Implantica submits U.S. FDA Premarket Approval (PMA) application for RefluxStop® (first module)

An estimated 27% of the adult population in the U.S. struggle with GERD1 and 40% of GERD patients don't respond to PPIs, the most common medication to treat the disease.2 This leaves tens of millions of patients with limited options to treat the relentless, painful symptoms of GERD. Even worse, in the U.S. and EU, around 48,000 people die annually from esophageal adenocarcinoma, with strong indications in the literature to be caused by acid reflux. An estimated 27% of the adult population in the U...

An estimated 27% of the adult population in the U.S. struggle with GERD¹ and 40% of GERD patients don't respond to PPIs, the most common medication to treat the disease.² This leaves tens of millions of patients with limited options to treat the relentless, painful symptoms of GERD. Even worse, in the U.S. and EU, around 48,000 people die annually from esophageal adenocarcinoma, with strong indications in the literature to be caused by acid reflux.

Dr. Peter Forsell, CEO of Implantica, says, "This FDA filing is a key fundamental milestone for RefluxStop®³ and puts us in motion for the U.S. launch preparation ahead of the pending FDA approval. The basis for this expedited submission is the extraordinary 5-year clinical results from the RefluxStop CE mark study. Furthermore, more than 750 patients have been treated with the RefluxStop procedure in Europe, and the clinical outcome during the commercialization process has been in line with the CE study results."

Dr. Forsell continues, "The broader interest and acceptance for RefluxStop has been phenomenal so far and continues to grow rapidly among the leading European surgeons and Reflux centers of excellence, driven by exceptional patient outcomes and the larger medical community's support. With the recently announced completion of the US Human Factors study, a crucial milestone for PMA application, we are gearing up to file the next FDA module in three months time and are looking forward to bringing RefluxStop® to the U.S. market."

Reference:

For further information, please contact:
Nicole Pehrsson, Chief Corporate Affairs Officer
Telephone (CH): +41 (0)79 335 09 49
nicole.pehrsson@implantica.com

Implantica is listed on Nasdaq First North Premier Growth Market in Stockholm.

The company's Certified Adviser is FNCA Sweden AB, info@fnca.se

The information was sent for publication, through the agency of the contact person set out above, on March 27, 2024, at 08:00 a.m. (CET).

About Implantica
Implantica is a medtech group dedicated to bringing advanced technology into the body. Implantica's lead product, RefluxStop™, is a CE-marked implant for the prevention of gastroesophageal reflux that will potentially create a paradigm shift in anti-reflux treatment as supported by successful clinical trial results. Implantica also focuses on eHealth inside the body and has developed a broad, patent protected, product pipeline based partly on two platform technologies: an eHealth platform designed to monitor a broad range of health parameters, control treatment from inside the body and communicate to the caregiver on distance and a wireless energizing platform designed to power remote-controlled implants wirelessly through intact skin. Implantica is listed on Nasdaq First North Premier Growth Market (ticker: IMP A SDB). Visit www.implantica.com for further information.

About RefluxStop™
RefluxStop™ is a new innovative treatment that has the potential to spur a paradigm shift in anti-reflux surgery. It's unique mechanism of action differentiates it from standard of care and current surgical solutions. Longer established surgical options for GERD involve encircling the food passageway to support the lower esophageal sphincter's closing mechanism and are commonly associated with side effects such as swallowing difficulties, pain when swallowing and inability to belch and/or vomit.

In contrast, the RefluxStop device treats the cause of acid reflux without encircling and putting pressure on the food passageway. It restores and maintains the lower esophageal sphincter in its original, natural position.

The RefluxStop™ mechanism of action is focused on reconstructing all three components of the anti-reflux barrier, that if compromised could possibly result in acid reflux. It restores and supports the natural anatomical physiology of the body allowing the body to itself solve the problem with acid reflux.

Newsroom
https://www.implantica.com/media/media-kit

Community
https://ch.linkedin.com/company/implantica
https://www.twitter.com/implantica

Media Contact:
Implantica AG
Juanita Eberhart, VP Marketing & Advocacy
M: +1 925-381-4581
juanita.eberhart@implantica.com 

This information was brought to you by Cision http://news.cision.com

https://news.cision.com/implantica/r/implantica-submits-u-s--fda-premarket-approval--pma--application-for-refluxstop---first-module-,c3953137

The following files are available for download:

 

View original content:https://www.prnewswire.co.uk/news-releases/implantica-submits-us-fda-premarket-approval-pma-application-for-refluxstop-first-module-302100737.html