Relievant Medsystems, Inc. Receives FDA 510(k) Clearance for INTRACEPTŪ for the Relief of Chronic Low Back Pain

Thursday, July 21, 2016 General News J E 4
Landmark Level 1 Clinical Study Provides Compelling Data for New Therapy

REDWOOD CITY, Calif., July 21, 2016 /PRNewswire/ -- Relievant Medsystems, Inc., a privately held medical device company pioneering the therapy of nerve ablation within vertebral bodies for the treatment of chronic low back pain, announced today that it received U.S. Food and Drug Administration (FDA) 510(k) clearance for the INTRACEPTŪ Intraosseous Nerve Ablation System.

The INTRACEPT System is the first specific therapy to relieve chronic low back pain (CLBP) of at least six months duration that has not responded to at least six months of conservative care caused by changes associated with degeneration of spinal vertebral bodies and the associated intervertebral discs.

The INTRACEPT System uses radio frequency (RF) energy, delivered through specially designed instruments via a minimally invasive approach to access and ablate the basivertebral nerve (BVN.) The BVN is a sensory nerve within each vertebral body, which transmits the sharp, aching or throbbing pain experienced with degenerated vertebral bodies. Spine specialists can use the INTRACEPT System to treat one or more levels between L3 and S1 in the lower spine.

The FDA clearance followed the Agency's review of the Company's landmark SMART (Surgical Multi-Center Assessment of RF Ablation for the Treatment of Vertebrogenic Back Pain) study, a 225-patient, Level 1, international, prospective, randomized, double-blind, sham-controlled clinical trial, that evaluated the safety and effectiveness of the INTRACEPT therapy for the treatment of chronic low back pain. Patients were followed at two and six weeks, and at three, six, 12 and 24 months.  Endpoints included Oswestry Disability Index (ODI), a validated assessment that measures a patient's disability due to their back pain. 

Key findings from the Level 1 SMART study include:

  • For patients who successfully received the intended therapy and completed the follow-up, results of the primary endpoint analysis for this per protocol population at 3-months showed that the mean ODI improvement observed in the INTRACEPT treatment arm was statistically superior to the sham arm (p = 0.019).
  • In these patients, the INTRACEPT treatment arm demonstrated a mean ODI improvement of 20.5 points or 48% decrease from baseline at 3 months.
  • In this same patient population, greater than 75% of patients treated with INTRACEPT demonstrated an ODI improvement equal to or greater than 10 points, the minimally clinically important difference (MCID) threshold.
  • Results in the INTRACEPT treatment arm were sustained through 12 and 24 months of follow-up.

"Chronic low back pain is one of the most prevalent and expensive medical problems in the United States and worldwide," said Alex DiNello, President and CEO of Relievant Medsystems. "Relievant's minimally invasive INTRACEPT System is intended to fill the large therapeutic gap that currently exists between conservative treatments, such as physical therapy or narcotics, and highly invasive surgical interventions such as spinal fusion surgery."

Jeffrey Fischgrund, MD, principal investigator of the SMART study and Professor and Chairman of the Department of Orthopaedic Surgery at Beaumont Health System in Royal Oak, Michigan stated, "We see patients every day with greater than six months of chronic low back pain that is not responsive to conservative care. INTRACEPT, as demonstrated in the rigorously designed and executed SMART trial, is an important breakthrough therapy with clinically meaningful results for patients and has an excellent safety profile."

"We are pleased to receive the FDA's 510(k) clearance and to see the excellent clinical outcomes obtained from the robust SMART study," Richard Mott, Relievant's Executive Chairman of the Board of Directors stated. "They are important milestones for the Company, and we look forward to bringing this new therapeutic option to clinicians to enable them to treat their patients who suffer from chronic low back pain."

About Chronic Low Back Pain CLBP affects nearly one-third of the U.S. population and represents the largest and most expensive non-lethal condition in the healthcare system. Every year, approximately 12 million new patients seek treatment for back pain. Unfortunately, nearly two million of these patients fail to respond to conservative therapies and face limited options, including escalating use of narcotic pain medications, invasive surgical procedures (including spinal fusion) or continued suffering.

About INTRACEPT and Basivertebral Nerve (BVN) Ablation The INTRACEPT Intraosseous Nerve Ablation System is a patent-protected, minimally invasive, implant-free therapy that utilizes radiofrequency energy delivered into the vertebral body of the spine to ablate the BVN. This nerve, characterized in peer-reviewed literature reporting studies of pain signal transmission and in preclinical and clinical evaluations, is a significant contributor in the transduction of pain arising from degeneration of the vertebral bodies associated with CLBP. The INTRACEPT Intraosseous Nerve Ablation System leverages proprietary instruments and methods to disable this nerve.

Important Safety Information

The INTRACEPT Procedure, as with any surgical procedures, has risks that should be discussed with your medical professional.

About Relievant Medsystems Relievant Medsystems, Inc. is a privately held medical device company based in Redwood City, California. The Company's investors include Canaan Partners, Emergent Ventures, Morgenthaler Ventures, New Enterprise Associates and ONSET Ventures.

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SOURCE Relievant Medsystems, Inc.



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