Medical Device News Magazine

Frank Vizesi Appointed Chief Scientific Officer at Theradaptive | Strengthens Executive Team

About Medical Device News Magazine

About Medical Device News Magazine. We are a digital publication founded in 2008 located in the United States.

Advertise with Medical Device News Magazine! Join Our #1 Family of Advertisers!

We pride ourselves on being the best-kept secret when it comes to distributing your news! Our unique digital approach enables us to circulate your...

Frank Vizesi

Theradaptive, the market leader in targeted regenerative therapeutics, today announced the expansion of its senior leadership team with the appointment of Dr. Frank Vizesi, Ph.D. as Chief Scientific Officer.

Frank joins from Orthofix, where he was Chief Scientific Officer, and brings over two decades of experience in orthobiologics and spinal fusion.  He is a highly respected biomedical scientist who has been at the forefront of spinal fusion research throughout his career. He is passionate about driving progress in the field and bringing new technologies to surgeons that deliver improved outcomes for patients.

“I have dedicated my career to developing the best solutions for spinal fusion, and I am delighted to be part of a team that is developing by far the most exciting innovation I have seen in the space,” said Dr. Frank Vizesi, Chief Scientific Officer at Theradaptive. “Theradaptive has the potential to transform the standard of care with OsteoAdapt, and I am looking forward to working with the team to build the clinical data and scientific evidence we need to bring OsteoAdapt SP to patients in the clinic in the shortest timeframe possible.”

Dr. Luis Alvarez, Theradaptive Founder and CEO

“Frank’s deep experience in orthobiologics and spinal fusion is an incredible asset for Theradaptive and will be game-changing as we continue to transform into a clinical-stage organization. He shares our passion for unlocking the vast potential of targeted therapeutic proteins and we are delighted to have him on board for the next stage of Theradaptive’s journey as we progress in spinal fusion and continue to demonstrate the wider applications of our protein engineering platform in an increasing number of disease areas.”

Frank Vizesi is a natural leader, and his experience will be invaluable in shaping and guiding the industry-leading clinical and scientific team at Theradaptive as it continues to expand with the business. His initial priority will be working alongside the clinical and regulatory team to aid in the successful execution of the OsteoAdapt clinical study program and navigate the path to U.S. Food & Drug Administration (F.D.A.) approval, bringing this groundbreaking new approach to patients. Frank will also support Theradaptive’s ongoing label expansion into sports medicine, dental, and craniomaxillofacial indications using their clinical-stage AMP2 asset.

A GROWING NEED FOR TREATMENT INNOVATION

There is an increasingly urgent need for therapeutic advances in the spinal fusion landscape, as the demand for spinal fusion surgery continues to increase in line with our aging population. 40% of adults over 40 have at least one degenerated disc and this proportion rises to 80% in adults aged 80 and over. Currently 1 in 6 Americans is over 65, representing a huge and growing population of people living with spinal degeneration.

A UNIQUE APPROACH

Theradaptive is on a mission to unlock the vast potential of protein therapeutics to meet urgent patient unmet needs. Its unique protein engineering platform takes existing therapeutic proteins and create variants that are material-binding, or ‘sticky’, allowing them to be applied to the surface of an implant or device, like a coat of paint. This gives surgeons significantly greater control around where the protein is placed and how it behaves in the body, overcoming many of the current challenges associated with the clinical use of therapeutic proteins.

Its lead product, OsteoAdapt SP, is a spinal fusion implant coated in a layer of a powerful bone formation protein called AMP-2, making its entire surface bioactive. Once placed at the site of fusion, AMP-2 cannot disperse away and is readily available to trigger the cellular pathways that drive bone formation. OsteoAdapt SP has been awarded three breakthrough device designations by the U.S. F.D.A., and the first global clinical study to assess its effectiveness and safety in spinal fusion began in April 2024.

Medical Device News Magazinehttps://infomeddnews.com
Medical Device News Magazine provides breaking medical device / biotechnology news. Our subscribers include medical specialists, device industry executives, investors, and other allied health professionals, as well as patients who are interested in researching various medical devices. We hope you find value in our easy-to-read publication and its overall objectives! Medical Device News Magazine is a division of PTM Healthcare Marketing, Inc. Pauline T. Mayer is the managing editor.

Other News

Shoulder Innovations Further Strengthens IP Portfolio in Key Areas with Recent Patent Grants

"These recent grants further strengthen key patent families that are foundational to our technology, and we are pleased the USPTO continues to recognize our meaningful innovation in the shoulder arthroplasty segment," said Rob Ball, CEO of Shoulder Innovations. "This noteworthy expansion of our IP position represents the culmination of over 10 years of research and development, and we are proud of our team for their continued dedication to creating practical solutions for shoulder surgeons and advancing patient outcomes."

Radical Catheter Technologies Presents Analysis of Disruptive, Recently FDA-Cleared Endovascular Technology at the Society of NeuroInterventional Surgery 21st Annual Meeting

This new catheter, the first product commercialized from this novel technology platform, is designed to enable access to the blood vessels in the brain for both femoral and radial access. A multi-center analysis of this disruptive technology is being presented today at Society of NeuroInterventional Surgery 21st annual meeting. In addition, the Company confirmed the closing of a $20 million financing round led by NeuroTechnology Investors, which will be used to scale the company and expand the Radical platform notes Radical Catheter Technologies.

Rapid Medical™ Completes Initial Neurovascular Cases in the USA Following FDA Clearance of Its Active Access Solution

“With DRIVEWIRE, our design goal was to bring new levels of access and control to the interventional suite while improving best-in-class guidewires,” comments Giora Kornblau, Chief Technology Officer at Rapid Medical. “When physicians are looking for technologies that increase the clinical possibilities and safety for the patient, we want Rapid to be the first place they look.”