As this is the first time the implant is being tested in humans, the team are initially recruiting six patients with damage to their knee joint cartilage. This first phase of the study will investigate the implant’s safety and performance in patients. It will also evaluate the instrument set used to implant FibroFix™ in the joint. If successful, the next phase of the trial will recruit a larger group of patients to understand how well the implant performs.
FibroFix™ is made of a protein extracted from silk and has a porous structure. It acts as a scaffold for new cartilage tissue to grow around it. Both the implant and instrument set have been robustly assessed according to the Medicines and Healthcare products Regulatory Agency (MHRA) standards, allowing the implant to be tested in humans for the first time.
Cartilage is a flexible layer of tissue that acts as a shock absorber in the knee. It can be damaged through sudden injury or gradual deterioration such as seen in osteoarthritis.
Nick Howells, principal investigator and consultant knee surgeon at Southmead Hospital, North Bristol NHS Trust, said: “This implant has great potential to help patients with symptoms from localised areas of cartilage damage in the knee. It is the culmination of a huge amount work to have now reached the stage of a clinical trial and very exciting for us to be able to start to trial the use of the implant in patients. This will focus on safety first and once we have confirmed this will hopefully evolve into the assessment of clinical performance.”
FFLEX study chief investigator, Michael Whitehouse, Professor of Trauma & Orthopaedics at the University of Bristol and NIHR Bristol Biomedical Research Centre (Bristol BRC), said: “This technology represents the culmination of a huge amount of development of the implant and the associated instruments to allow a reliable and reproducible operation. It potentially fills a gap in current available treatments. It would allow the treatment of immediate pain and limited function for patients with focal cartilage problems. Typically, operations for these problems are technique dependent or require prolonged periods of limited weightbearing or restricted activity. The instruments developed for this implant and the implant itself provide very strong fixation during the course of the operation and allow an early return to normal activity. Successful treatment of focal cartilage lesions may help to reduce the risk of more widespread joint damage in the future.”
Nick Skaer, co-founder and CEO of Orthox, said: “FibroFix is unique in emulating the functional properties of cartilage while also, in laboratory tests, facilitating rapid tissue regeneration. It could make a real difference to patients suffering the debilitating effects of serious knee cartilage injuries. With our approach there is significant bone sparing and strong tissue integration of the implant, which we hope may result in faster recovery. NIHR’s funding for the FFLEX study is just one of several grants we’ve received to test FibroFix internationally. We hope this paves the way for a significant number of patients to be treated with our FibroFix implants every year.”
