Actamax™ submits IDE to FDA for pivotal study on novel Sprayable Adhesion Barrier Device
"This IDE submission marks an important next step in advancing our Actamax Adhesion Barrier on the path to regulatory approval and commercialization," said Marc Hendriks, Ph.D., President of Actamax. "Previously obtained results from both the First-in-Human trial and the ensuing 12 months, long-term follow-up on the use of this adhesion barrier product are very promising. We believe that the data we are submitting to the FDA supports the safety and efficacy of the Actamax Adhesion Barrier. The proposed pivotal study in a larger population will help clarify the product’s place in the area of abdominopelvic surgery, where post-surgical adhesions are considered the most frequent complication.”
Surgery, trauma, infection and chronic inflammation (such as endometriosis) can elicit the formation of adhesions as part of the body’s normal healing response. Adhesions are excessive scar tissue that forms between adjacent internal tissues. A significant number of patients with adhesions develop complications ranging from discomfort, chronic pain and infertility (in women), to life-threatening consequences such as small bowel obstruction.
Previously, the safety, efficacy, and ease of use of the Actamax Adhesion Barrier was demonstrated in a 78-patient, multi-center clinical study in women undergoing a variety of gynecological surgeries. In the ensuing 12 month clinical follow-up of 47 study patients, there was evidence suggestive of improved long-term outcomes, including a lower recurrence rate of pre-study symptoms, and a higher probability of pregnancy in patients with whom the Actamax Adhesion Barrier was used.
Actamax Surgical Materials LLC is a DSM company. Actamax was founded in 2011 and is developing a new generation of resorbable, biocompatible surgical devices dedicated to improve patient outcomes and lives. For more information please visit www.actamax.com.