RevBio Teams with NIH for Groundbreaking Clinical Trial Grant
RevBio Secures $2.4 Million Grant for Clinical Innovation
Lowell, Massachusetts – RevBio, Inc. proudly announces that it has received a significant $2.4 million grant from the National Institutes of Health (NIH) to support its innovative regenerative bone adhesive, TETRANITE. This milestone grant is part of the Phase II Small Business Innovation Research (SBIR) initiative designed to accelerate advancements in medical technology.
Understanding TETRANITE
TETRANITE is a cutting-edge injectable bone adhesive intended for use in various surgical applications, particularly to enhance stabilization during brain surgery procedures. The awarded funding will facilitate a comprehensive clinical trial focusing on the safety and effectiveness of this unique biomaterial, specifically for cranial flap fixation.
Clinical Trial Insights
This clinical trial, already approved by the FDA, is set to involve 20 patients, with five enrolled so far. The study is being conducted at prominent institutions, including the Semmes Murphey Clinic and Brigham and Women’s Hospital. Initial feedback has been encouraging, with signs of effective healing reported in early participants.
The Role of TETRANITE in Surgery
Dr. L. Madison Michael, a prominent neurosurgeon participating in the trial, has expressed optimism about the early outcomes. According to Dr. Michael, the healing process has been notably positive, with radiographic imaging confirming the secure adhesion of bone flaps to the skull. This breakthrough could pave the way for a shift in surgical practices regarding cranial surgeries.
The Benefits of Improved Bone Adhesives
Modern surgical techniques, combined with advancements like TETRANITE, are enhancing patient recovery experiences significantly. Dr. Timothy R. Smith emphasizes that robust healing solutions like TETRANITE not only help physically but also boost patients' emotional well-being following major surgeries.
RevBio’s Vision and Future Prospects
Founded with a mission to enhance surgical outcomes, RevBio is focused on innovative medical solutions that can transform patient care. TETRANITE represents just one facet of the company’s wider objectives, investing heavily in research to expand into other markets such as dentistry and orthopedics.
About RevBio, Inc.
RevBio, Inc. stands at the forefront of medical device development, primarily focusing on pioneering synthetic biomaterials. TETRANITE is designed to be self-setting and osteoconductive, amplifying its use within the healthcare landscape. As a clinical stage company, RevBio is committed to ensuring that its groundbreaking technologies receive the necessary approvals for safe and effective commercial use.
Frequently Asked Questions
What is TETRANITE, and how does it work?
TETRANITE is a synthetic, injectable bone adhesive designed for surgical applications, specifically for cranial flap fixation.
How much funding has RevBio received for the clinical trial?
RevBio has secured a $2.4 million grant from the NIH to support its clinical trial.
Where is the clinical trial being conducted?
The clinical trial is taking place at the Semmes Murphey Clinic and Brigham and Women’s Hospital.
Has the clinical trial received any approvals?
Yes, the clinical trial has been approved by the FDA.
What other markets does RevBio plan to enter?
RevBio is exploring applications in dentistry, orthopedics, and animal health markets.
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