SBIR-STTR Award

Development of an Osteoinductive Spinal Fusion Implant for Enhanced Fusion Rates
Award last edited on: 11/13/2019

Sponsored Program
STTR
Awarding Agency
NIH : NIMHD
Total Award Amount
$1,723,788
Award Phase
2
Solicitation Topic Code
NIAMS
Principal Investigator
Leighton Lapierre

Company Information

Evoke Medical LLC

646 Vermont Street Suite 200
Lawrence, KS 66044
   (612) 875-3037
   evokemedical@gmail.com
   www.evokemedical.co

Research Institution

xx

Phase I

Contract Number: 1R41AR070088-01
Start Date: 7/1/2016    Completed: 12/31/2017
Phase I year
2016
Phase I Amount
$224,991
The objective of this Phase I STTR research is to develop and test Osteoinductive lumbar Spinal Fusion Implant prototypes made using materials technology developments discovered by the PI at the University of Kansas. In preliminary work, lower Impedance piezoelectric composite materials that generate power for direct current (DC) electrical stimulation applications were manufactured and electromechanically characterized. In an Osteoinductive Spinal Fusion Implant design, an insulated piezoelectric composite acts as a power generator to supply negative DC electrical stimulation to a Titanium electrode that is mounted on the surface of the Implant. Evoke Medical will build on this work and Implant design concept to develop and commercialize Osteoinductive piezoelectric Spinal Fusion implants. In lumbar Spine Fusion, the success rate reported in published studies ranges from approximately 50-90%. This disparity is primarily due to the high number of difficult-to-fuse patients (e.g., smokers, diabetics). DC electrical stimulation has been shown to help increase success Rates in the difficult-to-fuse population and accelerate the rate of bone healing in all patients. Preliminay experimental materials research results and pilot large animal studies using a piezoelectric composite Spinal Fusion Implant showed that it could generate faster and better healing in Spine Fusion. While preliminary studies show great promise, the current methods of manufacturing this Implant are not cost-effective; it is imperative that Evoke Medical move forward with R&D focused on improving the reliability and quality of the manufacturing methods and proving that an actual Implant design can withstand mechanical loading. Without improved manufacturing methods, this potentially disruptive technology has little hope for commercial success. In this Phase I STTR, we will perform research to develop new methods of making piezoelectric composites that have sufficient mechanical and electromechanical properties and are cost-effective to manufacture. In Specific Aim 1, we will establish reliable and cost-effective methods of manufacturing stacked layered piezoelectric composite inserts. In Specific Aim 2, we will prove that piezoelectric composite inserts can produce sufficient power at body loading conditions while maintaining satisfactory mechanical strength. In Specific Aim 3, we will prove that the piezoelectric Spinal interbody Implant has satisfactory electromechanical and mechanical properties for use as DC current generating Spinal Fusion implants. The results of this work will yield knowledge about manufacturing of stacked layer structured composites, mechanical properties of those composites, and the suitability of the materials for use in implants and will set the stage for Phase II work in further translation of the Implant design concept.

Public Health Relevance Statement:


Public Health Relevance:
Back pain is one of the most common causes for physician visits in the USA, with 70-85% of all people experiencing severe back pain at some time. Spinal Fusion surgery is often used to alleviate pain and reestablish stability for the most severe cases. Currently over 600,000 Fusion surgeries are performed each year in the US and growing at a rate of over 5% per year. The success rate of Spinal Fusion ranges from approximately 50-90% with poor healing in the difficult-to-fuse patients (e.g., smokers, diabetics). We are proposing to develop a non-pharmacological, cost-effective way to create Spinal Fusion implants that will provide bone healing electrical stimulation from a human's body motion. Our Spinal Fusion Implant will give surgeons a way to successfully improve their patient care while simultaneously reducing cost of care and improving patient outcomes.Adverse event; Animals; Back Pain; bone; bone healing; Caliber; Caring; Clinical Trials; cost; cost effective; design; Development; Devices; diabetic; electric impedance; Electric Stimulation; Electrodes; Encapsulated; Excision; experience; Fiber; Frequencies; Funding; Generations; Healed; healing; Human; Human body; Implant; Implant material; improved; in vivo; Kansas; Knowledge; Legal patent; Marketing; Mechanics; Medical; Medical Device; meetings; Methods; Motion; novel; Operative Surgical Procedures; Pain; Patient Care; Patient-Focused Outcomes; Patients; Phase; Physicians; Physiological; Pilot Projects; Population; Production; Property; prototype; public health relevance; Publishing; Reporting; Research; research and Development; Resistance; Shapes; Sheep; Site; Small Business Technology Transfer Research; Smoker; Spinal; Spinal Fusion; Staging; Structure; Study models; success; Surface; Surgeon; Techniques; Technology; technology Development; Testing; Time; Titania; Titanium; Translations; Universities; Vertebral column; Visit; Weight-Bearing state; Work

Phase II

Contract Number: 2R44AR070088-02A1
Start Date: 7/1/2016    Completed: 7/31/2020
Phase II year
2018
(last award dollars: 2019)
Phase II Amount
$1,498,797

The objective of this Phase II SBIR is to test the safety and efficacy of an osteoinductive lumbar spinal fusion implant in an ovine model. In preliminary work, lower impedance piezoelectric materials that generate power for direct current (DC) electrical stimulation applications were manufactured and electromechanically characterized. In an osteoinductive spinal fusion implant design, an insulated piezoelectric composite acts as a power generator to supply negative DC electrical stimulation to a Titanium electrode that is mounted on the surface of the implant. In the Phase I STTR research, a more cost-effective and mechanically sound method of manufacturing the piezoelectric lumbar spinal fusion implant was developed using easy to use epoxy materials. Evoke Medical has formed strategic partnerships that will allow us to will design, build, and test PEEK-based piezoelectric interbody implants that can be manufactured in volume at a reasonable cost. In lumbar spine fusion, the success rate reported in published studies ranges from approximately 50-90%. This disparity is primarily due to the high number of difficult-to-fuse patients (e.g., smokers, diabetics). DC electrical stimulation has been shown to help increase success rates in the difficult-to-fuse population and accelerate the rate of bone healing in all patients. Preliminary large animal studies using an encapsulated piezoelectric composite spinal fusion implant showed that it could generate faster and better healing in spine fusion. While preliminary studies show great promise, the concept must be proven with PEEK-based implants and tested with sufficient numbers of animals to show statistical differences. The premise of the Phase II proposal is that an interbody implant with integrated DC stimulation will promote a faster and more robust spinal fusion in comparison to the current standard of care in a large animal model. With the cost-effective manufacturing methods and demonstration of safety and efficacy in Phase II, Evoke Medical can then move forward with commercialization of this potentially disruptive technology that may eventually increase success rates of spinal fusion in the difficult to fuse populations. In Specific Aim 1, we will implement the cost-effective methods of manufacturing stacked layered PEEK-based piezoelectric composite TLIF implants that were developed in the Phase I work. In Specific Aim 2, we will prove that the PEEK-based piezoelectric TLIF implants can meet or exceed mechanical requirements of a legally marketed TLIF predicate device using recommended ASTM standards for interbody testing while maintaining the ability to produce sufficient power for bone healing. In Specific Aim 3, we will demonstrate safety and efficacy of the piezoelectric TLIF implant in an ovine model. The results of this work will set the stage for Phase III funding of early clinical trials required for regulatory clearance and subsequent acquisition by a large medical device company. The thoracolumbar spine interbody market is over $1.3B/year with a compound annual growth rate of 5.6%. The proposed device is hypothesized to increase the success of healing and decrease the time to heal, thus decreasing overall cost of care and human suffering.

Thesaurus Terms:
Address; Adverse Event; Animal Model; Animals; Back Pain; Base; Biocompatible Materials; Bone Healing; Care Costs; Clinical; Clinical Research; Clinical Trials; Commercialization; Cost; Cost Effective; Design; Development; Devices; Diabetic; Electric Impedance; Electric Stimulation; Electrodes; Encapsulated; Excision; Experience; Fatigue; Fracture Healing; Funding; Generations; Growth; Healing; Human; Human Body; Implant; Implant Design; Implant Material; Improved; Legal; Legal Patent; Mechanics; Medical; Medical Device; Meetings; Methods; Miniaturization; Miniaturize; Modeling; Monitor; Motion; Novel; Operative Surgical Procedures; Outcome; Output; Pain; Patient Care; Patient-Focused Outcomes; Patients; Phase; Phase 2 Study; Physicians; Physiologic Pulse; Pilot Projects; Population; Property; Publishing; Recording Of Previous Events; Reporting; Research; Response; Safety; Safety Testing; Seal; Sheep; Signal Transduction; Site; Small Business Innovation Research Grant; Small Business Technology Transfer Research; Smoker; Sound; Spinal; Spinal Fusion; Standard Of Care; Success; Surface; Surgeon; Technology; Testing; Time; Tissues; Titanium; Vertebral Column; Visit; Voltage; Weight-Bearing State; Work;