Zoek in het archief
 
terug

Check the original
News breaking: 2017-11-07

Axonics® krijgt IDE-status van Amerikaanse FDA voor cruciaal onderzoek naar sacrale zenuwstimulatie tegen problemen aan urinewegen

IRVINE, Calif.–(BUSINESS WIRE)– Axonics Modulation Technologies, Inc., ontwikkelaar van het eerste oplaadbare systeem voor sacrale zenuwstimulatie voor de behandeling van functiestoornissen aan de blaas of darmen, heeft vandaag bekendgemaakt dat de Amerikaanse Food & Drug Administration (FDA) het bedrijf een Investigational Device Exemption (IDE) heeft toegewezen in overeenstemming met de regulering 21 CFR 812. Dit stelt Axonics in staat een cruciaal onderzoek uit te voeren, waarmee het een goedkeuring van FDA in de Verenigde Staten kan verkrijgen.

“De FDA voerde in 2017 een belangrijk onderzoek uit in het kader van het IDE-proces. De focus van het technische onderzoek lag bij veiligheid op de lange termijn van het implantaat. Het feit dat we onze claim over een vijftienjarige levensduur als implantaat konden onderbouwen met robuuste design- en ontwikkelingsprocessen, risicoanalyse en uitgebreide tests, bewijst de hoge kwaliteit van ons team”, zei Raymond W. Cohen, CEO van Axonics. “Gezien de vraag in de Verenigde Staten naar sacrale zenuwstimulatie, is goedkeuring door de FDA onze belangrijkste focus. Met dat doel voor ogen zijn we erop gebrand dit goed opgezette onderzoek snel uit te voeren in het belang van patiënten.”

Axonics® Receives IDE Clearance from U.S. FDA to Conduct a Pivotal Study with its Sacral Neuromodulation System for the Treatment of Urinary Dysfunction

IRVINE, Calif.–(BUSINESS WIRE)– Axonics Modulation Technologies, Inc., developer of the first rechargeable sacral neuromodulation (r-SNM™) system for the treatment of overactive bladder (OAB) and bowel dysfunction, today announced the U.S. Food & Drug Administration (FDA) has granted an Investigational Device Exemption (IDE) in accordance with 21 CFR 812 regulations allowing Axonics to conduct a pivotal study designed to gain FDA approval in the United States.

“During 2017, as part of the IDE process, the FDA conducted a significant review of our product. A major focus of the technical review was the long-term safety of our implant. The fact that we were able to support our anticipated 15-year full system life-in-the-body claim based on our robust design and development processes, risk analysis and extensive validation testing is testament to the high-quality work of our team,” said Raymond W. Cohen, Chief Executive Officer of Axonics. “Given the demand in the U.S. market for SNM therapy, gaining FDA approval is our main focus. To that end, we fully intend to execute this well-designed pivotal study with velocity and in the best interests of patients.”

Axonics expects to begin enrolling patients in the clinical study (ARTISAN-SNM) in November 2017, with a target of approximately 120 patients to be implanted at 15 centers of excellence located in the U.S. and Western Europe.

The ARTISAN-SNM study is a single-arm, prospective pivotal study designed to demonstrate the safety and effectiveness of the Axonics r-SNM system as an aid in the treatment of urinary urgency incontinence in patients who have failed or could not tolerate more conservative treatments.

Karen L. Noblett, M.D., Axonics Chief Medical Officer, stated, “The endpoints of the ARTISAN-SNM pivotal study are comparable to published clinical literature for urinary dysfunction. We will be analyzing, among other things, the proportion of responders to SNM therapy at six months post-implant based on reduction in urinary urgency incontinence episodes from the patient’s baseline diary. There has been an overwhelming response from the Urology and Urogynecology community to be part of this pivotal study and, as a result, we have some of the most experienced and prolific implanters as study investigators.”

During 2016, the Axonics r-SNM system gained regulatory approval in Europe and Canada for the treatment of overactive bladder, urinary urgency incontinence, urinary retention and fecal incontinence.

About Axonics Modulation Technologies, Inc.

Axonics, based in Irvine, CA, is a privately-held venture backed company that has developed a novel implantable neuromodulation technology for patients with urinary and bowel dysfunction. The Axonics r-SNM system includes a miniaturized rechargeable implantable neurostimulator qualified to function at least 15 years in the body, a charging system optimized for reduced charge time with no heating, a patient-friendly remote control and an intuitive clinician programmer that facilitates the lead placement procedure and programming. For more information, visit the Company’s website at www.axonicsmodulation.com.

View source version on businesswire.com: http://www.businesswire.com/news/home/20171106006189/en/

Contacts

Axonics Modulation Technologies, Inc.

Dan Dearen, +1-949-396-6322

Chief Operating & Financial Officer

ddearen@axonicsmodulation.com

or

Pure Communications, Inc.

Matt Clawson, +1-949-370-8500

mclawson@purecommunications.com

Deze bekendmaking is officieel geldend in de originele brontaal. Vertalingen zijn slechts als leeshulp bedoeld en moeten worden vergeleken met de tekst in de brontaal, die als enige rechtsgeldig is.