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Article in IA Journal: Issue 233 Autumn 2016

OstomyCure AS has been published in The Ileostomy & Internal Pouch Support Groups latest issue of the IA Journal.

Download the article below or visit www.iasupport.org

Large clinical study started in UK and Sweden

2018-05-29

Approval for multicenter study “TIES-C03” in major university hospitals in Leeds, UK & Umeå, Sweden. OstomyCure AS has achieved an important milestone on the way to making the revolutionary TIES® Solution available to ileostomy patients, a patient population that has not experienced any meaningful improvements in “standard of care” in the last 30-40 years. The study aims to gather more and longer term clinical data regarding safety, performance and Quality of Life. The study has started at Norrland University Hospital, Umeå, Sweden with Associate Professor Karin Strigård and Prof. Ulf Gunnarsson and at St. James Hospital, Leeds with Professor David Jayne as the main investigators. OstomyCure plans to commit additional clinical centers (primarily in the UK) to participate in the “TIES-C03” study.

Latest update on TIES Solution

2018-01-11

Message from CEO Ostomycure Dr Benedict Broenniman M.D.

OstomyCure AS Appoints new Chief Medical Officer

2017-01-31

OstomyCure today announced the appointment of Cindy Wong, M.D. as Chief Medical Officer (CMO).

Experienced Chief Commercial Officer Joins OstomyCure AS

2016-09-26

OstomyCure AS engages Morten Gunvad, currently founder and Head of GP Consulting GmbH, as Chief Commercial Officer of the TIES® System.

The TIES® System represented at major political event

2016-06-29

The TIES® Implant and Lid will be represented at Almedalsveckan, an annual political event taking place in Visby, Sweden.

Significant Breakthrough for Stoma Patients

2016-06-20

Aimed to dramatically improve the patient’s quality of life, the TIES® System, a new concept in continent ileostomy receives CE marking.

CE-marking for the TIES® System

2016-06-10

Today, OstomyCure is very pleased to announce that the TIES® System has received approval for CE marking from our Notified Body.

Technical File submitted for CE approval of TIES®

2016-03-24

Comprising an implantable medical device, the TIES® System requires approval from a Notified Body in order to obtain CE marking and to be marketed in Europe.

TIES® clinical study fully enrolled

2015-11-16

The ongoing TIES® clinical study is moving forward and is now fully enrolled with the planned number of patients.