SBIR-STTR Award

Preclinical Evaluation of a Biofabricated Implant for Rotator Cuff Tendon-Enthesis Regeneration
Award last edited on: 1/22/20

Sponsored Program
SBIR
Awarding Agency
NIH : NIAMS
Total Award Amount
$223,907
Award Phase
1
Solicitation Topic Code
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Principal Investigator
Michael Paul Francis

Company Information

Embody Inc

4112 Monarch Way Suite 409
Norfolk, VA 23508
   (757) 777-5674
   N/A
   embody-inc.com
Location: Single
Congr. District: 03
County: Norfolk city

Phase I

Contract Number: 1R43AR076841-01
Start Date: 9/19/19    Completed: 3/31/20
Phase I year
2019
Phase I Amount
$223,907
Rotator cuff injuries are a major clinical problem, leading to 250,000 surgical rotator cuff repair (RCR) procedures performed annually in the U.S. alone. Re-rupture rates following RCR are reported upwards of 95% with the current standard of care. Addressing the clinical need for improving rotator cuff healing, the goals of this research are to optimize the biomanufacturing, preservation and in vivo performance of a Biologically-enhanced Tissue ENgineered Device (Bio-TEND) for tendon and tendon-to-bone (enthesis) regeneration. Supported by multiple patents, Bio-TEND is: 1.) a well- characterized, anisotropic, resorbable collagen microfibrous graft electrospun from a benign solvent; 2.) engineered for high void to promote rapid cellular ingrowth and remodeling; and 3.) biomanufactured with clinical grade stem cells primed for tendon and fibrocartilage formation to promote enthesis regeneration. Our hypothesis is that Bio-TEND grafts will accelerate the production of new, host-generated, dense, regularly oriented tendon-like tissue and enthesis integration in a RCR model. We will accomplish two specific aims necessary for progressing through FDA approval and to commercialization. Aim 1: Establish Optimal Bio-TEND Biomanufacturing and Preservation Strategies. Aim 2: Assess Bio-TEND in a Chronic Rat RCR Model. Successful completion of our SBIR Phase I work will yield biomanufacturing of a therapeutic for RCR, including scale up, preservation and performance studies. This work will lead to pivotal testing in large animals and Mechanism of Action studies in SBIR Phase II, and human clinical trials in Phase III. Results of these SBIR studies will provide the data required for FDA submission and to successfully market the product. This project brings together investigators with the necessary complementary expertise in the translation of medical devices and cellular therapies (Dr. Francis, Embody), and tendon biology, biomechanics and animal models for RCR (Dr. Soslowsky, Penn), working together with world-class surgeons to develop this critical therapeutic.

Public Health Relevance Statement:
Preclinical Evaluation of a Biofabricated Implant for Rotator Cuff Tendon- Enthesis Regeneration Project Narrative This work will develop an advanced biomanufactured graft to significantly improve rotator cuff healing for the 250,000 patients with surgical rotator cuff repair annually in the U.S., which is critically needed in light of the upwards of 95% re-rupture rates reported. The goals of this research are to optimize the biomanufacturing, preservation and performance of a Biologically-enhanced Tissue ENgineered Device (Bio-TEND) for tendon and tendon-to-bone (enthesis) regeneration, and to evaluate putative mechanisms of action (MOA) and therapeutic potential in vivo. Our hypothesis is that Bio-TEND grafts will accelerate the production of new, host- generated, dense, regularly oriented tendon-like tissue and enthesis integration in a rotator cuff repair model.

Project Terms:
Address; Air; Animal Model; Animals; base; Benign; Biocompatible Materials; Biological; Biology; Biomanufacturing; biomechanical model; Biomechanics; BMP-12; bone; Bone Marrow; Cadaver; Cells; Chronic; Clinical; clinical translation; Clinical Trials; Collagen; commercialization; Cryopreservation; Cyclic GMP; Data; Defect; Dermis; design; Development; Devices; dosage; Engineering; Evaluation; Fibrocartilages; Goals; healing; Health; Histology; Human; Implant; implantation; improved; in vivo; in vivo evaluation; innovation; Legal patent; Letters; Light; Mechanics; Medical Device; meetings; Mesenchymal Stem Cells; Metabolic; Methodology; Modeling; Musculoskeletal; Natural regeneration; novel; off-patent; Operative Surgical Procedures; Outcome; Patients; Performance; Phase; Polarization Microscopy; Polymers; Population; preclinical evaluation; preclinical study; preservation; Procedures; Production; Rattus; regenerative; Regenerative Medicine; relative effectiveness; repaired; Reporting; Research; research and development; Research Personnel; Rotator Cuff; rotator cuff injury; Route; Rupture; scale up; Shoulder; Small Business Innovation Research Grant; Solvents; Source; standard of care; Stem cells; Surgeon; Technology; Tendon structure; Testing; Therapeutic; Tissue Engineering; tissue regeneration; Tissues; Translations; Tube; Work

Phase II

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
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Phase II Amount
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