Country for PR: United States
Contributor: PR Newswire New York
Friday, October 28 2022 - 12:30
AsiaNet
Sebela Pharmaceuticals(R) Acquires Exclusive Licensing Rights to Develop and Commercialize Tegoprazan in the U.S. and Canada
BRAINTREE, Mass., Oct. 28, 2022 /PRNewswire-AsiaNet/ --

  -- Phase 3 Trials Initiated with Tegoprazan for the Treatment of 
     Erosive Esophagitis and Non-erosive Reflux Disease

Sebela Pharmaceuticals(R) has entered an exclusive partnership with HK inno.N 
Corporation to license tegoprazan in the United States and Canada. Under the 
agreement, Braintree Laboratories, a leader in gastroenterology and an 
affiliate of Sebela Pharmaceuticals, will be responsible for clinical 
development, registration, marketing, and sales in the United States and 
Canada. Tegoprazan, a novel potassium-competitive acid-blocker (P-CAB), is 
currently approved and marketed in several territories, including South Korea 
and China. 

Photo - https://mma.prnewswire.com/media/1929505/Sebela_Pharmaceuticals.jpg

"We are delighted to add tegoprazan to our product pipeline," said Alan Cooke, 
President and CEO of Sebela Pharmaceuticals. "For over 35 years we have been 
committed to the gastroenterology space and to those affected by GI diseases. 
Tegoprazan expands our gastroenterology portfolio into an exciting new 
therapeutic class. Tegoprazan already has an established track record of safety 
and efficacy in multiple clinical studies and represents a potential new 
treatment option for people living with GERD."

"We are delighted to partner with Sebela Pharmaceuticals," Dal-Won Kwak, CEO, 
HK inno.N said in a statement. "Sebela has vast development, regulatory and 
commercial experience and expertise in the US, having obtained FDA approval and 
successfully launched multiple gastroenterology products over more than three 
decades. We believe Sebela Pharmaceuticals is the ideal partner to develop and 
commercialize tegoprazan in the United States and Canada." 

Following successful discussions with the US Food and Drug Administration, 
Sebela Pharmaceuticals has initiated Phase 3 studies of tegoprazan in patients 
with gastroesophageal reflux disease (GERD). The Phase 3 GERD program, known as 
the TRIUMpH program, includes a large, multi-center, double-blind study 
evaluating the safety and efficacy of tegoprazan versus a PPI control for the 
indications of healing of all grades of erosive esophagitis (EE) and the 
maintenance of EE healing and relief of heartburn. The TRIUMpH program also 
includes a large, multicenter, double-blind, placebo-controlled study designed 
to demonstrate the safety and efficacy of tegoprazan in patients with 
non-erosive reflux disease (NERD).  

About Tegoprazan

Tegoprazan is a novel agent in development for the treatment of acid-related 
gastrointestinal diseases. It is a member of a class of oral medications known 
as P-CABs, or potassium-competitive acid blockers, which have been shown to 
have rapid onset of action and the ability to control gastric pH for longer 
periods of time than proton pump inhibitors (PPIs). Tegoprazan has already 
received marketing authorization in multiple territories, including South Korea 
and China.

About GERD

GERD is a chronic and highly prevalent disorder caused by repeated backflow (or 
reflux) of gastric contents into the esophagus. GERD is characterized by a wide 
variety of symptoms, including heartburn and acid regurgitation. The main 
phenotypic presentations of GERD include non-erosive reflux disease (NERD) and 
erosive esophagitis (EE). EE is usually clinically differentiated from NERD by 
the presence of mucosal inflammation and lesions in the distal esophagus. 
Poorly treated EE can lead to Barrett's esophagus which increases the risk of 
esophageal cancer. It is estimated that GERD affects approximately 65 million 
people in the US with 60% to 70% suffering from NERD. While proton pump 
inhibitors are the mainstay of therapy for both EE and NERD, 35% to 54% of 
patients fail to achieve complete relief of symptoms. This represents a large 
unmet and underappreciated patient need. 

About Sebela Pharmaceuticals(R) 

Sebela Pharmaceuticals is a US pharmaceutical company with a market leading 
position in gastroenterology and a focus on innovation in women's health.  
Braintree, a part of Sebela Pharmaceuticals, is the market leader in 
colonoscopy screening for over 35 years, having invented, developed and 
commercialized a broad portfolio of innovative prescription colonoscopy 
preparations and multiple gastroenterology products.  Braintree also has 
multiple gastroenterology programs in late-stage clinical development.  In 
addition, Sebela Women's Health has two next generation intra-uterine devices 
(IUDs) for contraception in the final stages of clinical development. Sebela 
Pharmaceuticals has offices/operations in Roswell, GA; Braintree, MA; and 
Dublin, Ireland; has annual net sales of approximately $200 million; and has 
grown to over 320 employees through strategic acquisitions and organic growth.

Please visit sebelapharma.com ( 
https://c212.net/c/link/?t=0&l=en&o=3683008-3&h=3526104333&u=https%3A%2F%2Fsebelapharma.com&a=sebelapharma.com 
) for more information or call 800-874-6756. 

About HK inno.N Corporation

HK inno.N is a public South Korean pharmaceutical company that develops, 
manufactures, and commercializes pharmaceuticals for both the domestic and 
international markets. HK inno.N's key businesses are in the areas of 
prescription drugs, health supplements and beauty products. Since its 
establishment in 1984, through exports and global alliances, the company is 
growing into an international pharmaceutical firm. Drawing on the company's 
experience and knowhow in developing novel drugs, HK inno.N succeeded in 
launching new GERD treatment 'K-CAB(R)" (Tegoprazan), the 30th novel drug to be 
developed and registered in Korea, to great acclaim. For more information, 
visit https://www.innon.com/eng.

Source - Sebela Pharmaceuticals

CONTACT: Jeanine Kober, Red Havas, E: jeanine.kober@redhavas.com, P: 
646-418-5241

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