Country for PR: United States
Contributor: PR Newswire New York
Tuesday, August 27 2019 - 09:00
AsiaNet
DiscGenics Receives FDA Fast Track Designation for Cell Therapy for Disc Degeneration
SALT LAKE CITY, Aug. 27, 2019 /PRNewswire-AsiaNet/ --

DiscGenics, Inc. ( https://www.discgenics.com/ ), 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 that the U.S. Food and Drug Administration (FDA) 
has granted Fast Track designation for its investigational cell therapy, IDCT, 
currently being evaluated in regulator-allowed clinical trials in the U.S. and 
Japan for the reduction in pain and disability associated with degenerative 
disc disease (DDD), a major cause of chronic low back pain. 

Video - https://www.youtube.com/watch?v=KEpAB23EbOI  
Logo - https://mma.prnewswire.com/media/561675/DiscGenics_Logo.jpg 

Fast Track ( 
https://c212.net/c/link/?t=0&l=en&o=2560933-1&h=1344265282&u=https%3A%2F%2Fwww.fda.gov%2Fpatients%2Ffast-track-breakthrough-therapy-accelerated-approval-priority-review%2Ffast-track&a=Fast+Track 
) is a special regulatory designation that companies can apply for once they 
have sufficient preclinical and clinical evidence that a product may be able to 
treat an unmet medical need for a serious medical condition. With this 
designation, Sponsors may benefit from early and frequent communication with 
FDA, eligibility for Accelerated Approval and Priority Review programs, as well 
as a Rolling Review application process for marketing licensure. 

"We are thrilled to receive Fast Track designation for IDCT as it recognizes 
the extremely compelling preclinical ( 
https://c212.net/c/link/?t=0&l=en&o=2560933-1&h=3096744115&u=https%3A%2F%2Fwww.thespinejournalonline.com%2Farticle%2FS1529-9430(19)30935-0%2Ffulltext&a=preclinical 
) (1) and safety data ( 
https://c212.net/c/link/?t=0&l=en&o=2560933-1&h=791438136&u=https%3A%2F%2Fwww.discgenics.com%2Fnews-posts%2F2019%2F1%2F7%2Fdiscgenics-announces-that-idct-has-passed-the-initial-safety-review-of-its-first-in-human-clinical-trial-for-degenerative-disc-disease&a=safety+data 
) we have generated for IDCT through our robust research and development and 
clinical programs, and underscores FDA's acknowledgement of low back pain as a 
serious medical condition with a profound lack of treatment options," said 
Flagg Flanagan, Chairman and CEO of DiscGenics, Inc. "This Fast Track 
designation reinforces our commitment to working with regulators to identify 
ways to accelerate development and expedite approval of the therapy within 
existing regulatory frameworks to make IDCT available to patients as quickly as 
possible."

IDCT is a homologous, allogeneic, injectable cell therapy that utilizes 
biomedically engineered progenitor cells, known as Discogenic Cells ( 
https://c212.net/c/link/?t=0&l=en&o=2560933-1&h=2823742337&u=https%3A%2F%2Fwww.discgenics.com%2Fresearch-and-development%2F&a=Discogenic+Cells 
), that have been derived from intervertebral disc tissue to offer a 
non-invasive, potentially regenerative solution for the treatment of mild to 
moderate DDD. As a manufactured allogeneic cell therapy, IDCT is regulated by 
FDA's Center for Biologics Evaluation and Research (CBER) under Section 351 of 
the Public Health Service Act (PHSA). As a result, DiscGenics is adhering to 
the rigors of a regulated drug pathway that require the Company to not only 
prove that the product has a therapeutic effect through clinical evaluation, 
but also that it meets critical safety standards and is produced consistently 
from lot to lot through adherence to current good manufacturing practice (cGMP) 
standards for a cell therapy. 

DiscGenics is conducting two parallel prospective, randomized, double-blinded, 
controlled, multicenter clinical trials of IDCT in the U.S. ( 
https://c212.net/c/link/?t=0&l=en&o=2560933-1&h=737266639&u=https%3A%2F%2Fclinicaltrials.gov%2Fct2%2Fshow%2FNCT03347708&a=U.S. 
) and Japan ( 
https://c212.net/c/link/?t=0&l=en&o=2560933-1&h=1164363533&u=https%3A%2F%2Fclinicaltrials.gov%2Fct2%2Fshow%2FNCT03955315&a=Japan 
). IDCT is being evaluated in the U.S. under an investigational new drug (IND) 
allowance by the FDA and will be regulated as a drug-biologic through a 
biologics license application (BLA). In Japan, the trial ( 
https://c212.net/c/link/?t=0&l=en&o=2560933-1&h=3128444002&u=https%3A%2F%2Fwww.discgenics.com%2Fnews-posts%2F2019%2F8%2F7%2Fdiscgenics-announces-first-patients-treated-in-japanese-clinical-trial-of-cell-therapy-for-degenerative-disc-disease&a=trial 
) is supported by a Clinical Trial Notification (CTN) approved by the Japanese 
Pharmaceuticals and Medical Devices Agency (PMDA). Primary outcome measures 
include safety and reduction in pain. Secondary outcome measures include 
reduction in disability and radiographic improvement. Importantly, the U.S. 
study has shown safety in the first cohort of patients ( 
https://c212.net/c/link/?t=0&l=en&o=2560933-1&h=2622105774&u=https%3A%2F%2Fwww.discgenics.com%2Fnews-posts%2F2019%2F1%2F7%2Fdiscgenics-announces-that-idct-has-passed-the-initial-safety-review-of-its-first-in-human-clinical-trial-for-degenerative-disc-disease&a=shown+safety+in+the+first+cohort+of+patients 
). For both studies, enrollment is ongoing. 

About Chronic Low Back Pain and Degenerative Disc Disease 
Chronic low back pain is a serious medical condition that represents a leading 
cause of disability worldwide (2) and is the most common non-cancer reason for 
opioid prescription in the U.S. (3). It affects 12-30% of U.S. adults at a 
given time (4) and is estimated to cost the U.S. healthcare system over $100 
billion each year (2), creating a significant burden on the economy and 
individual patients dealing with the condition. In nearly 40% of patients, low 
back pain is caused by DDD (5-7), a chronic and progressive condition where the 
intervertebral disc breaks down and causes pain.

About DiscGenics 
DiscGenics is a privately held, 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. As the only 
company in the world to develop an allogeneic cell therapy derived from 
intervertebral disc cells to treat diseases of the disc, DiscGenics believes it 
has a unique opportunity to harness the restorative potential of the human body 
to heal millions of patients suffering from the debilitating effects of back 
pain. DiscGenics' first product candidate, IDCT, is a homologous, allogeneic, 
injectable cell therapy that utilizes biomedically engineered progenitor cells 
derived from intervertebral disc tissue, known as Discogenic Cells, to offer a 
non-surgical, potentially regenerative solution for the treatment of patients 
with mild to moderate degenerative disc disease. For more, visit 
www.discgenics.com. 

References 

1. Silverman, L., Dulatova, G., Tandeski, T., Erickson, I., Lundell, B., 
Toplon, D., Wolff, T., Howard, A., Chintalacharuvu, S., Foley, K. In Vitro and 
In Vivo Evaluation of Discogenic Cells, An Investigational Cell Therapy for 
Disc Degeneration. The Spine Journal, published online 2019 Aug 20. 

2. Hoy, D., March, L., Brooks, P., Blyth, F., Woolf, A., Bain, C., Williams, 
G., Smith, E., Vos, T., Barendregt, J., Murray, C., Burstein, R., and 
Buchbinder, R. The global burden of low back pain: estimates from the Global 
Burden of Disease 2010 study. Ann Rheum Dis 73, 968, 2014. 

3. Ringwalt, C., Gugelmann, H., Garrettson, M., Dasgupta, N., Chung, A.E., 
Proescholdbell, S.K., and Skinner, A.C. Differential prescribing of opioid 
analgesics according to physician specialty for Medicaid patients with chronic 
noncancer pain diagnoses. Pain Res Manag 19, 179, 2014. 

4. Davis, M.A., Onega, T., Weeks, W.B., and Lurie, J.D. Where the United States 
spends its spine dollars: expenditures on different ambulatory services for the 
management of back and neck conditions. Spine (Phila Pa 1976) 37, 1693, 2012. 

5. Freemont, A.J. The cellular pathobiology of the degenerate intervertebral 
disc and discogenic back pain. Rheumatology (Oxford) 48, 5, 2009. 

6. Anderson, D.G., and Tannoury, C. Molecular pathogenic factors in symptomatic 
disc degeneration. Spine J 5, 260S, 2005. 

7. Zhang, Y.G., Guo, T.M., Guo, X., and Wu, S.X. Clinical diagnosis for 
discogenic low back pain. Int J Biol Sci 5, 647, 2009.

Media Contact 
Lindsey Saxon 
lindsey@discgenics.com 

SOURCE  DiscGenics, Inc.

CONTACT: Lindsey Saxon, (206) 335-0114
Translations

Japanese