) and smooth muscle cells in the gastrointestinal tract to induce contraction and relaxation, and decrease pain signaling.
“We believed in the value of ZELNORM and invested a tremendous amount of time and effort to receive FDA approval for reintroduction and support for the revised indication in March 2019. The commercial capabilities of Alfasigma USA make it the right organization to reintroduce ZELNORM to the US market”, stated Hans van Zoonen, Manager of the Switzerland Branch of Sloan Pharma, S.à r.l.
IBS is prevalent in 7-21% of adults worldwide and in 5-9% of US adults. Its prevalence has increased over the past several decades and is particularly high in adult female patients over 50 years of age. 1-5 IBS is associated with substantially impaired quality of life, including effects on lifestyle, daily activities, and sleep, as well as work absenteeism.
According to Mr. Downey, “The reintroduction of ZELNORM is a first step in fulfilling our promise to find prescription pharmaceutical opportunities for Alfasigma in the US. With ZELNORM, our Alfasigma corporate slogan ‘Pharmaceuticals with Passion’ is now as meaningful in the US as it is globally”.
Alfasigma USA looks forward to making ZELNORM available by prescription in the coming weeks. For more information, please see the Medication Guide and full Prescribing Information for ZELNORM at www.zelnormus.com.