Business Wire09.04.18
Motus GI Holdings Inc., a medical technology company dedicated to improving endoscopy outcomes and experiences, announced that the Japanese Patent Office has issued a patent covering claims related to the company’s flagship product, the Pure-Vu System, a medical device that cleanses the colon intra-procedurally to facilitate improved visualization during a colonoscopy procedure to enable a quality exam and has demonstrated effective cleaning in hundreds of procedures.
“The need to improve the quality, efficiency and cost-effectiveness of inpatient colonoscopy procedures is a global issue. While our immediate focus continues to be on market development and preparation for commercial launch of the Pure-Vu System for inpatient colonoscopy in the U.S., we believe Japan is a key international market for future commercial expansion,” commented Mark Pomeranz, CEO of Motus GI. “Our goal is to make the Pure-Vu System the standard of care for inpatient colonoscopy procedures worldwide, and we are pleased to see our global IP portfolio continue to expand rapidly.”
Motus GI is currently focused on post-approval clinical trials and pilot commercial evaluations of the Pure-Vu System with leading U.S. hospitals in preparation for a commercial launch in the United States and select international markets in 2019 focused on the inpatient, hospital-based colonoscopy market where challenges with bowel prep slow diagnosis, diminish the quality of care, and add significant costs for hospitals.
Challenges with bowel preparation for inpatient colonoscopy represent a significant area of unmet need that directly affects clinical outcomes and the cost of care in a market that comprises nearly 4 million annual procedures worldwide. Published studies have found that the inpatient population has high rates of insufficiently prepped colons, which can lead to significantly longer hospital stays and other additional costs. This is exemplified in a recently published study from Northwestern University Hospital System which showed an average hospital stay extension of two days and cost increase of as much as $8,000 per patient as a result of challenges associated with bowel preparation. Motus GI believes that the Pure-Vu System may potentially reduce healthcare costs by reliably and predictably moving patients through the hospital system to a successful examination.
The Pure-Vu System is a 510(k) U.S. Food and Drug Administration-cleared medical device indicated to help facilitate the cleaning of a poorly prepared colon during the colonoscopy procedure. The device integrates with standard colonoscopes to enable cleaning during the procedure while preserving standard procedural workflow and techniques. The Pure-Vu System has received CE mark approval in Europe. The Pure-Vu System is currently being introduced on a pilot basis in the U.S. market, and the company is planning to initiate a full commercial launch focused on the inpatient colonoscopy market in the United States and select international markets in 2019.
“The need to improve the quality, efficiency and cost-effectiveness of inpatient colonoscopy procedures is a global issue. While our immediate focus continues to be on market development and preparation for commercial launch of the Pure-Vu System for inpatient colonoscopy in the U.S., we believe Japan is a key international market for future commercial expansion,” commented Mark Pomeranz, CEO of Motus GI. “Our goal is to make the Pure-Vu System the standard of care for inpatient colonoscopy procedures worldwide, and we are pleased to see our global IP portfolio continue to expand rapidly.”
Motus GI is currently focused on post-approval clinical trials and pilot commercial evaluations of the Pure-Vu System with leading U.S. hospitals in preparation for a commercial launch in the United States and select international markets in 2019 focused on the inpatient, hospital-based colonoscopy market where challenges with bowel prep slow diagnosis, diminish the quality of care, and add significant costs for hospitals.
Challenges with bowel preparation for inpatient colonoscopy represent a significant area of unmet need that directly affects clinical outcomes and the cost of care in a market that comprises nearly 4 million annual procedures worldwide. Published studies have found that the inpatient population has high rates of insufficiently prepped colons, which can lead to significantly longer hospital stays and other additional costs. This is exemplified in a recently published study from Northwestern University Hospital System which showed an average hospital stay extension of two days and cost increase of as much as $8,000 per patient as a result of challenges associated with bowel preparation. Motus GI believes that the Pure-Vu System may potentially reduce healthcare costs by reliably and predictably moving patients through the hospital system to a successful examination.
The Pure-Vu System is a 510(k) U.S. Food and Drug Administration-cleared medical device indicated to help facilitate the cleaning of a poorly prepared colon during the colonoscopy procedure. The device integrates with standard colonoscopes to enable cleaning during the procedure while preserving standard procedural workflow and techniques. The Pure-Vu System has received CE mark approval in Europe. The Pure-Vu System is currently being introduced on a pilot basis in the U.S. market, and the company is planning to initiate a full commercial launch focused on the inpatient colonoscopy market in the United States and select international markets in 2019.