DiscGenics Receives Approval from Japanese Pharmaceuticals and Medical Devices Agency to Begin Clinical Evaluation of Non-Surgical Degenerative Disc Disease Treatment in Japan
SALT LAKE CITY, /PRNewswire/ -- DiscGenics, Inc., a clinical stage biotechnology company focused on developing regenerative cell-based therapies that alleviate pain and restore function in patients with degenerative diseases of the spine, today announced the Japanese Pharmaceuticals and Medical Devices Agency (PMDA) has approved a Clinical Trial Notification (CTN) application for IDCT, an allogeneic injectable disc cell therapy for the treatment of degenerative disc disease (DDD).
IDCT is available off-the-shelf and offers a non-surgical therapeutic option for patients suffering from DDD. The CTN approval allows DiscGenics to advance IDCT into clinical studies in Japan.
DiscGenics intends to initiate a prospective, double-blinded, sham-controlled, multicenter clinical study to evaluate the safety and preliminary efficacy of IDCT in Japanese patients with painful, single-level lumbar DDD. The 38-patient trial is expected to begin enrolling in Japan in the first half of 2019.
"I am excited to be participating in the clinical evaluation of IDCT as a potential cell therapy to treat degenerative disc disease," said Dr. Daisuke Sakai, Associate Professor at the Department of Orthopaedic Surgery at the Tokai University School of Medicine in Kanagawa, and the study's principal investigator. "I recently participated in a preclinical study of IDCT's human Discogenic Cells in a canine disc degeneration model here in Japan, and was pleased to observe the cells' ability to stop disc height degeneration while improving the structure of the intervertebral disc. If similar results can be demonstrated in human subjects, the result could be reduced pain and disability associated with one of the most common causes of chronic low back pain."
Discogenic Cells are highly specialized progenitor cells that have been engineered from donated adult human intervertebral disc tissue, and are the therapeutic engine behind IDCT. A research article summarizing results from Dr. Sakai's study of Discogenic Cells in the canine disc degeneration model was recently published in the Journal of Orthopaedic Research Spine.
DDD is a painful, chronic and progressive disease that is characterized by inflammation and breakdown of extracellular matrix within the intervertebral disc. The condition is estimated to affect more than one million people, including 200,000 patients needing surgical intervention every year in Japan. Current treatment options for DDD are limited to physical rehabilitation programs and pain management, including opioids, in the earlier stages. In the more advanced stages, oftentimes a patient's only option is surgical intervention to remove the painful disc(s), fuse two or more vertebral bones together and/or replace bone or tissue altogether. However, back surgeries often have limited success and may result in subsequent adjacent level degeneration.
DiscGenics is leveraging the accelerated regenerative medicine pathway created by the Japanese Pharmaceuticals and Medical Devices Act (a revision of the Pharmaceutical Affairs Act) to pursue regulatory approval of IDCT in Japan, and has been working closely with the PMDA through a series of consultations to satisfy all requirements for trial design and materials safety.
"We are thrilled to have received the go-ahead from the PMDA to begin clinical study of IDCT in Japan," said Flagg Flanagan, Chief Executive Officer and Chairman of the Board of Directors for DiscGenics. "DDD is a debilitating condition and we believe IDCT has the potential to offer a revolutionary and possibly curative solution for the millions who suffer from it. Importantly, Japan represents the third largest healthcare market in the world, affording DiscGenics the potential opportunity to help many, many people who are currently enduring chronic low back pain with no end in sight."
DiscGenics is also conducting an ongoing Phase I/II prospective, randomized double-blinded, vehicle- and placebo-controlled, multicenter clinical study of IDCT in the U.S. among subjects with single-level, symptomatic lumbar DDD. Through this study, IDCT is being evaluated under an investigational new drug (IND) allowance by the U.S. Food and Drug Administration (FDA) and will be regulated as a drug-biologic through a therapeutics biologics application (BLA).
View original content to download multimedia:http://www.prnewswire.com/news-releases/discgenics-receives-approval-from-japanese-pharmaceuticals-and-medical-devices-agency-to-begin-clinical-evaluation-of-non-surgical-degenerative-disc-disease-treatment-in-japan-300763083.html
SOURCE DiscGenics, Inc.