LaunchPad Medical Receives Approval to Start a Clinical Trial in the United Kingdom to Study its Bone Adhesive Biomaterial in the Field of Implant Dentistry

Friday, August 7, 2020

LaunchPad Medical, Inc. announced that it has received approval from the Medicines and Healthcare products Regulatory Agency in the United Kingdom to start a 15-patient pilot clinical study to examine the safety and efficacy of Tetranite®, the company’s bone adhesive biomaterial, to immediately stabilize dental implants following tooth extractions.

This study will focus specifically on anterior teeth located in the aesthetic or “smile” region where the loss of a tooth is highly visible. Unlike the company’s ongoing clinical study in the United States, patients in this study will receive temporary crowns at the time their implants are placed.  The use of Tetranite will obviate a costly, complex, and lengthy bone grafting process for many patients, greatly accelerating the overall treatment timeframe.

Dr. Michael R. Norton, BDS, FDS, RCS(Ed), a London-based oral surgeon, noted lecturer, and former President of the international Academy of Osseointegration, will serve as the chief investigator for this study. “I am thrilled to be the first clinician outside the United States to use this ground-breaking technology to improve the care of my patients and accelerate the restoration of their dentition,” said Dr. Norton. “I believe this technology will revolutionize the way we place dental implants.”

“We are extremely excited to initiate our first study outside the United States,” said Brian Hess, CEO of LaunchPad Medical, “and we are very pleased to be working with Dr. Norton who is a thought leader in advancing clinical practice in the field of implant dentistry.”

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