Press Release
Press Release
The global binge eating disorder market is expected to be driven by growing awareness of the condition and development of treatments for the disorder. The increasing number of doctors trained to treat the condition is also expected to contribute to market growth. North America, Europe and Asia are expected to be key markets.
Binge eating disorder may be seen in across all age groups, races, and income levels, however, it seems most prevalent among women. Among men, it is the most common eating disorder. Several companies are engaged in developing new treatments for the disorder. For example, in 2022, Tonix Pharmaceuticals Holding Corp. and Massachusetts General Hospital announced an agreement to assess TNX-1900 as a probable treatment for patients with binge eating disorder. The investigator-initiated phase 2 clinical trial, which was expected to launch in the second half of 2022, would be a randomized, double-blind, placebo-controlled study of 60 patients diagnosed with both binge eating disorder and obesity.
Vyvanse® (lisdexamfetamine dimesylate) is a central nervous system stimulant specified for the treatment of moderate to acute binge eating disorder and attention deficit hyperactivity disorder. Shire presented a supplemental new drug application for Vyvanse® for the treatment of moderate to severe binge eating disorder in adults to the FDA in July 2014. The drug received approval by the FDA for the indication in January 2015. Vyvanse® was also approved in Australia for both the conditions and in Canada, Europe, and Brazil for the treatment of ADHD. Vyvanse® is a key brand of Takeda under the neuroscience therapeutic area.
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In 2018, Chronos Therapeutics Ltd (Chronos) announced that the lead compound in its addiction programme, CT-010018 an orexin-1 antagonist, demonstrated positive pre-clinical proof of concept (POC) results in an in vivo model of binge eating disorder. Such developments are expected to boost the global binge eating disorder market. Orexin-1 antagonism was seen as an attractive target in binge eating disorder. Targeting this brain system had the promise to offer an effective treatment of binge eating disorder with no abuse liability, anhedonia, anorexia or somnolence.
In 2019, VIVUS announced the results of a clinical study (NCT02553824) demonstrating that patients with binge-eating disorder or bulimia nervosa receiving Qsymia (phentermine and topiramate extended-release (ER)) capsules CIV showed significant reduction in binge day frequency compared to placebo over four weeks. Also, Qsymia was well tolerated in these patient populations.
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